 Methodology article
 Open Access
 Published:
Spectral estimation in unevenly sampled space of periodically expressed microarray time series data
BMC Bioinformatics volume 8, Article number: 137 (2007)
Abstract
Background
Periodogram analysis of timeseries is widespread in biology. A new challenge for analyzing the microarray time series data is to identify genes that are periodically expressed. Such challenge occurs due to the fact that the observed time series usually exhibit nonidealities, such as noise, short length, and unevenly sampled time points. Most methods used in the literature operate on evenly sampled time series and are not suitable for unevenly sampled time series.
Results
For evenly sampled data, methods based on the classical Fourier periodogram are often used to detect periodically expressed gene. Recently, the LombScargle algorithm has been applied to unevenly sampled gene expression data for spectral estimation. However, since the LombScargle method assumes that there is a single stationary sinusoid wave with infinite support, it introduces spurious periodic components in the periodogram for data with a finite length. In this paper, we propose a new spectral estimation algorithm for unevenly sampled gene expression data. The new method is based on signal reconstruction in a shiftinvariant signal space, where a direct spectral estimation procedure is developed using the Bspline basis. Experiments on simulated noisy gene expression profiles show that our algorithm is superior to the LombScargle algorithm and the classical Fourier periodogram based method in detecting periodically expressed genes. We have applied our algorithm to the Plasmodium falciparum and Yeast gene expression data and the results show that the algorithm is able to detect biologically meaningful periodically expressed genes.
Conclusion
We have proposed an effective method for identifying periodic genes in unevenly sampled space of microarray time series gene expression data. The method can also be used as an effective tool for gene expression time series interpolation or resampling.
Background
Periodic phenomena are widely studied in biology and there are numerous biological applications where periodicities must be detected from experimental biological data. Because the measured data are often nonideal, efficient algorithms are needed to extract as much information as possible. Spectral estimation has been a classical research topic in digital signal processing and has recently found important applications in DNA microarray time series data analysis. Many spectral estimation methods have been proposed in the past decades, including the modified periodogram, the autoregressive (AR) model, the MUSIC algorithm and the multitaper method [1, 2]. Although all these algorithms have their own advantages, they were all developed based on a basic assumption: the input signal is evenly sampled. However, in many realworld applications, the data can be unevenly sampled. For example, in DNA microarray gene expression experiments, a time series may be obtained with different sampling intervals [3–5]. Furthermore, an evenly sampled time series may contain missing values due to corruption or absence of some expression measurements [6, 7]. A time series with missing values can be considered as an unevenly sampled time series in general.
Recently, several methods for detecting periodic gene expression have been proposed [8–15]. Lu et al. [8] have proposed a periodicnormal mixture (PNM) model to fit transcription profiles of periodically expressed genes in cell cycle microarray experiments. Ahdesmäki et al. [9] proposed a generalpurpose robust testing procedure for finding periodic sequences in multiple time series data, which is based on a robust spectral estimator that is incorporated into a hypothesis testing framework using the socalled Gstatistic together with correction for multiple testing. Chen [10] proposed a statistical inference approach, the C&G procedure, to effectively detect statistically significant periodically expressed genes based on two statistical hypothesis testing procedures. Wichert et al. [11] proposed to use the average periodogram as an exploratory tool to detect the presence of possible periodic genes and give an exact statistical test to determine whether or not a sinusoid is presence. Luan and Li [12] proposed to use the shapeinvariant model combined with a cubic Bspline estimation to model periodic gene expression profiles. Ruf [13] is one of the first to treat evenly sampled gene expression time series with missing values as unevenly sampled data for spectral analysis using the LombScargle periodogram. Bohn et al. [14] have used the LombScargle periodogram in their attempt to detect rhythmic components in the circadian cycle of the Crassulacean acid metabolism plants. Glynn et al. [15] also used the LombScargle periodogram to detect periodic patterns in unevenly spaced gene expression time series. The LombScargle periodogram produces better results on unevenly sampled data than the classical Fourier transform method since it weights the data on a "per point" basis instead of on a "per time interval" basis [16]. Lomb [17] proved that this periodogram is the same as the classical periodogram in the case of equally spaced data. However, since the LombScargle method assumes that there is a single stationary sinusoid wave with infinite support, it introduces spurious periodic components in the periodogram for data with a finite length. Also, due to the effect of noise in the data, it may produce inaccurate estimation results.
In this paper, we propose a new spectral estimation technique for unevenly sampled data. Our method models the signal in a shiftinvariant signal space, for which many theories and algorithms are available [18–25]. In our method, a direct spectral estimation formula is derived based on the Bspline basis that has finite support. Experiments on simulated noisy periodic signals show that our algorithm is more accurate in detecting periodicity compared to the LombScargle algorithm.
Results and discussion
Our method is based on signal reconstruction in a shiftinvariant signal space, where a direct spectral estimation procedure is developed using the Bspline basis. The details of the reconstruction algorithm and the power spectrum density (PSD) estimation are given in the Method Section.
Simulated data
We first test our spectral estimation algorithm on simulated signals to compare the estimation accuracy with the LombScargle method. A cosine curve has been used to represent the ideal expression of a gene that goes from an "on" state, to an "off" state, and then back to "on" [11]. For a gene g and expression level observed at time t_{ i }, we denote the time series by Y_{ g }(t_{ i }),
where ${Y}_{g}({t}_{i})\beta \mathrm{cos}\phantom{\rule{0.2em}{0ex}}(\frac{{\text{t}}_{\text{i}}\pi}{12})+{\epsilon}_{\text{g}}({t}_{i})$
for i = 1,...,N and g = 1,...,G. Our test data consists of simulated time series data for the expression of G = 1000 genes, where 900 of them are random genes (i.e., β = 0) and 100 are noisy periodic genes.
To obtain this dataset, the time series (genes) is first evenly sampled at 48 points. That is, t_{ i }= i, (i = 1,...,48). Then, time points are randomly deleted from each time series to simulate the uneven sampling situation.
Figure 1(a) shows a simulated expression of a gene that has a 24hour period with data samples taken every halfhour. Its corresponding periodogram (see Figure 1(b)) shows a peak at the frequency of 1/24 Hz. Figure 1(c) shows the same cosine signal, but it is now corrupted with Gaussian noise and unevenly sampled. The periodograms, obtained using the LombScargle method and our algorithm, are shown in Figure 1(d). The peak frequencies in the periodograms obtained using the LombScargle method and our method are 1/22 Hz and 1/24 Hz, respectively. Clearly our method is more accurate than the LombScargle algorithm. Our method also produces fewer and smaller false peaks in the spectrum.
In the second simulation test, we use the 100 simulated noisy periodic gene profiles and compare our method with the LombScargle approach in terms of errors in the dominant frequency. In Figure 2, we show the meansquare error in dominant frequency under various percentages of presence entries. From Figure 2, we observe that our method is better than the LombScargle method.
Finally, we use the entire 1000 simulated genes and the false discovery rate (FDR) gene selection strategy using Gstatistic to test the accuracy and sensitivity of our method. LombScargle's test is used for LombScargle method. We added artificial Gaussian noise with mean μ = 0 and various SD values (σ = 0.01, 0.2 and 0.6). In Table 1, we compare the effectiveness of the two methods in detecting periodic gene expressions with different missing ratios and various noise levels under the same False Discovery Rate q. From Table 1, we find that our method is better than the LombScargle method in detecting periodic expressions with various missing ratios. Our method is also more robust than the LombScargle method under different noise levels.
Experimental data
Plasmodium falciparum
We have tested our algorithm on the gene expression data of Plasmodium falciparum, which is one of the species that cause human malaria [27]. The gene expression time series from the asexual intraerythrocytic developmental cycle (IDC) of Plasmodium falciparum are strongly periodic. Identifying periodically expressed genes is useful for understanding the genome of Plasmodium falciparum and designing effective vaccines for prevention of human malaria. In the gene expression database from Bozdech et al. [27], data values at the 23rd and the 29th hours are completely missing. An example of a gene expression profiles from the database is shown in Figure 3(a), and its periodograms obtained by using the LombScargle algorithm and our algorithm are shown in Figure 3(c). The frequencies corresponding to the peaks in the periodograms obtained by using the LombScargle method and our method are 1/43.10 Hz and 1/44.13 Hz, respectively. Another example is shown in Figure 3(b). The frequencies corresponding to the peaks in the periodograms obtained by using the LombScargle method and our method are 1/48.68 Hz and 1/47.85 Hz, respectively (see Figure 3(d)). We can see from these diagrams that our algorithm can effectively reduce the spurious oscillation components in the spectra.
The Plasmodium falciparum dataset was analyzed by Bozdech et al. [27] using the fast Fourier transform (FFT), and later by Glynn et al. [15] using the LombScargle algorithm. Bozdech et al. [27] identified 3719 periodic genes in the Quality Control dataset of Plasmodium falciparum, while Glynn et al. [15] found 4355 periodic genes in the complete dataset of 6875 (excluding those profile with unknown oligo ID). Our analysis has shown that the number of periodic profiles in the complete dataset should be around 3700 to 4000. Our estimate is based on analyzing the trend of the sorted Gstatistic (computed using Equation (14) in Method) as shown in Figure 4(a). The intersection of the two distinct slopes points indicates a sudden change in the Gstatistic trend. Nevertheless, no distinct cutoff between periodic/aperiodic profiles can be identified here. Figure 4(b) shows the histogram plot of the Gstatistic. Note that a profile with larger Gstatistic value implies it is much more likely to be periodic. We see that many of the profiles are likely to be periodic. No distinct valley can be observed in the histogram, indicating that a cutoff for periodicity/aperiodicity is difficult to be obtained here. We also examine the periods of the profiles, and Figure 5 shows the histogram plot. It can be seen that there is a prominent period of 48 hours with a count of around 5000 profiles. This result agreed largely with that of Bozdech et al. [27] (see their Figure 2 that discusses the P. Falciparum IDC Transcriptome phases with a period of roughly 48 hours) and that of Glynn et al. [15] (see the histogram of period values in their Supplementary). Nevertheless, our result also shows a much less prominent peak at a period of 24 hours with a low count of around 400 profiles. In Figure 6(a), we show the top 9 ranking profiles, they can be seen to be highly periodic. In Figure 6(b)–(d) , we show the profiles that ranked around 2000, 4000, and 5000, respectively. Even at around a ranking of 5000, some profiles (e.g. see profile at rank 4997) can still be judged to be somewhat periodic. We provide a ranked list of the 6875 profiles in Additional File 1.
Yeast
Spectral analysis is useful for the identification of cellcycleregulated genes. Spellman et al. [3] monitored genomewide mRNA levels for 6178 yeast ORFs simultaneously using several different methods of synchronization including an α (alpha)factormediated G1 arrest which covers approximately two cellcycle periods with measurements at 7 min intervals for 119 min with a total of 18 time points, a temperaturesensitive cdc15 mutation to induce a reversible Mphase arrest, and a temperaturesensitive cdc28 mutation to arrest cells in G1 phase reversibly, and finally, an elutriation synchronization to produce the elutriation dataset of 14 time points (raw data available at [35]). For the cdc15 experiment, gene expression data were measured every 10 min for 290 min, lacking observations for the 20, 40, 60, 260 and 280 min time points, and gives a total of 24 time points. For the cdc28 experiment, samples were taken every 10 min from 0 to 160 min for a total of 17 time points. These four microarray datasets have spawned a large body of work on the gene expressions of the yeast cell cycle.
Spellman [3] originally identified a total of 800 cellcycle genes in all four datasets, while Wichert et al. [11] claimed 468 cyclic genes in alpha, 766 cyclic genes in cdc15, 105 in cdc28, and 193 in elutriation by using Gstatistic as the test statistic. Chen [10] detected 473 cyclic genes in alpha, 788 cyclic genes in cdc15, 27 in cdc28, and 769 in elutriation by using the same Gstatistic as the test statistic under the same FDR threshold level. However, we found that the fisher pvalue (from Equation (13)) computed using the Gstatistic has weak statistical power with such a short signal length. Instead, we analyze the four yeast datasets for periodicity and rank the gene expression profiles according to their Gstatistic. Figure 7(a)–(d) show the histogram distributions of Gstatistic values for the four datasets. We see that there is a continuum of distribution and a clear cutoff for periodicity/aperiodicity cannot be identified (no obvious valleys exist). The sorted Gstatistic plots in Figure 8(a)–(d) also supported such an observation. Hence, a ranking of the gene expression profiles would be much more informative than just giving an adhoc estimate of the number of periodic genes (see Additional File 2 for a ranked list of all genes in each experiment).
Figure 9(a)–(d) show the 9 top ranking genes in each of the four datasets. In Figure 9(a), we see that six of the nine highestranking expression profiles actually have missing values. Nevertheless, our algorithm was able to restore the missing values and rank the profiles properly. The top ranking profiles in the alpha and the cdc28 datasets can be observed to have two periods within the measurement intervals. This agrees well with the known estimated period of 55–77 minutes and 80–100 minutes for the alpha and cdc28 experiments, respectively. The top ranking expression profiles in the cdc15 dataset are much noisier compared to the top ranking profiles in the other three datasets. The profiles indicate a period of around 80–100 minutes, whereas the known estimated period for this dataset is around 60–80 minutes. The elutriation dataset result of (d) strongly indicated that the measurement interval is around one period (in agreement with many studies done on this dataset). For our top 9 ranking elutriation profiles in (d), 4 of them are within the top 9 ranking profiles in Wichert et al. [11] (see their Figure 6) and 1 is within the top 9 ranking profiles of Chen [10] (see their Figure 2).
As pointed out by Lichtenberg et al. [28], there is a remarkably poor agreement between the numbers of periodically expressed genes detected by various computational methods. To enable a more objective comparison between the performances of different algorithms, they proposed three benchmark sets B1, B2, and B3 (see their website [36]). Set B1 contains a total of 113 genes previously identified as periodically expressed in smallscale experiments. Set B2 contains 352 genes whose promoters were bound by at least one of the 9 known cell cycle transcription factors (i.e., Fkh1, Fkh2, Ndd1, Mcm1, Ace2, Mbp1, Swi4, Swi5, Swi6) in two Chromatin IP studies, and therefore many of the genes in this benchmark set should be expected to be cell cycle regulated. Set B3 contains 518 genes annotated in MIPS [37] as "cell cycle and DNA processing". However, since a large number of genes involved in the cell cycle are not subjected to transcriptional regulation (not periodic) and genes found in B1 were explicitly removed, only a small fraction of the genes in B3 are expected to be periodically expressed. They define a good method as one that is able to reproduce precious findings (B1), extract genes whose promoters are associated with known cell cycle transcription factors (B2), or enriched for genes that play a role in the cell cycle (B3).
Figure 10(a)–(e) show the fraction of benchmark sets recovered (i.e., coverage) as a function of gene rank for the four datasets and the combined set (the Gstatistic in the combined set is obtained by taking the maximum of the corresponding Gstatistic values of the 4 datasets). The performance of all datasets is significantly better than random for B1 and B2. For B3, cdc15 and elutriation performances are close to random, whereas cdc28 performance is better than random. The superior performance of the combined dataset indicated that all experiments are valuable in yeast cell cycle study and should be considered together. Not surprisingly, the coverage for B3 is always less than B1 and B2 since only a small fraction of the genes in B3 are expected to be periodically expressed.
A detail investigation of the expression profiles in the benchmark sets shows that the generally low coverage is really due to the absence of periodicity in many of the profiles. In Figure 11(a)–(c) , we plotted the ranking of the genes in the benchmark sets against the overall ranking in the four datasets. We see that a large portion of the profiles in the benchmark sets is ranked very low in the four datasets. A close examination of these profiles confirms that they are nearly random with no observable periodicity. There could be two possible causes for this: (1) a large number of genes involved in the cell cycle are not directly transcriptionregulated and therefore not periodic; (2) the genes are really periodic but experimental artifacts and noise has corrupted their profiles. Hence, for these profiles, it is expected that no algorithms would be able to identify them as periodic based on just a periodicity score.
In [28], the strength of regulation (i.e., highly regulated genes have large standard deviation in their expression profiles) is an important criterion for the detection of periodically expressed genes. Regulation strength was not used as a criterion by our method (as well as the method of [11]) in detecting profile periodicity since the Gstatistic value given by Equation (14) gives a normalized periodic score. Based on the periodicity criterion alone, our method has comparable performance with [28] for the alpha and cdc28 experiments. For the cdc15 experiment, our result is notably inferior (see Figure 12). However, if we look at the cdc15 profiles as shown in Figure 9, we see that even the high ranking profiles are very noisy, and hence the comparison for cdc15 have lower reliability with regard to periodicity behavior. When regulation strength is taken into consideration as well, the results of [28] clearly outperformance our results for the B1 dataset (see dotted curves in left column of Figure 12). This is not surprising since it was pointed out in [28] that the benchmark datasets B1 and B2 are biased towards periodic genes which are strongly regulated. In fact, it was observed in [28] that regulation strength alone outperforms pure periodicity score for the alpha factor experiment on both B1 and B2 datasets. However, for the B3 dataset, taking regulation strength into account actually gives inferior results for all three experiments. As noted by [28], the B3 dataset is likely to be biased toward small amplitude genes. This suggests that regulation strength is only helpful in situations where genes involved in the cell cycle are also significantly regulated. It would not be useful (and can in fact worsen the performance) in situations where genes are highly regulated but are not involved directly in cell cycle process.
The three benchmark datasets are also analyzed in [29]. Both the method of [29] and our method considered only periodicity as the sole criterion. We cited their results in Figure 13. Comparing their results with our results as shown in Figure 10, we see that for the alpha factor experiment, our results is better for B3, comparable with theirs for B2, and inferior for B1. For the cdc15 experiment, our results are better for all three benchmark datasets. For this experiment, it is interesting to note that although our results are notably inferior to that of [28], they are significantly better than that of [29]. For the cdc28 experiment, our results are better for B1, while comparable for B2 and B3. The above comparative study indicates the difficulty in making general performance comparison between different algorithms even with benchmark datasets due to the differences in dataset characteristic.
Conclusion
In this paper, we have proposed a new spectral estimation algorithm based on a signal reconstruction technique in an unevenly sampled space. The advantage of our algorithm over the LombScargle spectral estimation method is that the new algorithm can effectively reduce the effects of noise and spurious oscillation components and therefore improve the estimation accuracy. Experiments on simulated signals and real gene expression data show that our method is effective in identifying periodically expressed genes. Finally, we remark that this paper focuses on the improvement of periodicity estimation accuracy using spectral analysis algorithms. Another important issue is the statistical significance of the periodicity of a time series. Interested readers are referred to Chen [10], Wichert et al. [11] and Glynn et al. [15], who have used hypothesis testing to address this problem.
Methods
Mathematical model
In the following, we first review existing work on signal analysis in the shiftinvariant signal space, and then derive the new spectral estimation algorithm.
Shannon's signal sampling and reconstruction theorem states that:
Theorem: If f ∈ B_{Ω} = {f ∈ L^{2} : supp $\widehat{f}$ ⊂ [A, A]} and 0 < 2TA ≤ 1, then
where supp $\widehat{f}$ = {x : $\widehat{f}$(x) ≠ 0} and $\widehat{f}$ is the Fourier transform of f defined by
Equation (1) shows that the space of a bandlimited signal is identical to the space:
Dowski et al. [30] have introduced a reconstruction formula for unevenly sampled signals that is a special case of Equation (2):
Since the sinc function has an infinite support and slow decay, it is seldom adopted in real applications. Xian et al. [24] found a good decay function that can replace the sinc basis function, but the new function still has an infinite support. To replace the sinc function with a general function ϕ, we first introduce a signal space that is called the shiftinvariant (also called timeinvariant) signal space:
where the coefficients {c_{ i }} are related to the choice of basis function, ϕ.
Signal reconstruction in the shiftinvariant space is an active research area and there are many mathematical theories and algorithms available [18–25]. When the signal f ∈ V(ϕ), we need to reconstruct signal f from sampled value {f(x_{ i })}, where {x_{ i }} is the sampled point set. If {x_{ i }} is an evenly sampled point set, this problem can be regarded as signal reconstruction in an even sampled space. Otherwise, this is a signal reconstruction problem in an uneven sampled space.
In fact, the wellknown autoregressive (AR) model can be regarded as a special case of signal reconstruction in the above signal space. For a given discrete data sequence x[n] for 0 ≤ n ≤ N  1, the sample at time index n is approximated by a linear combination of the previous K samples in the sequence based on the AR prediction model that can be written as,
where $\tilde{x}$[n] and e[n] represent the estimation of x[n] and the corresponding estimation error, respectively. Yeung et al. [31] have presented an application of the AR model to microarray gene expression time series analysis for gene regulation study. Comparing Equation (4) with Equation (5), it is obvious that Equation (5) is a special case of Equation (4).
For signal reconstruction in the shiftinvariant space, we can characterize its energy density spectrum S_{ xx }(ω) according to Equation (4),. If f(x) ∈ V (ϕ), then the energy density spectrum is given by
where ω is the frequency in Hz. In order to avoid introducing spurious periodic components caused by a basis function ϕ with infinite support, for example, the sinc function, we only consider basis functions with compact support.
PSD estimation algorithm
In [26], Grochenig and Schwab introduce the family of Bspline functions as the basis function with compact support. Assume that supp ϕ ⊂[Ω, Ω] and f(x) ∈ V (ϕ) is defined on a finite interval [A_{1}, A_{2}], then f can be determined completely by the coefficients {c_{ k }} for k ∈ (A_{1}  Ω +1, A_{2} + Ω 1) ∩ Z with
In terms of the definition of the power spectrum density (PSD), we can obtain the following estimation function according to Equation (7)
Coefficients {c_{ i }} can be calculated according to following steps using least squares method [26]:

(1)
Given sampling points x_{1},...,x_{ J }∈ [A_{1}, A_{2}] and corresponding discrete function values y = (y_{1},...,y_{ J }). Assume that J ≥ J_{min} = A_{2}  A_{1} + 2Ω  1 and that the truncated matrix T defined below is invertible. Compute matrix: U = (U_{ jk }), T = T_{ kl }), where
$${U}_{jk}=\phi ({x}_{j}k),{T}_{kl}=\sum _{j=1}^{J}\overline{\phi ({x}_{j}k)}\phi ({x}_{j}l),$$j = 1,...,J, k, l = A_{1}  Ω + 1,..., A_{2} + Ω  1.

(2)
Compute c = T^{1}b according to b = $\overline{U}$y, where $\overline{U}$ denotes the complex conjugate transpose of U and T^{1} is the inverse of T.
Remarks:

(1)
The construction of matrix T has the advantage that T is a positive operator on ℓ^{2}(Z).

(2)
In the case of Bspline, matrix T is invertible under the condition that
$${\mathrm{sup}\phantom{\rule{0.2em}{0ex}}}_{j}({x}_{j+1}{x}_{j})\le \frac{({A}_{2}{A}_{1})}{{A}_{2}{A}_{1}+2\Omega 1}<1$$
That is, the SchoenbergWhitney Theorem implies that T is invertible [32].

(3)
Since the numerical solution of (c_{ k }) can be sensitive to particular sets of intersample spacing, we can approximate the inverse of the illconditioned T by its pseudoinverse using singular value decomposition (SVD).
The Bspline of order N can be defined as the convolutions of (N+1) Bsplines of order 0, i.e. $\phi =\stackrel{N+1}{\stackrel{...}{{\chi}_{[\frac{1}{2},\frac{1}{2}]}\ast \cdots \ast {\chi}_{[\frac{1}{2},\frac{1}{2}]}}}$. It is obvious that supp $\phi \subset [{\scriptscriptstyle \frac{N+1}{2}},{\scriptscriptstyle \frac{N+1}{2}}]$ for a Bspline of order N and its Fourier transform can be easily computed as follows:
Substituting it to (8), we obtain an explicit formulation of the PSD estimation as follows:
We have the following observations on our PSD estimation method:

The proposed method does not make any assumption about the number of frequency components in the data, whereas the LombScargle method assumes that there is only a single stationary sinusoid wave with infinite support. In practice, noise in the data can contribute to many frequency components. Thus, our model is more appropriate for realworld noisy data.

Compared with the traditional PSD estimation algorithms, our method can directly compute the PSD for an unevenly sampled signal from Equation (11). The classical Fourier periodogram based method only can deal with evenly sampled data.

The order N of the Bspline basis function ϕ can be chosen adaptively according to Equation (9). From Equation (9), we know that the relationship between the Bspline order N and the minimum number of sampling points J_{min} is given by N ≈ J_{min}  (A_{2}  A_{1}) such that the matrix T is invertible. If we hold the number of sampling point J and the signal support [A_{1}, A_{2}] fixed, then increasing N (which would result in a smoother Bspline with larger support) would ensures a smoother reconstruction. In practice, some oversampling is done for stability of reconstruction, and we increase the oversampling rate (i.e., number of sample time points per time interval) by timescaling the original signal support appropriately to a smaller interval.

From Equation (11), we see that the periodogram decays more rapidly with increasing N, meaning that the reconstructed signal will be smoother with increasing N. This fact can be used for signal denoising.
Detecting periodically expressed genes
The periodogram of the microarray time series from a periodically expressed gene must contain a peak corresponding to its dominant frequency. In [27], Bozdech et al. use the power ratio test to detect the periodic genes of Plasmodium falciparum. Assuming that the frequency value of the main peak in the periodogram is f_{ m }and consider the frequency band [f_{m1}, f_{m+1}] as f_{ m }'s region of influence (ROI). The power ratio S in [27] is defined to be the ratio of the power in f_{ m }'s ROI, power_{ m }, to the total power of the signal, power_{ total }, i.e.,:
If the power ratio calculated is larger than a threshold, the corresponding profile is considered to be periodic. In [27], the threshold for S is heuristically chosen to be 0.7.
In order to be rigorous statistically, Chen [10] and Wichert et al. [11] use the Fisher Gstatistic test to determine whether a peak in the periodogram is significant or not. They corrected for the multiple testing case using the method of False Discovery Rate (FDR) [33], which controls the expected proportion of false positives in the result. The Fisher Gstatistic test [34] can be used to test for the presence of periodic component in random white noise for finite sample signal. The pvalue for the hypothesis testing for periodicity of a signal g of length N_{0}, using Gstatistic as the test statistic, is given by
where g is the sample realization of the Gstatistic value calculated from the Fisher's Gstatistic given by
n = [N_{0}/2], and p is the largest integer less than 1/x. Equation (14) is computed over the set of normalized Fourier frequencies ω = k/N_{0}, where k = 0,1,...,N_{0}/2. Equation (13) gives an exact pvalue that allows one to test whether a gene expression profile behaves like a purely random white noise process or whether the maximum peak in the periodogram is significant. However, for gene expression profiles of short length, i.e., < 40 time points, the pvalue given by Equation (13) has weak statistical power to determine the number of periodic genes [9, 11]. In view of this, we follow [28] and provide instead a ranking of the expression profiles based on the Gstatistic of Equation (14).
LombScargle method
Here, we briefly review the LombScargle periodogram method. For a time series X(t_{ j }), where i = 1,2,...,N_{0} and zero mean, the normalized periodogram as a function of the angular frequency ω is defined as [16]
where τ is defined by the equation
The statistical significance of the periodic components detected in the periodogram can be evaluated using an exponential probability distribution test [16] which we denoted in this work as the LombScargle test.
Authors' contributionsAWCL worked on mathematical modelling, implementation, and microarray datasets analysis. JX worked on signal reconstruction theories and is responsible for the simulated signal experiments. SHW worked on signal reconstruction theories. DS provided biological insight to this project. HY initiated the project and worked on spectral estimation. All authors read and approved the final manuscript.
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Acknowledgements
This work is supported with a grant from the Hong Kong Research Grant Council (project CityU122005) and the Mathematical Tianyuan Foundation of the Chinese National Science Foundation (Grant number 10526036). We would like to thank the anonymous reviewers for their valuable comments.
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Additional File 1: Ranked list of 6875 profiles of the Plasmodium falciparum dataset based on the Gstatistic. A ranked list of the 6875 profiles from the Plasmodium falciparum dataset [27] based on their Gstatistics. The higher the rank, the more periodic is the profile. (XLS 330 KB)
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Liew, A.W., Xian, J., Wu, S. et al. Spectral estimation in unevenly sampled space of periodically expressed microarray time series data. BMC Bioinformatics 8, 137 (2007). https://doi.org/10.1186/147121058137
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Keywords
 Spectral Estimation
 Periodic Gene
 Sample Time Series
 Regulation Strength
 Gene Expression Time Series