Open Access

Evaluation of normalization methods for cDNA microarray data by k-NN classification

  • Wei Wu1, 2Email author,
  • Eric P Xing3,
  • Connie Myers1,
  • I Saira Mian1 and
  • Mina J Bissell1
BMC Bioinformatics20056:191

DOI: 10.1186/1471-2105-6-191

Received: 17 December 2004

Accepted: 26 July 2005

Published: 26 July 2005

Abstract

Background

Non-biological factors give rise to unwanted variations in cDNA microarray data. There are many normalization methods designed to remove such variations. However, to date there have been few published systematic evaluations of these techniques for removing variations arising from dye biases in the context of downstream, higher-order analytical tasks such as classification.

Results

Ten location normalization methods that adjust spatial- and/or intensity-dependent dye biases, and three scale methods that adjust scale differences were applied, individually and in combination, to five distinct, published, cancer biology-related cDNA microarray data sets. Leave-one-out cross-validation (LOOCV) classification error was employed as the quantitative end-point for assessing the effectiveness of a normalization method. In particular, a known classifier, k-nearest neighbor (k-NN), was estimated from data normalized using a given technique, and the LOOCV error rate of the ensuing model was computed. We found that k-NN classifiers are sensitive to dye biases in the data. Using N ONRM and GMEDIAN as baseline methods, our results show that single-bias-removal techniques which remove either spatial-dependent dye bias (referred later as spatial effect) or intensity-dependent dye bias (referred later as intensity effect) moderately reduce LOOCV classification errors; whereas double-bias-removal techniques which remove both spatial- and intensity effect reduce LOOCV classification errors even further. Of the 41 different strategies examined, three two-step processes, IG LOESS-SL FILTERW7, IST SPLINE-SL LOESS and IG LOESS-SL LOESS, all of which removed intensity effect globally and spatial effect locally, appear to reduce LOOCV classification errors most consistently and effectively across all data sets. We also found that the investigated scale normalization methods do not reduce LOOCV classification error.

Conclusion

Using LOOCV error of k-NNs as the evaluation criterion, three double-bias-removal normalization strategies, IG LOESS-SL FILTERW7, IST SPLINE-SL LOESS and IG LOESS-SL LOESS, outperform other strategies for removing spatial effect, intensity effect and scale differences from cDNA microarray data. The apparent sensitivity of k-NN LOOCV classification error to dye biases suggests that this criterion provides an informative measure for evaluating normalization methods. All the computational tools used in this study were implemented using the R language for statistical computing and graphics.

Background

Molecular profiling technology allows for the simultaneous assaying of the abundance of tens of thousands of transcripts in a biological sample. Once these abundance values have been obtained for many samples, prevalent higher-order data analyses may include clustering, classification, feature selection, and network estimation. A variety of algorithms seeking to address these higher-order tasks have been investigated and applied, to interpret gene expression patterns and to generate biological predictions. However, the accuracy of these predictions may depend on the low-level transformations utilized to produce abundance values from raw measurements, i.e., data pre-processing may be a critical factor in determining the validity and success of downstream studies. Some key pre-processing steps for profiling data include image quantification and normalization. Several image analysis software (e.g., GenePix and SPOT) have been designed for image analysis of the spots on microarrays [1, 2]. Background estimation has also been considered as an important issue in image quantification, however, evidence [2, 3] showed that 'inappropriate' local background adjustment could add noise into the microarray data and thus be detrimental to the downstream studies. Background adjustment, therefore, is still an issue to be resolved. After image analysis, normalization usually needs to be performed. It is a procedure designed to minimize the unwanted variations in measurements arising from the technology, but to retain the intrinsic biological variations, and is also the focus of this work. In this study, we examined normalization in the context of a particular transcriptional profiling platform, cDNA microarrays [46], and the specific analytical task of classifying biological samples characterized by gene expression profiles.

In cDNA microarray-based investigations, RNA from two samples are reverse-transcribed and labeled with distinct (red and green) fluorescent dyes, then hybridized to a microarray spotted with DNA sequences ("probes"). An ensuing scanned image of the microarray is processed to yield an intensity measurement for each dye at every spot (Figure 1). If R and G are the spot-specific, quantitated, fluorescent intensities of the target and reference expression signals respectively, relative gene expression is defined as the log ratio M = log2(R / G), and average expression is the log intensity https://static-content.springer.com/image/art%3A10.1186%2F1471-2105-6-191/MediaObjects/12859_2004_Article_516_IEq1_HTML.gif . Based on different biological assumptions and design principles, many normalization methods for cDNA microarray data have been proposed. Global normalization techniques adjust the center (e.g., mean or median) of the distribution of the log ratio M values on each microarray to a constant [1, 79]. These methods, however, do not correct for any intensity- or spatial effect.
https://static-content.springer.com/image/art%3A10.1186%2F1471-2105-6-191/MediaObjects/12859_2004_Article_516_Fig1_HTML.jpg
Figure 1

A scanned image of an illustrative cDNA microarray. The configuration (layout of spots) can be described via a previously defined notation encompassing four numbers (ngr, ngc, nsr, nsc) [12]. A print-tip (PT) group is a set of spots arranged in a grid with "nsr" rows and "nsc" columns. A microarray is a set of PT groups arranged in a pattern of "ngr" rows and "ngc" columns. The configuration of the microarray shown is (ngr = 2, ngc = 2, nsr = 24, nsc = 24), i.e., 2 × 2 PT groups each composed of 24 × 24 spots. The terms "local" and "global" level refer to the spots in a PT group and the entire microarray respectively.

A variety of techniques have been proposed to remove intensity effect. A non-linear approach employs robust locally weighted regression (lowess) [10] to smooth the dependence of log ratios on intensities [4, 11, 12]. The basic assumption of this approach is either that the majority of genes are not differentially expressed, or that genes are influenced by random effects (i.e., the numbers of up-regulated and down-regulated genes are similar) [4, 11, 12]. A 'qspline' method uses a target array to adjust R and G values so that their distribution is similar for all arrays [13], but the performance of this method may depend upon the choice of the baseline array [14]. A composite method employs both external control samples and total genes on a microarray to remove intensity effect [15]. To relax critical biological assumptions, 'housekeeping-gene'-related methods first identify non-differentially-expressed genes, and then use these genes for normalization [1618]. Semi-linear models are designed to account for the effects of print-tips (PTs), signal intensity, and differences in gene expression levels jointly in a single model [19, 20].

The removal of intensity effect at the PT level can partially remove spatial effect [4, 11]. To remove spatial effect more completely, the dependence of M values on physical position can be smoothed using lowess [12], or can be eliminated using weighted mean [13] or median filter methods [17], both of which assume that differentially expressed genes are not co-localized in the neighboring spots. Since spatial- and intensity effect may be mutually dependent, a method that removes global spatial effect and global intensity effect in a single step has been proposed [21].

Whereas the above location normalization methods remove spatial- and intensity effect, scale normalization methods adjust differences in the scale of M values within and/or between microarrays. The assumption is that since the majority of genes are not differentially expressed, the scale of their M values should be constant. A robust estimate of the scale factor for scale normalization is median absolute deviation [15].

Normalization approaches seek to ensure that dye effect is removed, while biological variations are retained. Spatial- and intensity effect and scale effect arise from printing, hybridization, scanning, or other technical factors, and can mask the signals arising from genuine biological variations in gene expression. Visual aids used to assess the effectiveness of normalization methods [11, 13, 15, 21] include scatter plots of log ratio (M) versus average log intensity (A) ("MA plots"). Spatial plots are a color-coded representation of each spot on a microarray that depicts M values, or a quality (e.g., shape, size) measure of some test statistic. These two types of diagnostic plots [4, 21] suggest that raw M values are often biased estimates of relative expression and that the dye intensities per spot need to be adjusted. Quantitative criteria used to assess the robustness of normalization methods in removing dye effect include (i) rank variations of spot intensity in non-normalized versus normalized data [9, 22], and (ii) correlation [16, 21], variance [8, 13], or error [18, 22] of the normalized M values in replicated data.

To ensure that biological variations are retained after normalization, several functional criteria have been employed. Prevailing approaches determine the ability to predict a fixed number of differentially expressed genes in real or simulated data using quantitative measures based on t-statistics [4, 11, 13, 21], adjusted p-values [11], and false-discovery rates [23]. However, there is uncertainty associated with these measures, and the true number of differentially expressed genes is unknown. Spike-in data have been used to assess normalization approaches for Affymetrix GeneChip data [14, 24, 25]. However, external control samples are not widely used for evaluation of normalization methods for cDNA microarrays.

In this paper, we evaluated normalization methods for cDNA microarray data using the k-NN LOOCV classification error (of biological samples characterized by the gene expression profiles), an alternative quantitative functional measure that is relatively unambiguous, objective and readily computed. We used k-NN classifiers because (i) their sensitivity enables us to discriminate between, and hence evaluate normalization techniques, (ii) they are readily available, (iii) they perform well in practice, and (iv) their non-parametric nature means that assumptions about how the data are distributed have little influence on classification performance. Since the primary aim of our evaluation of normalization methods was to assist practitioners in choosing effective data pre-processing schemes, we did not consider factors that may influence classification performance, such as feature selection and distance metrics. We investigated a wide spectrum of well-known and widely available normalization techniques: ten location normalization methods that adjust spatial effect and/or intensity effect (Table 1), and three scale methods that adjust scale differences (Table 3). We applied these methods, individually and in combination (41 strategies in all, Tables 1, 2, 3), to five diverse, published, cancer biology-related cDNA microarray data sets (Table 4), and we generated data sets with spatial effect, intensity effect and scale differences removed to varying degrees. Computing the LOOCV classification error of k-NNs estimated from these multi- and two-class data sets allowed us to investigate which and how much of the dye effect are removed by the 41 strategies.
Table 1

Single-bias-removal location normalization techniques used in this study. These strategies remove spatial- or intensity effect in a single step. The abbreviations are as follows, (for a given microarray), M l : location-normalized log ratio; median(M): median value of non-normalized log ratios; lowess(rloc i , cloc i ): lowess curve fitted as a function of the row location (rloc i ) and column location (cloc i ) of spots in PT group i; median(M w ): median value of non-normalized log ratios within the window size determined by w; lowess(A): lowess curve fitted to an MA plot of spots on a microarray; lowess(A i ): lowess curve fitted to an MA plot of spots in PT group i; spline(A iset ): spline curve fitted to an MA plot of spots in the invariant set, iset; R l : location-normalized R value; qspline(G i ): qspline smoothing using geometric mean of the G channels of all arrays as a target array; G l : location-normalized G value; qspline(R t ): qspline smoothing using geometric mean of the R channels of all arrays as a target array.

Name *

Description: Effect/Level

Bioconductor R package/function(parameters)

N ONRM

No normalization M l = M

marray/maNorm(norm="none")

GMEDIAN

Global M l = M - median(M)

marray/maNorm (norm="median", subset = T)

SL LOESS

Spatial/local lowess M l = M - loess(rloc i , cloc i )

marray/maNormMain (f.loc = list(maNorm2D(g="maPrintTip", subset = T, span = 0.4))

SL FILTERW3

Spatial/Local median filter

M l = M - median(M w ), W = 3 × 3

tRMA/SpatiallyNormalise** (M, width = 3, height = 3)

SL FILTERW7

Spatial/Local median filter

M l = M - median(M w ), W = 7 × 7

tRMA/SpatiallyNormalise** (M, width = 7, height = 7)

IG LOESS

Intensity/Global lowess M l = M - loess(A)

marray/maNorm (norm="loess", subset = TRUE, span = 0.4)

IL LOESS

Intensity/Local lowess M l = M - loess(A i )

marray/maNorm (norm="printTipLoess", subset = T, span = 0.4)

IST SPLINE

Intensity/Global spline M l = M - spline(A iset )

affy/normalize.invariantset**(prd.td = c(0.003, 0.007))

QSPLINEG

Intensity/Global qspline

R l = R - qspline(G t ), G l = G - qspline(G t ), M l = log(R l / G l )

affy/R l ← normalize.qspline(R, 2^rowMeans(log2(G), na.rm = T), na.rm = T, *default*)

G l ← normalize.qspline(G, 2^rowMeans(log2(G), na.rm = T), na.rm = T, *default*)

QS PLINER

Intensity/Global qspline

R l = R - qspline(R t ), G l = G - qspline(R t ), M l = log(R l / G l )

affy/ R l ← normalize.qspline(R, 2^rowMeans(log2(R), na.rm = T), na.rm = T, *default*)

G l ← normalize.qspline(G, 2^rowMeans(log2(R), na.rm = T), na.rm = T, *default*)

* We adopted the terminology given in the table to avoid confusion within this work. Elsewhere, these methods are known as: GMEDIAN, global or median [4]; SL LOESS, 2D spatial [12]; SL FILTERW3, spatial normalization using median filter of the block size 3 × 3 [17]; SL FILTERW7, spatial normalization using median filter of the block size 7 × 7 [17]; IG LOESS, global loess [4, 26]; IL LOESS, print-tip loess [4]; IST SPLINE, invariant set normalization [38]; QS PLINER, qspline using geometric mean of the R channels of all arrays as the target array [13]; Q SPLINEG, qspline using geometric mean of the G channels of all arrays as the target array [13].

** The SpatiallyNormalise function in the tRMA package was modified to remove scale normalization. The normalize.invariantset function in Affy package was modified so that the function could be applied on cDNA microarray data.

*default* The default parameters for Q SPLINEG and QS PLINER are (fit.iters = 5, min.offset = 5, spline.method="natural", smooth = T, spar = 0, p.min = 0, p.max = 1.0, incl.ends = T, converge = F)

Table 2

Double-bias-removal location normalization techniques used in this study. These strategies remove both spatial- and intensity effect either in a single step (IG SG LOESS) or in two steps (the remaining thirteen approaches) by combining methods listed in Table 1.

Name

Description: Method/Effect/Level

IG SG LOESS*

Joint Intensity/Global & Spatial/Global M l = M - lowess(A, rloc, cloc)

IG LOESS-SL LOESS

Step 1: IG LOESS/Intensity/Global lowess

Step 2: SL LOESS/Spatial/Local lowess

IL LOESS-SL LOESS

Step 1: IL LOESS/Intensity/Local lowess

Step 2: SL LOESS/Spatial/Local lowess

IG LOESS-SL FILTERW3

Step 1: IG LOESS/Intensity/Global lowess

Step 2: SL FILTERW3/Spatial/Local median filter

IG LOESS-SL FILTERW7

Step 1: IG LOESS/Intensity/Global lowess

Step 2: SL FILTERW7/Spatial/Local median filter

IST SPLINE-SL LOESS

Step 1: IST SPLINE/Intensity/Global spline

Step 2: SL LOESS/Spatial/Local lowess

IST SPLINE-SL FILTERW3

Step 1: IST SPLINE/Intensity/ Global spline

Step 2: SL FILTERW3/Spatial/Local median filter

IST SPLINE-SL FILTERW7

Step 1: IST SPLINE/Intensity/Global spline

Step 2: SL FILTERW7/Spatial/Local median filter

Q SPLINEG-SL LOESS

Step 1: Q SPLINEG/Intensity/Global qspline

Step 2: SL LOESS/Spatial/Local lowess

Q SPLINEG-SL FILTERW3

Step 1: Q SPLINEG/Intensity/Global qspline

Step 2: SL FILTERW3/Spatial/Local median filter

Q SPLINEG-SL FILTERW7

Step 1: Q SPLINEG/Intensity/Global qspline

Step 2: SL FILTERW7/Spatial/Local median filter

QS PLINER-SL LOESS

Step 1: QS PLINER/Intensity/Global qspline

Step 2: SL LOESS/Spatial/Local lowess

QS PLINER-SL FILTERW3

Step 1: QS PLINER/Intensity/Global qspline

Step 2: SL FILTERW3/Spatial/Local median filter

QS PLINER-SL FILTERW7

Step 1: QS PLINER/Intensity/Global qspline

Step 2: SL FILTERW7/Spatial/Local median filter

* IG SG LOESS was implemented in the following package/function: MAANOVA R package/smooth (method="rlowess", f = 0.4, degree = 2). Elsewhere, IG SG LOESS is known as joint loess [21]. lowess(A, rloc, cloc): lowess curve fitted as a function of average log intensity (A), row location (rloc), and column location (cloc) of spots on a microarray.

Table 3

Extant scale normalization techniques used in this study. For a given microarray, if M l is a location-normalized log ratio, then M s is the scale-normalized log ratio, where M s = M l / s, and s is median absolute deviation from the median (MAD), a robust estimate of the scale of the data distribution. The remaining abbreviations are as follows, median(M l ): median value of M l values of spots on all microarrays in a data set; https://static-content.springer.com/image/art%3A10.1186%2F1471-2105-6-191/MediaObjects/12859_2004_Article_516_IEq2_HTML.gif : median value of M l values of spots in PT group i on a microarray.

Name *

Description

Bioconductor R package/function (parameters)

W SCALE

Within-microarray scale normalization https://static-content.springer.com/image/art%3A10.1186%2F1471-2105-6-191/MediaObjects/12859_2004_Article_516_IEq3_HTML.gif

M s = M l / s i

marrayNorm/maNormScale (norm="printTipMAD", subset = T, geo = T, Mscale = T)

B SCALE

Between-microarray scale normalization

s = median(M l - median(M l ))

M s = M l / s

marrayNorm/maNormScale (norm="globalMAD", subset = T), geo = T, Mscale = T)

WB SCALE

Step 1: Within-microarray scale normalization https://static-content.springer.com/image/art%3A10.1186%2F1471-2105-6-191/MediaObjects/12859_2004_Article_516_IEq3_HTML.gif

https://static-content.springer.com/image/art%3A10.1186%2F1471-2105-6-191/MediaObjects/12859_2004_Article_516_IEq4_HTML.gif

marrayNorm/maNormScale (norm="printTipMAD", subset = T, geo = T, Mscale = T)

 

Step 2: Between-microarray scale normalization

s = median(M l - median(M l ))

https://static-content.springer.com/image/art%3A10.1186%2F1471-2105-6-191/MediaObjects/12859_2004_Article_516_IEq5_HTML.gif

marrayNorm/maNormScale (norm="globalMAD", subset = T, geo = T, Mscale = T)

* We adopted the terminology given in this table to avoid confusion within this work. Elsewhere, the methods are known as: W SCALE, within-print-tip-group scale normalization [4]; and B SCALE, between slide scale normalization [4, 15].

Table 4

The multi-class, cancer-biology related transcriptional profiling data sets analyzed in this work. For each of the five published studies, the fluorescent intensities, microarray images, and associated information were downloaded from the URLs indicated. The statistics refer to data sets produced after application of all pre-normalization data processing, location/scale normalization, and post-normalization data processing steps. The abbreviations are as follows, Microarrays: number of cDNA microarrays; Probes: number of probes; K: total number of categories to which a sample could be assigned; Samples and Class: number of samples in the specified pre-defined category; Configuration: configuration of a microarray using the convention described in Figure 1.

Data set name

Description

LIVER CANCER [46]

Microarrays: 181; Probes: 6,605; K = 2

Samples and Class: 76 normal; 105 tumor

Configuration: (ngr = 8, ngc = 4, nsr = 27, nsc = 28)

http://​genome-www5.​stanford.​edu/​cgi-bin/​publication/​viewPublication.​pl?​pub_​no=​107

LYMPHOMA [47]

Microarrays: 81; Probes: 6,850; K = 3

Samples and Class: 29 normal, 43 diffuse large B-cell lymphoma (DLBCL); 9 follicular lymphoma (FL)

Configuration: (ngr = 4, ngc = 4, nsr = 24, nsc = 24); (ngr = 8, ngc = 4, nsr = 24, nsc = 24)

http://​genome-www5.​stanford.​edu/​cgi-bin/​publication/​viewPublication.​pl?​pub_​no=​79

RENAL CELL CARCINOMA [48]

Microarrays: 38; Probes: 13,608; K = 4

Samples and Class: 3 normal; 26 clear cell carcinoma (CCC); 5 granular cell carcinoma (GCC);

4 papillary carcinoma (PC)

Configuration: (ngr = 8, ngc = 4, nsr = 27, nsc = 28)

http://​genome-www5.​stanford.​edu/​cgi-bin/​publication/​viewPublication.​pl?​pub_​no=​210

GASTRIC CARCINOMA [49]

Microarrays: 130; Probes: 15,541; K = 2

Samples and Class : 28 normal; 102 tumor

Configuration: (ngr = 12, ngc = 4, nsr = 30, nsc = 32); (ngr = 12, ngc = 4, nsr = 29, nsc = 32);

(ngr = 12, ngc = 4, nsr = 30, nsc = 30)

http://​genome-www5.​stanford.​edu/​cgi-bin/​publication/​viewPublication.​pl?​pub_​no=​232

LUNG CANCER [50]

Microarrays: 60; Probes: 20,601; K = 5

Samples and Class: 6 normal; 35 adenocarcinoma (AC); 11 squamous cell carcinoma (SCC);

4 large cell lung cancer (LCLC); 4 small cell lung cancer (SCLC)

Configuration: (ngr = 8, ngc = 4, nsr = 27, nsc = 28)

http://​genome-www5.​stanford.​edu/​cgi-bin/​publication/​viewPublication.​pl?​pub_​no=​100

Results

Spatial- and intensity-dependent normalization

Diagnostic plots

We used diagnostic plots to examine the ability of different location normalization methods to remove spatial- and/or intensity effect (Tables 1 and 2). Figure 2 shows spatial plots for two specific LYMPHOMA microarrays normalized with four approaches designed to correct spatial effect (SL LOESS, SL FILTERW3, SL FILTERW7, IG SG LOESS). The non-normalized M values (N ONRM) for microarray "5850" display global spatial effect (left-to-right, green-to-red pattern) whereas those for microarray "5938" exhibit local spatial effect (top-to-bottom, green-to-red pattern in each PT group). Removal of spatial effect should result in a "random" red and green pattern of M values. SL LOESS and SL FILTERW7 exhibit similar dye bias-removal abilities in that they both remove global spatial effect more effectively than local spatial effect. SL FILTERW3 removes both global and local dye effect effectively, largely because it uses a median filter of a small window size (3 × 3 spots) for normalization. IG SG LOESS removes most, but not all, global and local spatial effect (a strip of red spots on the right side of "5850" and on the bottom of the PT groups in the first row of "5938" remain). IG SG LOESS may not be as effective at removing dye effect as expected because, as the developers indicate, lowess curve construction uses the standardized spatial variables (rloc, cloc), which may not be appropriate for location variables [21].
https://static-content.springer.com/image/art%3A10.1186%2F1471-2105-6-191/MediaObjects/12859_2004_Article_516_Fig2_HTML.jpg
Figure 2

Spatial plots of microarrays 5850 and 5938 in the Lymphoma data set. Spatial plots of microarrays 5850 and 5938 in the LYMPHOMA data set. The plots show the results before and after location normalization designed to remove spatial effect. The spatial plot is a spatial representation of spots on the microarray color-coded by their M values (marrayPlots/maImage(x="maM", subset = T)). Spots in white are spots flagged in the original microarray data (missing values). Rows depict non-normalized (N ONRM), and normalized M l values (SL LOESS, SL FILTERW3, SL FILTERW7, IG SG LOESS).

Figure 3 shows intensity-dependent MA plots for one specific LYMPHOMA microarray overlaid with one lowess curve (left) or one lowess curve per print tip group (right) using six methods designed to correct intensity effect (IG LOESS, IL LOESS, IST SPLINE, Q SPLINEG, QS PLINER, IG SG LOESS). For non-normalized M values (N ONRM), the curvature in the MA plot indicates the presence of intensity effect at the array (left) and PT (right) level. All six methods remove global intensity effect completely (flat lowess curves, left), but only IL LOESS and IG SG LOESS remove local intensity effect thoroughly (right).
https://static-content.springer.com/image/art%3A10.1186%2F1471-2105-6-191/MediaObjects/12859_2004_Article_516_Fig3_HTML.jpg
Figure 3

MA plots of microarray 5812 in the LYMPHOMA data set. The plots show the results before and after location normalization designed to remove intensity effect. The MA plot is a scatter plot of log ratio M = log2(R f / G f ) (abscissa) versus average log intensity https://static-content.springer.com/image/art%3A10.1186%2F1471-2105-6-191/MediaObjects/12859_2004_Article_516_IEq6_HTML.gif (ordinate). Columns depict non-normalized (N ONRM), and normalized M l values (IG LOESS, IL LOESS, IST SPLINE, Q SPLINEG, QS PLINER, IG SG LOESS). Plots in the same row represent same data except that each plot in the left panel shows one lowess curve for all the spots (marrayPlots/maPlot(data, z = NULL)); while that in the right panel shows one lowess curve per PT group (marrayPlots/maPlot(x="maA", y="maM", z="maPrintTip")). Different colors and line types are used to represent different groups from different rows ("ngr", Figure 1) and columns ("ngc") respectively.

Visual inspection of the diagnostic plots in Figures 2 and 3 suggest that SL FILTERW3 is an effective method for removing both global and local spatial effect, whereas IL LOESS is good at removing intensity effect.

k-NN LOOCV Classification error

For a functional, quantitative evaluation of location normalization methods, we first computed k-NN LOOCV classification error rates for data normalized using these methods individually and/or in combination. Then for each data set, we ranked the normalization methods based on their LOOCV classification error rates. The smaller the LOOCV classification error rate, the lower the rank of the normalization strategy. In order to assess whether normalization is beneficial (or not), we also computed the following quantity for a normalization method in each data set:

IMPROVEMENT = (ErrorRate(N ONRM) - ErrorRate(Method)) / ErrorRate(N ONRM) × 100%

where ErrorRate(N ONRM) is the error rate of N ONRM, and ErrorRate(Method) is the error rate of the method. Tables 5 and 6 give results for five data sets (Table 4) and 23 location methods designed to remove spatial- and/or intensity effect (Tables 1 and 2). Figures 4 and 5 are alternative, visual representations of the classification "Error Rate" and "Rank" in Table 5.
Table 5

Leave-one-out cross-validation k-NN error rates for location normalized data. For each data set, the normalization methods were ranked based on their LOOCV classification error rates ("Rank"). The smaller the LOOCV classification error rate, the lower the rank. The methods are arranged in the following order: single-bias-removal methods (block 1), double-bias-removal methods (block 2) and the qspline-related methods (block 3). For a given data set, the smallest error rate(s) and rank(s) are shown in bold. The methods and data sets are described in Tables 1, 2 and 4, respectively.

Location Normalization method

LIVER CANCER

LYMPHOMA

RENAL CELL CARCINOMA

GASTRIC CARCINOMA

LUNG CANCER

 

Error Rate

Rank

Error Rate

Rank

Error Rate

Rank

Error Rate

Rank

Error Rate

Rank

N ONRM

0.202

24

0.266

23

0.237

24

0.0347

24

0.359

23.5

GMEDIAN

0.163

21

0.247

21

0.158

22

0.0270

23

0.342

20.5

SL LOESS

0.136

9.5

0.272

24

0.132

16.5

0.0154

12

0.350

22

SL FILTERW3

0.155

16

0.216

20

0.132

16.5

0.0190

14

0.359

23.5

SL FILTERW7

0.144

12.5

0.253

22

0.132

16.5

0.0228

16

0.325

17.5

IG LOESS

0.133

8

0.186

15.5

0.132

16.5

0.0231

20

0.342

20.5

IL LOESS

0.110

2

0.154

13

0.132

16.5

0.0231

20

0.275

12.5

IST SPLINE

0.129

7

0.177

14

0.114

7

0.0153

10

0.334

19

IG SG LOESS

0.136

9.5

0.130

10

0.132

16.5

0

2

0.283

15

IG LOESS-SL LOESS

0.113

3.5

0.117

6.5

0.119

10

0.0154

12

0.242

8.5

IL LOESS-SL LOESS

0.105

1

0.111

4

0.132

16.5

0.0193

15

0.267

10

IG LOESS-LFILTERW3

0.158

19.5

0.136

11

0.092

1.5

0.0231

20

0.242

8.5

IG LOESS-SL FILTERW7

0.113

3.5

0.111

4

0.119

10

0.0154

12

0.217

4

IST SPLINE-SL LOESS

0.121

6

0.102

1

0.119

10

0.0233

22

0.192

1

IST SPLINE-SL FILTERW3

0.157

18

0.139

12

0.092

1.5

0.0229

17.5

0.209

2.5

IIST SPLINE-SL FILTERW7

0.118

5

0.127

9

0.132

16.5

0.0229

17.5

0.209

2.5

Q SPLINEG

0.158

19.5

0.192

17.5

0.096

3.5

0

2

0.275

12.5

QS PLINER

0.166

22

0.123

8

0.096

3.5

0

2

0.275

12.5

Q SPLINEG-SL LOESS

0.138

11

0.198

19

0.119

10

0.00769

7.5

0.225

6

Q SPLINEG-SL FILTERW3

0.144

12.5

0.186

15.5

0.172

23

0.00758

5

0.317

16

Q SPLINEG-SL FILTERW7

0.149

14

0.192

17.5

0.106

6

0.00758

5

0.225

6

QS PLINER-SL LOESS

0.155

16

0.105

2

0.105

5

0.00769

7.5

0.225

6

QS PLINER-SL FILTERW3

0.155

16

0.111

4

0.145

21

0.00758

5

0.325

17.5

QS PLINER-SL FILTERW7

0.169

23

0.117

6.5

0.119

10

0.0114

9

0.275

12.5

Table 6

IMPROVEMENT of location normalization methods. IMPROVEMENT is defined (in the Results) based on improvement of LOOCV classification error rate of a given normalization method over that of N ONRM. The methods are arranged in the same order as those in Table 5. For a given data set, the biggest IMPROVEMENT(s) is shown in bold. The methods and data sets are described in Tables 1, 2 and 4, respectively.

Location Normalization method

IMPROVEMENT (%, LIVER CANCER)

IMPROVEMENT (%, LYMPHOMA)

IMPROVEMENT (%, RENAL CELL CARCINOMA)

IMPROVEMENT (%, GASTRIC CARCINOMA)

IMPROVEMENT (%, LUNG CANCER)

IMPROVEMENT RANGE (%)

N ONRM

0

0

0

0

0

0 - 0

GMEDIAN

19

7

33

22

5

5 – 33

SL LOESS

33

-2

44

56

3

-2 – 56

SL FILTERW3

23

19

44

45

0

0 – 45

SL FILTERW7

29

5

44

34

9

5 – 44

IG LOESS

34

30

44

33

5

5 – 44

IL LOESS

46

42

44

33

23

23 – 46

IST SPLINE

36

33

52

56

7

7 – 56

IG SG LOESS

33

51

44

100

21

21 – 100

IG LOESS-SL LOESS

44

56

50

56

33

33 – 56

IL LOESS-SL LOESS

48

58

44

44

26

26 – 58

IG LOESS-SL FILTERW3

22

49

61

33

33

22 – 61

IG LOESS-SL FILTERW7

44

58

50

56

40

40 – 58

IST SPLINE-SL LOESS

40

62

50

33

47

33 – 62

IST SPLINE-SL FILTERW3

22

48

61

34

42

22 – 61

IIST SPLINE-SL FILTERW7

42

52

44

34

42

34 – 52

Q SPLINEG

22

28

59

100

23

22 – 100

QS PLINER

18

54

59

100

23

18 – 100

Q SPLINEG-SL LOESS

32

26

50

78

37

26 – 78

Q SPLINEG-SL FILTERW3

29

30

27

78

12

12 – 78

Q SPLINEG-SL FILTERW7

26

28

55

78

37

26 – 78

QS PLINER-SL LOESS

23

61

56

78

37

23 – 78

QS PLINER-SL FILTERW3

23

58

39

78

9

9 – 78

QS PLINER-SL FILTERW7

16

56

50

67

23

16 – 67

https://static-content.springer.com/image/art%3A10.1186%2F1471-2105-6-191/MediaObjects/12859_2004_Article_516_Fig4_HTML.jpg
Figure 4

Bar plots of leave-one-out cross-validation error rates for k -NNs in Table 5. The classifiers were estimated from five data sets (Table 4) either without normalization (N ONRM) or normalized using twenty-three normalization techniques that remove spatial- and/or intensity effect to varying degrees (Tables 1 and 2). In each plot, the normalization methods are arranged in the following order: (A) Methods that remove no dye bias (GMEDIAN), or a single dye bias (SL LOESS, SL FILTERW3, SL FILTERW7, IG LOESS, IL LOESS, IST SPLINE). (B) Methods that remove two dye biases (IG SG LOESS, IG LOESS-SL LOESS, IL LOESS-SL LOESS, IG LOESS-SL FILTERW3, IG LOESS-SL FILTERW7, IST SPLINE-SL LOESS, IST SPLINE-SL FILTERW3, IST SPLINE-SL FILTERW7). (C) Qspline-related methods (Q SPLINEG, QS PLINER, Q SPLINEG-SL LOESS, Q SPLINEG-SL FILTERW3, Q SPLINEG-SL FILTERW7, QS PLINER-SL LOESS, QS PLINER-SL FILTERW3, QS PLINER-SL FILTERW7).

https://static-content.springer.com/image/art%3A10.1186%2F1471-2105-6-191/MediaObjects/12859_2004_Article_516_Fig5_HTML.jpg
Figure 5

Rank summary for location normalization methods. The median and upper quantile ranks of each method are defined as the median and upper quantile values of the ranks of each method across all five data sets (see Table 5, "Ranks"). The bar plots present a visual depiction of the results in the table. (Median ranks are shown in pink; upper quantile ranks are shown in blue.)

Single-bias-removal methods

These strategies can be classified into two categories, spatial-dependent and intensity-dependent normalization methods. Three spatial-dependent normalization methods (SL LOESS, SL FILTERW3, SL FILTERW7) reduce k-NN LOOCV classification error rates to a similar extent (Tables 5 and 6) and have almost identical ranks (Figure 5), despite the fact that their abilities to remove spatial effect are quite different (Figure 2). Since both SL LOESS and SL FILTERW7 fail to remove local spatial patterns effectively (Figure 2, rows 2 and 4), SL FILTERW3 may be too aggressive in removing "dye effect" (Figure 2, row 3). However, the three intensity-dependent methods (IG LOESS, IL LOESS, IST SPLINE) reduce k-NN LOOCV classification error rates to different degrees. The k-NN LOOCV classification error rate and rank of IG LOESS are similar to those of the three spatial-dependent methods (SL LOESS, SL FILTERW3, SL FILTERW7) (Figure 5), whereas IL LOESS, which removes intensity effect more completely than IG LOESS, has smaller k-NN LOOCV classification error rates than IG LOESS in all five data sets. IST SPLINE, which uses a rank invariant set for normalization, is also better than IG LOESS in all five data sets (Figure 5).

In all five data sets, except for LYMPHOMA (SL LOESS), the single-bias-removal normalization methods consistently yield smaller LOOCV classification error rates than no-bias-removal methods, N ONRM and GMEDIAN (which only sets the median of the distribution of M values to zero). The greatest benefit, an IMPROVEMENT of 56%, is seen with GASTRIC CARCINOMA (SL LOESS, IST SPLINE) (Table 6).

Double-bias-removal methods

IG SG LOESS removes both spatial- and intensity effect in one step, whereas the remaining seven approaches are two-step strategies consisting of single-bias-removal methods applied sequentially (first a method to remove intensity effect, followed by a method to remove spatial effect).

In general, double-bias-removal methods have smaller k-NN LOOCV classification error rates and bigger IMPROVEMENT than single-bias-removal methods, and all perform better than N ONRM and GMEDIAN (Tables 5 and 6, Figures 4 and 5). Using an arbitrary cut-off value of 10 for both median and upper quantile ranks (Figure 5), IG LOESS-SL FILTERW7, IST SPLINE-SL LOESS and IG LOESS-SL LOESS (all of which remove intensity effect globally and then spatial effect locally) appear to be the best methods overall. These three two-step strategies not only have the lowest ranks amongst all normalization methods and across all data sets (Figure 5), they also showed most consistent and significant IMPROVEMENT over both N ONRM and GMEDIAN across all five data sets (Table 6). The benefits of using IG LOESS-SL FILTERW7 over no normalization (N ONRM) range from an IMPROVEMENT value of 40% in LUNG CANCER to 58% in LYMPHOMA (Table 6), whereas the IMPROVEMENT values of IST SPLINE-SL LOESS range from 33% in GASTRIC CARCINOMA to 62% in LYMPHOMA and the IMPROVEMENT values of IG LOESS-SL LOESS range from 33% in LUNG CANCER to 56% in GASTRIC CARCINOMA.

The ranks of the SL FILTERW3-related approaches (IG LOESS-SL FILTERW3, IST SPLINE-SL FILTERW3, Q SPLINEG-SL FILTERW3, QS PLINER-SL FILTERW3) are higher than their SL FILTERW7 counterparts (Figure 5), suggesting that a window size of 7 × 7 is more preferable than that of 3 × 3. A smaller window size may over normalize the data, and thus conceal real biological variations.

Compared to the two-step approaches, the rank of the one-step method, IG SG LOESS, is higher than IG LOESS-SL FILTERW7 and IST SPLINE-SL LOESS (yet lower than IG LOESS-SL FILTERW3 and IST SPLINE-SL FILTERW3). This indicates that the one-step IG SG LOESS has no apparent advantage over the two-step bias-removal strategies.

Overall, the classification performances of data normalized using the double-bias-removal methods are better than that of N ONRM, and the benefits (IMPROVEMENT) of doing so range from 21% in the case of LUNG CANCER (IG SG LOESS) to 100% in GASTRIC CARCINOMA (IG SG LOESS) (Table 6).

Qspline-related approaches

Unlike the location normalization methods discussed above, qspline-related approaches require a target array. Q SPLINEG and QS PLINER are single-bias-removal techniques and use G and R respectively as the target array. The reduction in k-NN LOOCV classification error rates for these methods is quite significant compared to the other single-bias-removal methods. However, it is noticeable that although Q SPLINEG and QS PLINER produce similar results in almost all data sets, their results are different in LYMPHOMA (Figures 4 and 5). In addition, when Q SPLINEG or QS PLINER is combined with one of the three spatial-dependent methods, the rank of the resulting double-bias-removal technique is different from that of its counterpart technique (Figure 5). These results suggest that, similar to other baseline array-based normalization methods [14], the performances of the qSpline-related methods may also depend on the choice of the target array.

Overall, the classification performance of data normalized using the qspline-related methods is better than N ONRM by IMPROVEMENT values of 9% in LUNG CANCER (QS PLINER-SL FILTERW3) and of 100% in GASTRIC CARCINOMA (Q SPLINEG, QS PLINER). None of these qSpline-related methods, however, outperforms the IG LOESS-SL FILTERW7 (Table 6).

Scale normalization

Figure 6 shows boxplots of the distribution of non-normalized M values for microarrays in the five studies. Scale effect is more apparent between (right) rather than within (left) microarrays in a study. The LYMPHOMA data set shows considerable variations in box size and whisker length both within and between microarrays.
https://static-content.springer.com/image/art%3A10.1186%2F1471-2105-6-191/MediaObjects/12859_2004_Article_516_Fig6_HTML.jpg
Figure 6

Boxplots of the distributions of non-normalized M values for microarrays in the five studies. In each boxplot, the box depicts the main body of the data and the whiskers show extreme values. The variability is indicated by the size of the box and the length of the whiskers (marray/marraymaBoxplot(y="maM")). Each panel in the left-hand column shows results for M values at the local level of a microarray chosen at random from a given data set. The bars are color-coded by PT group. Each panel in the right-hand column shows results for M values at the global level for 50 microarrays chosen at random from a given data set (the total number of microarrays in RENAL CELL CARCINOMA is 38). Each row corresponds to a particular study.

Tables 7 and 8 and Figure 7 show LOOCV classification error rates, ranks and IMPROVEMENT for the k-NN classifiers estimated using 3 scale normalization methods combined with other spatial- and/or intensity-dependent normalization methods (18 strategies in all). For data normalized first with spatial- and/or intensity-dependent methods, little or no reduction in LOOCV classification error rates was observed when within-microarray scale normalization (W SCALE) was applied later. However, when between-microarray scale normalization (B SCALE) was used alone, or when both scale normalization techniques were used sequentially (WB SCALE), there was an increase in both median and upper quantile ranks (Figure 7), suggesting that B SCALE should not be applied on the studied data sets. With regard to our running example, the LYMPHOMA data set, scale normalization has no apparent beneficial effect on classification performance.
Table 7

Leave-one-out cross-validation k-NN error rates for scale normalized data. Error rate and rank of each scale normalization method. "Rank" is described in detail in Table 5. For a given data set, the smallest error rate(s) and rank(s) are shown in bold. The methods and data sets are described in Tables 3 and 4, respectively.

Location, Scale Normalization method

LIVER CANCER

LYMPHOMA

RENAL CELL CARCINOMA

GASTRIC CARCINOMA

LUNG CANCER

 

Error Rate

Rank

Error Rate

Rank

Error Rate

Rank

Error Rate

Rank

Error Rate

Rank

N ONRM

0.202

19.5

0.266

18.5

0.237

24

0.0347

14.5

0.359

19.5

N ONRM, W SCALE

0.185

14.5

0.303

23.5

0.211

22.5

0.0270

12

0.350

17.5

N ONRM, B SCALE

0.227

23.5

0.272

20.5

0.132

8

0.0615

22

0.425

24

N ONRM, WB SCALE

0.227

23.5

0.303

23.5

0.132

8

0.0462

21

0.392

23

SL LOESS

0.136

9

0.272

20.5

0.132

8

0.0154

3

0.350

17.5

SL LOESS, W SCALE

0.127

7

0.266

18.5

0.132

8

0.0193

6

0.342

15.5

SL LOESS, B SCALE

0.202

19.5

0.260

17

0.145

14.5

0.1000

24

0.300

11.5

SL LOESS, WB SCALE

0.191

16

0.284

22

0.119

2

0.0846

23

0.283

9.5

IG LOESS

0.133

8

0.186

15

0.132

8

0.0231

9.5

0.342

15.5

IG LOESS, W SCALE

0.141

10

0.148

11

0.132

8

0.0193

6

0.317

13.5

IG LOESS, B SCALE

0.215

22

0.216

16

0.158

18.5

0.0308

13

0.375

21

IG LOESS, WB SCALE

0.202

19.5

0.179

14

0.158

18.5

0.0231

9.5

0.383

22

IL LOESS

0.110

3.5

0.154

12

0.132

8

0.0231

9.5

0.275

7

IL LOESS, W SCALE

0.116

6

0.161

13

0.145

14.5

0.0231

9.5

0.300

11.5

IL LOESS, B SCALE

0.193

17

0.111

3

0.145

14.5

0.0385

17.5

0.359

19.5

IL LOESS, WB SCALE

0.202

19.5

0.105

1

0.145

14.5

0.0424

20

0.317

13.5

IL LOESS-SL LOESS

0.105

1.5

0.111

3

0.132

8

0.0193

6

0.267

4.5

IL LOESS-SL LOESS, W SCALE

0.105

1.5

0.136

9.5

0.132

8

0.00769

1

0.267

4.5

IL LOESS-SL LOESS, B SCALE

0.160

12

0.130

8

0.211

22.5

0.0385

17.5

0.275

7

IL LOESS-SL LOESS, WB SCALE

0.152

11

0.123

6

0.158

18.5

0.0347

14.5

0.259

3

IG LOESS-SL FILTERW7

0.113

5

0.111

3

0.119

2

0.0154

3

0.217

2

IG LOESS-SL FILTERW7, W SCALE

0.110

3.5

0.124

7

0.119

2

0.0154

3

0.209

1

IG LOESS-SL FILTERW7, B SCALE

0.180

13

0.117

5

0.171

21

0.0385

17.5

0.275

7

IG LOESS-SL FILTERW7, WB SCALE

0.185

14.5

0.136

9.5

0.158

18.5

0.0385

17.5

0.283

9.5

Table 8

IMPROVEMENT of the scale normalization methods. IMPROVEMENT is described in detail in Table 6. For a given data set, the biggest IMPROVEMENT(s) is shown in bold. The methods and data sets are described in Tables 3 and 4, respectively.

Location, Scale Normalization method

IMPROVEMENT (%, LIVER CANCER)

IMPROVEMENT (%, LYMPHOMA)

IMPROVEMENT (%, RENAL CELL CARCINOMA)

IMPROVEMENT (%, GASTRIC CARCINOMA)

IMPROVEMENT (%, LUNG CANCER)

N ONRM

0

0

0

0

0

N ONRM, W SCALE

8

-13

11

22

3

N ONRM, B SCALE

-12

-2

44

-77

-18

N ONRM, WB SCALE

-12

-13

44

-33

-9

SL LOESS

33

-2

44

56

3

SL LOESS, W SCALE

37

0

44

44

5

SL LOESS, B SCALE

0

2

39

-188

16

SL LOESS, WB SCALE

5

-7

50

-144

21

IG LOESS

34

30

44

33

5

IG LOESS, W SCALE

30

44

44

44

12

IG LOESS, B SCALE

-6

19

33

11

-4

IG LOESS, WB SCALE

0

33

33

33

-7

IL LOESS

45

42

44

33

23

IL LOESS, W SCALE

43

39

39

33

16

IL LOESS, B SCALE

4

58

39

-11

0

IL LOESS, WB SCALE

0

61

39

-22

12

IL LOESS-SL LOESS

48

58

44

44

26

IL LOESS-SL LOESS, W SCALE

48

49

44

78

26

IL LOESS-SL LOESS, B SCALE

21

51

11

-11

23

IL LOESS-SL LOESS, WB SCALE

25

54

33

0

28

IG LOESS-SL FILTERW7

44

58

50

56

40

IG LOESS-SL FILTERW7, W SCALE

46

53

50

56

42

IG LOESS-SL FILTERW7, B SCALE

11

56

28

-11

23

IG LOESS-SL FILTERW7, WB SCALE

8

49

33

-11

21

https://static-content.springer.com/image/art%3A10.1186%2F1471-2105-6-191/MediaObjects/12859_2004_Article_516_Fig7_HTML.jpg
Figure 7

Rank summary for scale normalization methods. The median ranks and upper quantile ranks are defined as described in Figure 5. The bar plots present a visual depiction of the results in the table. (Mean ranks are shown in pink; median ranks are shown in blue.) In each plot, normalization strategies are arranged in the following order: a location normalization method, a location normalization method followed by W SCALE (+W SCALE), a location normalization method followed by B SCALE (+B SCALE), a location normalization method followed by WB SCALE (+WB SCALE).

Discussion

This computational investigation employed two types of visual diagnostic plots and k-NN LOOCV classification error rates to evaluate a broad suite of known normalization strategies. These analyses were applied to cDNA microarray data from five published cancer studies. Since all these data sets were acquired using GenePix image analysis software and a recent study showed that background adjustment using GenePix can increase variability of microarray data and compromise downstream data analyses [3], we used foreground intensity values of the probes without background adjustment in this work. The normalization approaches examined are based on a variety of different techniques and implementations that are readily available and accessible.

Our results show that the LOOCV classification error of k-NN classifiers depends on how much of spatial- and intensity effect can be removed by a normalization strategy. Overall, the single-bias-removal location approaches perform better than GMEDIAN and N ONRM, while the double-bias-removal location strategies perform better than the single-bias-removal location approaches. Of the twenty-three location normalization techniques investigated, three two-step processes (IG LOESS-SL FILTERW7, IST SPLINE-SL LOESS and IG LOESS-SL LOESS), all of which removes intensity effect at the global level and spatial effect at the local level, appear to be the most effective at reducing LOOCV classification error. However, removing spatial- or intensity effect alone is not sufficient for reducing LOOCV classification error (see below).

A recent review of normalization methods [26] raised the concern that removing spatial effect (SL LOESS and the related methods) may add additional noise to normalized data, and suggested that a safe alternative was removing only intensity effect at the local level (IL LOESS) [26]. Our results show that, although the classification performance of data normalized with SL LOESS alone can be worse than non-normalized data as in the case of the LYMPHOMA data set, when SL LOESS is combined with another intensity-dependent approach (IG LOESS, IL LOESS, IST SPLINE, Q SPLINEG, or QS PLINER), there is considerable improvement over N ONRM, with IMPROVEMENT ranging from 23% in LIVER CANCER (QS PLINER-SL LOESS) to 78% in GASTRIC CARCINOMA (QS PLINER-SL LOESS, Q SPLINEG-SL LOESS). Thus, removing both spatial- and intensity effect is beneficial for the downstream analytical task of classification. Another study compared various lowess-based single-bias-removal intensity normalization approaches, and found that IL LOESS may not significantly improve the results compared to IG LOESS [27]. Our results show that the benefits (IMPROVEMENT) of IG LOESS over N ONRM range from 5% in LUNG CANCER to 44% in RENAL CELL CARCINOMA; while that the benefits (IMPROVEMENT) of IL LOESS over N ONRM range from 23% in RENAL CELL CARCINOMA to 46% in LIVER CANCER. Therefore, IL LOESS performs better than IG LOESS in our study. However, as a single-bias-removal approach, IL LOESS still fail to outperform IG LOESS-SL FILTERW7, IST SPLINE-SL LOESS and IG LOESS-SL LOESS, which are the best overall methods and whose IMPROVEMENT values over N ONRM range from 40% in LUNG CANCER to 58% in LYMPHOMA for IG LOESS-SL FILTERW7, from 33% in GASTRIC CARCINOMA to 62% in LYMPHOMA for IST SPLINE-SL LOESS and from 33% in LUNG CANCER to 56% in GASTRIC CARCINOMA for IG LOESS-SL LOESS (Table 6).

A previous study employed k-NN classification of diluted samples to assess a small number of global linear methods for normalization [28]. The study presented here is more comprehensive, both in terms of the range of data sets and the diversity of normalization techniques. Our results indicate that the k-NN LOOCV classification error of real biological samples provides an informative functional quantitative measure that can be used to evaluate normalization approaches.

Differences in scale between microarrays can arise from both unwanted technical factors (differences in experimental reagents, equipment, personnel, and so on), as well as from genuine biological variations. The scale normalization techniques applied here aim to remove unwanted technical factors, and assume the existence of little biological variations between samples. For the five studied data sets, scale normalization of non- or location-normalized data do not result in an overall reduction in LOOCV classification error. Indeed, two between-microarray normalization methods (B SCALE, WB SCALE) result in an overall increase in LOOCV classification error (poorer performance, Figure 7). These results suggest that in the examined cancer-related data sets, there can be considerable genuine biological variations (which is plausible because genomic aberrations found in cancer cells [29, 30] may alter the number and nature of expressed genes compared to normal cells), and that these variations are masked by the applied scale normalization. The data sets considered here do not contain replicated data, so it is difficult to ascertain how much of the scale effect result from unwanted technical factors. Scale normalization may be warranted in situations where technical differences can be discerned by examination of the replicated data and genuine biological variations are known or believed to exist. In such cases, scale normalization using external control samples may be more useful than the total gene approaches.

While our empirical analyses are thoroughgoing in terms of both normalization procedures and test data sets, we acknowledge that there are two caveats in this study that deserve attention and further investigation. First, we employed the LOOCV classification error as a functional measure to assess normalization methods. In principle, LOOCV provides an almost unbiased estimate of the generalization ability of a classifier [31], especially when the number of the available training samples is severely limited (as in the case of LYMPHOMA and RENAL CELL CARCINOMA in Table 4), and is thus highly desirable for model selection or other relevant algorithm evaluation [32, 33]. However, it is also known that the LOOCV error estimator may have high variance in some situations [34, 35], which could in turn affect the accuracy of the rankings of the normalization methods. Empirically, however, we found that the LOOCV errors we obtained from various round of classification are quite stable, therefore we believe that our estimation is in practice reliable and suitable for ranking. Nevertheless, error estimators that have shown to have low variance (e.g., bootstrapping and k-fold cross-validation [34, 35]) are worth further investigation in the future.

The second caveat of this work is that normalization methods were evaluated using k-NN classification without the aid of auxiliary techniques, such as feature selection. The reasons we did not employ feature selection, but rather used all the probes that are present in the majority of the microarrays for classification are as follow: i) We believe that the influence of the dye effect (which usually affect a large number of the probes) on the downstream data analysis can be better and more consistently reflected when a large number of the probes are examined. As such, using all valid probes for training a classifier can best reflect the effectiveness of the normalization methods, whereas using subsets of the probes may generate inconsistent results due to the heterogeneous nature of the dye effect across microarrays. ii) We also included low intensity probes in the analyses. Although this may add noise and therefore could compromise the absolute classification performance of the examined normalization methods, we nevertheless think that these probes should not be excluded because reducing variability in low intensity probes is by itself an important objective of normalization methods. That is, a good normalization approach should be able to reduce variability in both low intensity- and high intensity probes effectively. And iii) we are aware that k-NNs without feature selection may add variability to the classification results, however, k-NN classification is also appealing in that it is simple and requires no data pre-processing or assumption on data distribution. In addition, k-NN classifiers have been widely used in many classification tasks including high-dimensional problems arising from image and text data [36].

Due to the above two caveats, the relative rankings of the investigated normalization strategies can hardly be obtained accurately in this work. For example, our results show that IG LOESS-SL FILTERW7, IST SPLINE-SL LOESS and IG LOESS-SL LOESS reduce LOOCV classification errors most consistently and effectively across all five data sets. It is difficult, however, to determine further which of these three strategies is the best, because small differences in classification results can either arise from inherent differences in these approaches and/or from the variability introduced by the LOOCV error estimator and less optimal k-NN classifiers. Moreover, our results should not be taken as a warrant of directly using baseline methods, such as k-NNs without feature selection, for high-dimensional classification tasks. More investigations are needed to understand the interplay between normalization (which improves data quality) and feature selection (which improves the classifier by throwing away non-informative data) to ascertain normalization strategies to produce an optimal classifier.

Conclusion

Using LOOCV error of k-NNs as the evaluation criterion, we assessed a variety of normalization methods that remove spatial effect, intensity effect and scale differences from cDNA microarray data. Overall, the single-bias-removal location approaches (which remove either spatial- or intensity effect from the data) perform better than GMEDIAN and N ONRM, while the double-bias-removal location strategies (which remove both spatial- and intensity effect) perform better than the single-bias-removal location approaches. Of the 41 different strategies examined, IG LOESS-SL FILTERW7, IST SPLINE-SL LOESS and IG LOESS-SL B SCALE, all of which are two-step approaches and remove both intensity effect at the global level and spatial effect at the local level, appear to be the most effective at reducing LOOCV classification error. The investigated scale normalization methods do not have beneficial effect on classification performance. These results also indicate that spatial- and intensity effect do have profound impact on downstream data analyses, such as classification, and that removing these effects can improve the quality of such analyses.

Methods

Extant data sets and software

Table 4 summarizes relevant information on the cDNA microarray data sets from the Stanford Microarray Database (SMD) reexamined here. These data sets were selected because the published studies assayed samples from distinct cancers, the profiling experiments were performed at different times, four out of the five data sets were produced by different investigators, and the microarrays used were printed with different probes on different occasions. The LYMPHOMA study has been used as the illustrative, running example.

A variety of computational tools for manipulating, analyzing, and visualizing microarray data are available. These include open source implementations based on the R language for statistical computing http://​www.​r-project.​org[37] such as the Bioconductor http://​www.​bioconductor.​org, MAANOVA http://​www.​jax.​org/​staff/​churchill/​labsite/​software/​download.​html, tRMA http://​www.​pi.​csiro.​au/​gena/​tRMA, and braju http://​www.​maths.​lth.​se/​help/​R/​aroma packages. Standard R and Bioconductor packages and functions were used apart from one normalization method found in MAANOVA (joint removal of both spatial- and intensity effect at the global microarray level, IG SGB SCALE) and two normalization methods found in tRMA (removal of spatial effect at the local PT level, SL FILTERW3 and SL FILTERW7).

Pre-normalization data processing

For each spot, the foreground red (R f ) and green (G f ) quantitated fluorescent intensities (acquired using GenePix image analysis software) of the arrayed DNA sequences were used to compute the non-normalized log ratio, M = log2(R f / G f ), and average log intensity, https://static-content.springer.com/image/art%3A10.1186%2F1471-2105-6-191/MediaObjects/12859_2004_Article_516_IEq6_HTML.gif . Because of the concern that local background values estimated by GenePix may add additional noise to the data [3], these values were not subtracted from their corresponding foreground values. For a given microarray, the log ratios were normalized using location- and/or scale-normalization techniques and its particular configuration (the LYMPHOMA and GASTRIC CARCINOMA studies employed microarrays with two and three distinct configurations respectively).

Normalization methods

Tables 1 and 2 summarize the 23 location normalization methods that remove none, one, or both of spatial- and intensity effect (detailed descriptions of how they adjust M values can be found elsewhere [4, 6, 12, 13, 17, 21, 38, 39]). In particular, Table 1 includes two methods that remove no spatial- or intensity-dependent dye bias: (i) N ONRM neither removes any effect nor alters the distribution of M values; and (ii) GMEDIAN does not remove any effect but acts as a baseline normalization method because it sets the mean or median of M to zero. There are eight methods that remove either spatial- or intensity effect: (i) SL B SCALE removes spatial effect at the PT level using lowess; (ii) SL FILTERW3 and SL FILTERW7 remove spatial effect using median filters of the block sizes 3 × 3 and 7 × 7, respectively [17]; (iii) IG B SCALE removes intensity effect at the global level; (iv) IL B SCALE removes intensity effect at the local level and as a byproduct removes spatial effect partially; (v) IST SPLINE removes intensity effect at the global level using rank invariant set and a spline smoothing technique [38]; and (vi) QS PLINER (Q SPLINEG) removes intensity effect at the global level using spline smoothing applied to quantiles obtained from R (G) and using the geometric mean of the R (G) channels of all arrays as the target array [13]. In Table 2, IG SG LOESS is a one-step process that removes global intensity effect and global spatial effect, while the remaining thirteen strategies are two-step processes that remove both dye effect by combining methods in Table 1.

Table 3 summarizes the three scale normalization methods used (detailed descriptions of how these methods adjust the scale of M values can be found elsewhere [4]). W SCALE adjusts the scale of M values at the PT level. B SCALE adjusts the scale of M values globally across all microarrays in a data set. WB SCALE adjusts the scale locally followed by globally, in two steps. These scale normalization methods were applied to non-normalized data (N ONRM) and to data that had been normalized using the five location methods SL LOESS, IG LOESS, IL LOESS, IL LOESS-SL LOESS, or IG LOESS-SL FILTERW7. These methods were selected to represent methods that remove spatial and/or intensity effect at different levels.

Post-normalization data processing

For the five cancer-biology studies, examination of the published data indicated that probes printed on different microarrays (even those with the same configuration) were not necessarily identical. For the N microarrays associated with a given study (N can be equated with the value given for "Microarrays" in Table 4), the 41 data sets used to estimate k-NN classifiers and to determine their LOOCV classification errors were created as follows. Each microarray was handled as described in "Pre-normalization data processing" and the ensuing M values were normalized using the 41 distinct location and/or scale techniques discussed above. A probe was retained for further processing only if it was printed and present (i.e., successfully measured and computed) in 95% of the N microarrays. If a probe met these criteria, missing M values were imputed using the k-NNimpute algorithm [40] as implemented in the Bioconductor package/function pamr/pamr.knnimpute(k = 10) [41]. Given the 41 data sets, the M values for a probe in all N microarrays were centered and rescaled to a unit norm. For LYMPHOMA, the final dimensionality (number of probes after post-normalization data processing) of each of the N = 81 data points was 6,850 ("Probes"). The 41 post-normalized data sets for the five examined studies are available at http://​paccm.​upmc.​edu/​BMCsup.​html.

Classification error

Given D data points, each of which is assigned to one of K categories (e.g., "normal", "DLBCL", "FL"), a LOOCV procedure for this K-class data set is as follows. The data set is partitioned into a test set of one data point and a learning set of D-1 data points. The learning set is used to train a classifier and the ensuing model is employed to predict the class label of the test data point. This process is repeated so that the class of each data point is predicted using a classifier estimated from all other data points in the data set. Classification error is the number of the instances in which the predicted class of a data point differs from its known class. The error rate is this value divided by the number of data points, D.

k-NN classifier

Given a K-class data set, the k-NN algorithm predicts the class label of a test data point by first finding which of the data points in the data set are its k closest neighbors. The classes of these k nearest neighbors are examined and the class of the test data point decided by a majority vote, with ties being broken at random. If there are ties for the k th nearest data point, all candidates are included in the vote. Classification using k-NNs does not require any special handling of multi-class data sets. A widely employed measure of the proximity of two data points and the one utilized here is the standardized Euclidean distance [42, 43]. Since all probes are treated with equal weight, the classification results are affected by all the probes rather than just a subset, as would have been the case if feature selection had been employed. Euclidean distance has been shown to be effective and accurate on a variety of data sets [43, 44].

The optimal number of nearest neighbors, k*, was determined via leave-one-out cross-validation. An original data set of D data points was partitioned into a test set of one data point and a learning set of D - 1 data points. Given a specific k, the k-NN algorithm was used to predict the class of each data point in the learning set using the D - 2 remaining data points. The classification error, ε k , of the learning set was determined. This procedure was performed using k = {3,...,10} and k* taken to be the k producing the smallest classification error, i.e., min k (ε k ). The class of the test data point for the original data set was predicted using k* and the k-NN algorithm. This entire process was repeated such that each of the data points in the original data set was used as a test set. The classification error of the original data was calculated. The k-NN step was performed using the R class/package [45]class/knn.cv(k = "number of neighbors") where "number of neighbors" was set to 3,...,10. The prediction step was performed using class/knn(k = "optimal k") where "optimal k" was k*.

List of abbreviations

AC: 

adenocarcinoma

CCC: 

clear cell carcinoma

DLBCL: 

diffuse large B-cell lymphoma

FL: 

follicular lymphoma

GCC: 

granular cell carcinoma

k-NN: 

k-nearest neighbor

LCLC: 

large cell lung cancer

LOOCV

Leave-one-out cross-validation

lowess

local regression estimation

PC: 

papillary carcinoma

PT: 

print-tip group

SCC: 

squamous cell carcinoma

SCLC: 

small cell lung cancer

SMD: 

Stanford Microarray Database.

Declarations

Acknowledgements

We thank three reviewers for their critical yet helpful comments. We thank Professor David Banks in the Institute of Statistics & Decision Sciences of Duke University for helpful discussion and suggestions. We also thank Aylin Rizki and Paraic A. Kenny for critical reading of the manuscript, and Kevin Peet and Penelope Siig for proofreading the manuscript. This work was supported by the Department of Energy (OBER DEAC0376SF00098), by NIH (grant CA64786 8744), and by an Innovator Award from the Department of Defense (DAMD17-02-1-0438) to M.J.B. Work by I.S.M. was supported by the California Breast Cancer Research Program, National Institute on Aging, National Institute of Environmental Health Sciences, and U.S. Department of Energy under contract No. DEAC0376SF00098.

Authors’ Affiliations

(1)
Life Sciences Division, Lawrence Berkeley National Laboratory
(2)
Dorothy P. and Richard P. Simmons Center for Interstitial Lung Disease, Division of Pulmonary, Allergy and Critical Care Medicine, University of Pittsburgh Medical Center
(3)
Center for Automated Learning and Discovery and Language Technology Institute, School of Computer Science, Carnegie Mellon University

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Copyright

© Wu et al; licensee BioMed Central Ltd. 2005

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://​creativecommons.​org/​licenses/​by/​2.​0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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