 Correspondence
 Open Access
 Published:
A response to Yu et al. "A forwardbackward fragment assembling algorithm for the identification of genomic amplification and deletion breakpoints using highdensity single nucleotide polymorphism (SNP) array", BMC Bioinformatics 2007, 8: 145
BMC Bioinformatics volume 8, Article number: 394 (2007)
Abstract
Background
Yu et al. (BMC Bioinformatics 2007,8: 145+) have recently compared the performance of several methods for the detection of genomic amplification and deletion breakpoints using data from highdensity single nucleotide polymorphism arrays. One of the methods compared is our nonhomogenous Hidden Markov Model approach. Our approach uses Markov Chain Monte Carlo for inference, but Yu et al. ran the sampler for a severely insufficient number of iterations for a Markov Chain Monte Carlobased method. Moreover, they did not use the appropriate reference level for the nonaltered state.
Methods
We rerun the analysis in Yu et al. using appropriate settings for both the Markov Chain Monte Carlo iterations and the reference level. Additionally, to show how easy it is to obtain answers to additional specific questions, we have added a new analysis targeted specifically to the detection of breakpoints.
Results
The reanalysis shows that the performance of our method is comparable to that of the other methods analyzed. In addition, we can provide probabilities of a given spot being a breakpoint, something unique among the methods examined.
Conclusion
Markov Chain Monte Carlo methods require using a sufficient number of iterations before they can be assumed to yield samples from the distribution of interest. Running our method with too small a number of iterations cannot be representative of its performance. Moreover, our analysis shows how our original approach can be easily adapted to answer specific additional questions (e.g., identify edges).
Background
The recent paper by Yu et al. [1] proposes a new method for the analysis (segmentation) of high density single nucleotide polymorphism (SNP) arrays to detect copy number changes (CNAs) in genomic DNA. Their approach has been designed to be highly sensitive for edge detection and is tailored to SNP arrays. In their paper, Yu et al. compare the performance of their approach with that of several alternative methods initially developed for the analysis of arrayCGH (aCGH) data. The methods compared include Circular Binary Segmentation [2], GLAD [3], CGHseg [4] – though not in the original formulation of their authors, as the recommended adaptive penalization of [4] is not used–, and three Hidden Markov Model approaches: a homogenous one [5], the nonhomogeneous one of Marioni et al. [6], and RJaCGH, our own nonhomogeneous HMM using Markov Chain Monte Carlo (MCMC) with Reversible Jump [7].
The different aCGH technologies, from BACbased aCGH to oligonucleotide aCGH (oaCGH), including Affymetrix SNP arrays, differ in several ways, both in terms of coverage, technology, noise per individual element, requirement for reference samples and minimal DNA quality, and LOH information returned (e.g., see [8–13]). Some of these differences might require customized approaches for SNPbased arrays [11, 13].
Thus, our objective here is not to show the optimality of RJaCGH for SNPbased arrays but, rather, to reanalyze the data of Yu et al. [1] using more appropriate parameters for the Markov Chain Monte Carlo in RJaCGH, which yield much improved performance, as well as to show extensions of our model for edge detection, which show the relevance of modelbased methods of direct interpretation that explicitly return probabilities.
Reanalyzing the data
We will reanalyze the data in [1]: in the original comparison RJaCGH was used with a) the incorrect reference for normal samples and b) too few iterations for both the burnin and posterior sampler in the MCMC algorithm.
The data analyzed, in the nonaltered condition, have a mean value of 1.03 and a median of 1.05. RJaCGH, by default, expects that the "normal" values will be centered around 0. This value of 0 is, often, the result of the log2 of a (normalized) ratio of 1. Expecting values of nonaltered regions to be centered around 0 is not unique to RJaCGH; for instance, Fridlyand et al. [5], in p. 138, explain why they expect that the median copy number of the array will typically be normalized to 0. Likewise, Marioni et al. [6] assume a Gaussian for the log2 ratios of each state, which therefore means that regions with unaltered copy number are expected to show values centered around 0. Similarly, Picard et al. [4] indicate (p. 2) "Array CGH data are normalized with a median set to log2(ratio) = 0 for regions of no change (...)". Now, the last three methods, CGHseg [4], aCGH [5], and BioHMM [6], might not be adversely affected, in terms of edge detection, if the normal samples, instead of being centered around 0, are centered around 1 (as in the current data). However, RJaCGH is adversely affected: our algorithm, by default, uses a step where clones are separated into the three groups "gained", "lost", "no change", and information about the expected value of the nonchanged clones is used to separate these three states, and therefore to identify some of the edges. Appropriately using RJaCGH, thus, requires either normalizing the data so that unaltered areas are centered around 0 or, else, explicitly using the "normal.reference" parameter to the RJaCGH function in our code (this parameter might not have been available in the version used in [1], but recentering the data would have had the same effect).
Second, and more importantly, RJaCGH has been run with a burnin run of 50 iterations and results obtained from 450 runs (TOT parameter set to 500). Except for extremely simple Bayesian models, in reallife usage, much longer runs are often necessary (e.g., [14]) both for the burnin period (i.e., to try to ensure that we are sampling from the true posterior) and for the number of MCMC iterations used after the burnin period (i.e., the number of samples used to actually carry out inferences). The number of iterations should be even larger when we are using Reversible Jump and a complex model as HMM [15–17]. It is extremely unlikely that with only 50 burnin iterations our model would be anywhere near convergence, and thus all inferences from these models are suspect.
Parameters for reanalyzing the data
The data and further details on the analysis and simulations were kindly provided by the first author of the paper, Tianwei Yu. We rerun the RJaCGH analysis, using 10000 burnin iterations and 40000 samples for the posterior. Note that, to depart from the original [1] as little as possible, we do not use multiple chains in parallel (which would, however, be the recommended procedure and would also allow to check for convergence [14, 18], as explained in our paper [7]).
As explained above, we set the reference mean to 1 (parameter "normal.reference" in RJaCGH). We could have, instead, centered all data to ensure that the nonaltered regions were centered around 0. To account for different levels of noise in the data (or to modify the tradeoff between false positive and false negative rates) RJaCGH uses only one parameter, "normal.ref.percentile". This parameter might not have been easily available to the authors of [1] and, thus, none of our key criticisms hinge around nonusage of this parameter. "normal.ref.percentile" is used to set the width of the confidence band based on a Normal (Gaussian) distribution: higher values of "normal.ref.percentile" will tend to incorporate more states into the "nonchange" final state. We have varied "normal.ref.percentile" from 0.5 to 0.99 to construct ROC curves as in Figure 3 of [1]. All code for our analysis is available from [19].
Results
Figure 1 shows our reanalysis using RJaCGH. As can be seen from the figure, in virtually all cases the results with appropriate parameters are much better than those shown in Figure 3 of [1] and the results are clearly competitive with those of other methods. For single aberrations and normal size 200–except with CNA size 15– and trisomies and normal size 40 and (second and fourth columns of the figure) RJaCGH is the best performing method as it is the method with values closest to the upper left corner of the figures. Its performance is comparable to that of the best performing methods with a single aberration and normal size 40 (first column). RJaCGH is a bad performer with the mixed scenarios (columns three and six). Finally, the results from trisomies and normal size of 200 are difficult to compare among methods as this is a scenario where all methods perform poorly: overall, RJaCGH is the method that returns values which are closer to the upper left corner of the figures, but the overall Sensitivities are never large whereas some other methods can achieve higher Sensitivities but at the cost of very large False Discovery Rates. In summary, when using appropriate parameters (number of iterations of the sampler and burnin, as well as the correct reference for normal values) RJaCGH is a competitive method for the analysis of these data.
Searching directly for edges
In the reanalysis above, we used RJaCGH in the default way. This means that the inference about the edges is not one where we estimate the probability of a spot being an edge. As RJaCGH is an HMMbased model, its main objective is to try to assign clones to their true (hidden) state; RJaCGH additionally automatically collapses the hidden states to three biologicallymotivated levels: gained/lost/nochange. Thus, to find edges, we first use RJaCGH to infer the status of a clone (gained, lost, no change) and then we identify the edges by looking for two consecutive probes where status changes. There is, however, a simple and direct procedure to obtain the probability of an edge that does not involve the above indirect procedure. Since we can apply the Viterbi algorithm to every MCMC sample [7], for each MCMC sample we can directly obtain the locations where there is an edge: spot i is an edge if its state –as identified by the path from the Viterbi algorithm– is different from that of spot i + 1. This approach has the advantage of returning the probability of an edge in a given spot, directly incorporating averaging over number of hidden states, and not requiring to specify "normal.ref.percentile". The later also illustrates one difference with regards to the previous approach. In the previous approach, the edges are identified from the "collapsed" classification of all hidden states into gained/lost/nochange (and this is why we required the specification of "normal.ref.percentile"). Here, in contrast, we will identify as an edge any change in state, even if the change in state is between hidden states that will eventually be considered a single biological level in the classification (e.g., if the change in state is between two different hidden states that will later be both considered "gain").
We run the analysis again, to replicate Figure 3 in the original [1]. As with this procedure we obtain the probability of an edge, for ROC curve construction we will declare that a spot is an edge if the probability is above a given threshold, and will generate the ROC curves by changing this threshold. We have varied the threshold from 0 to 0.95 in steps of 0.05 (so the ROC curves are based on 20 threshold values). The results are shown in Figure 2. As can be seen, the results are in most cases slightly better than those in Figure 1 and, thus, also sustain the conclusion that RJaCGH is a competitive method for the analysis of these data. To further illustrate this procedure, and to understand some of the results shown in Figure 2, Figure 3 shows six case examples. Panels a) and b) correspond to a situation (single alteration, normal size of 200 and CNA size of 40) which is among the best performing. In both cases, the probability of an edge is maximal exactly at, or very near to, the spot where the actual edge is located, and there is a very clear separation between spots where there is some probability of an edge and the rest of the spots. Panels c) and d) identify an intermediate case (mixed aberration, normal size of 40, CNA size of 20). In panel d), only two true edges are clearly detected (corresponding to a low sensitivity case), whereas in panel c) in addition to the two true edges with high probability, there are many spots with intermediate probability, which leads to an increase in Sensitivity with FDR almost along the diagonal line as we lower the threshold (since most of the spots with intermediate probabilities of being edges are not true edges). Panels e) and f) are example of one of the worst performing scenarios (trisomy, normal size of 40 and CNA size of 20); panel e) is a usual example where there are many changes in state, very few of which occur at the true location and we, thus, have very low Sensitivity and high FDR; in panel f) we still see many changes in state, but many of the true locations can be identified if we are willing to pay the price of a high FDR. Interestingly, and since the algorithm for RJaCGH incorporates the Viterbi algorithm as part of its computations, finding edges in this way only requires a minimal amount of coding (about 35 lines of C code and 30 lines of wrapper R code).
Finally, there is no need to rerun the algorithm to modify the tradeoff between sensitivity and FDR, since this tradeoff can be changed by changing the probability threshold over which we consider a spot to be an edge. This feature provides added flexibility, which allows users to choose the best threshold for any application, or even to use different thresholds for different probes or chromosomes. Moreover, even if the edge is not located precisely, we can obtain evidence suggestive of the area where an edge is located. For instance, in Figure 3, panel f) the exact location of any edge is not well defined, but there are three areas where spots of high edge probability are located, and an additional two with areas of medium edge probability; these types of representations might suggest refining searches in these areas. In contrast, panel e) is indicative of a situation where the algorithm is likely to be performing poorly, thus alerting users that those results should not be trusted.
Discussion
We have shown (Figure 1) that, when used properly (i.e., with realistic number of chains for the MCMC algorithm and with the correct reference for the normal–nochange–probes), RJaCGH can achieve performance onpar with, or better than, other methods in this data set. Moreover, and in contrast to other methods, the model of RJaCGH is sufficiently flexible that we can directly obtain answers to the questions we are interested in, as shown in Figure 2, where we directly obtain the probabilities of an edge from the algorithm, without intermediate and indirect calculations. In fact, one of the advantages of the explicit model underlying RJaCGH [7] is the possibility of obtaining answers (in the form of statistics, posterior probabilities, etc) to the biologically relevant questions. Our original code was targeted to correctly classifying probes into the gained/lost/nochange status but we can, as well, focus the analysis on the probability that a probe is an edge. Moreover, it is easy to extend this approach to ask (and answer) more specific questions; for example, we could be interested in the probability that a probe is an edge between a state of nochange and a state of gain. In contrast, answers to these types of questions are often hard to obtain from other methods and the answers, if available, are rarely as immediately applicable as a probability. Finally, both our method and BioHMM [6] are unique among the methods compared because they can incorporate unequal distance between probes. With the data provided, the performance advantage of these two methods can not be detected since, by construction of the simulations, the interprobe distance is the same (or plays no role in the probability of change in state).
A broad issue raised by the paper of [1] and our reanalysis is why HMMbased models, as well as approaches such as CGHseg and Circular Binary Segmentation, do not achieve better performance with these data, especially given their excellent performance in other aCGH platforms [7, 20, 21]. The comparatively poor performance of these approaches with SNPbased data might be attributable more to specifics of the Affymetrix platform [11–13, 22–24] than to specific values of parameters related to noise in the data (as exemplified by Figure 3).
Response from original authors
Tianwei Yu & Xiaofeng Zhou
Address:
Department of Biostatistics, Rollins School of Public Health, Emory University, Atlanta, GA USACenter for Molecular Biology of Oral Diseases, College of Dentistry, University of Illinois at Chicago, Chicago, IL USAGuanghua School & Research Institute of Stomatology, Sun YatSen University, Guangzhou, China
Corresponding author: Xiaofeng Zhou
xfzhou@uic.edu
In our paper [1], the comparison study was done with a previous version of RJaCGH (version 1.0.0). The current version of RJaCGH (version 1.1.1) was publicly available only after our paper was already published. Two key parameters were nonexistent in the version 1.0.0 [25]. They are "normal.ref.percentile" and "normal.reference". The first one controls the sensitivity in edge detection, and the second one determines the expected value of the nonchanged clones.
As Rueda and DiazUriarte pointed out, two factors contributed to the apparent suboptimal performance of RJaCGH in our original paper [1]. The first is the expected value of the two copy clones being nonzero. It is a characteristic of copy number data processed by Copy Number Analysis Tool (CNAT) from Affymetrix Inc. In the version of RJaCGH we tested, there was no such parameter to adjust and its relevance would not have been known to the user. Obviously the RJaCGH package has been improved afterwards to add the parameter "normal.reference" to address this issue. The other two HMMbased packages already reached excellent performance without setting such a parameter [1]. We wish to point out the difficulty and importance of correctly setting this parameter in Affymetrix SNP arraybased copy number analysis. With the current Affymetrix SNP array platforms, the normal reference dataset was provided by an internal library, which is implemented as an integrated part in Affymetrix CNAT software [22]. While this approach greatly reduces the effort and cost to perform copy number analysis, it could also introduce bias from various sources. Hence even minimum variations in the experimental procedure may cause the median value of the two copy clones to drift from the ideal value. In addition, the X chromosome without copy number deviation from a male sample will yield copy numbers centered around 1, as opposed to 2 from the autosomes. These issues require special care by the user when a "normal.reference" value needs to be set.
The second factor contributing to the suboptimal performance was the substantially reduced number of iterations. Due to the high computational cost of the method (Table 2 of our paper) [1], we conducted simulations using reduced number of iterations based on our empirical observations on RJaCGH 1.0.0. As we listed in table 1 of our paper [1], the number of states was set to 3 when all five CNA segments are of the same copy number. This is different from what Rueda and DiazUriarte used in their current paper. It results in a relatively simple chain. Thus the impact of reduced iterations would be small for these cases. With the new version RJaCGH 1.1.1, we picked four scenarios where the package was successful and tested the effect of the reduced number of iterations using the code by Rueda and DiazUriarte. The performance achieved with the small number of iterations (Figure 4) is comparable to those reported in the paper by Rueda and DiazUriarte. Hence we believe in the cases where all five CNA segments share the same copy number, the suboptimal performance was mainly caused by the lack of the referencesetting "normal.reference" parameter and the tuning "normal.ref.percentile" parameter. Nonetheless, we agree that for the complex CNA cases, the reduced iterations will result in suboptimal performance.
The authors criticized us for conducting simulations using existing methods "not in the original formulation of their authors". We would like to point out that in Supplement Table 1 of our paper [1], the comparison of all the tested methods were performed with the default settings, except the number of permutations in DNAcopy and number of iterations in RJaCGH. In the results reported in Figure 3 of [1], modifications of the parameters were made in an effort to adapt them better to the SNP array data and improve their performance. Certainly this was done from a user's perspective and we could not guarantee optimality for every package tested. All the parameters we used were listed in Table 1 of our paper [1]. These manipulations were necessitated by the fact that copy number data generated by the Affymetrix arrays have different characteristics than traditional arrayCGH data. It would be beneficial if authors of the packages could provide users guidance as to how to optimize their packages for newer arrays. In general, we are happy that changes are now implemented in the new version of RJaCGH as targeted improvements. And it is encouraging to see the boosted performance of the method on SNP arraybased copy number data.
Abbreviations
 aCGH:

arraybased comparative genomic hybridization
 CBS:

aCGH analysis method developed by [2]
 CGHseg:

aCGH analysis method developed by [4]
 GLAD:

aCGH analysis method developed by [3]
 MCMC:

Markov Chain Monte Carlo
 oaCGH:

Oligonucleotide aCGH
 RJaCGH:

Reversible Jumpbased analysis of aCGH data developed by [7]
 ROC (curve):

Receiver operating characteristic (curve)
 SNP:

Single nucleotide polymorphism
References
 1.
Yu T, Ye H, Sun W, Li KC, Chen Z, Jacobs S, Bailey DK, Wong DT, Zhou X: A forwardbackward fragment assembling algorithm for the identification of genomic amplification and deletion breakpoints using highdensity single nucleotide polymorphism (SNP) array. BMC Bioinformatics 2007, 8: 145.
 2.
Olshen AB, Venkatraman ES, Lucito R, Wigler M: Circular binary segmentation for the analysis of arraybased DNA copy number data. Biostatistics 2004, 5: 557–572.
 3.
Hup'e P, Stransky N, Thiery JP, Radvanyi F, Barillot E: Analysis of array CGH data: from signal ratio to gain and loss of DNA regions. Bioinformatics 2004, 20: 3413–3422.
 4.
Picard F, Robin S, Lavielle M, Vaisse C, Daudin JJ: A statistical approach for array CGH data analysis. BMC Bioinformatics 2005, 6: 27.
 5.
Fridlyand J, Snijders AM, Pinkel D, Albertson DGa: Hidden Markov models approach to the analysis of array CGH data. Journal of Multivariate Analysis 2004, 90: 132–153.
 6.
Marioni JC, Thorne NP, Tavar'e S: BioHMM: a heterogeneous hidden Markov model for segmenting array CGH data. Bioinformatics 2006, 22: 1144–1146.
 7.
Rueda OM, DíazUriarte R: Flexible and accurate detection of genomic copynumber changes from aCGH. PLoS Comput Biol 2007, 3(6):e122.
 8.
Ylstra B, van den Ijssel P, Carvalho B, Brakenhoff RH, Meijer GA: BAC to the future! Or oligonucleotides: a perspective for micro array comparative genomic hybridization (array CGH). Nucleic Acids Res 2006, 34: 445–450.
 9.
Pinkel D, Albertson DG: Array comparative genomic hybridization and its applications in cancer. Nat Genet 2005, 37(Suppl):S11S17.
 10.
Lockwood WW, Chari R, Chi B, Lam WL: Recent advances in array comparative genomic hybridization technologies and their applications in human genetics. Eur J Hum Genet 2006, 14(2):139–148.
 11.
Huang J, Wei W, Chen J, Zhang J, Liu G, Di X, Mei R, Ishikawa S, Aburatani H, Jones KW, Shapero MH: CARAT: a novel method for allelic detection of DNA copy number changes using high density oligonucleotide arrays. BMC Bioinformatics 2006, 7.
 12.
Nannya Y, Sanada M, Nakazaki K, Hosoya N, Wang L, Hangaishi A, Kurokawa M, Chiba S, Bailey DK, Kennedy GC, Ogawa S: A robust algorithm for copy number detection using highdensity oligonucleotide single nucleotide polymorphism genotyping arrays. Cancer Res 2005, 65(14):6071–6079.
 13.
Wang W, Carvalho B, Miller N, Pevsner J, Chakravarti A, Irizarry R: Estimating GenomeWide Copy Number Using Allele Specific Mixture Models. Research in Computational Molecular Biology, Springer 2007, 137–150.
 14.
Gelman A, Carlin JB, Stern HS, Rubin DB: Bayesian Data Analysis. 2nd edition. Chapman & Hall/CRC; 2003.
 15.
Green P: Reversible jump Markov chain Monte Carlo computation and Bayesian model determination. Biometrika 1995, 7: 11–732.
 16.
Capp'e O, Moulines E, Ryden T: Inference in Hidden Markov Models (Springer Series in Statistics). Springer 2005.
 17.
Robert C, Ryden T, Titterington D: Bayesian inference in hidden Markov models through reversible jump Markov chain Monte Carlo. Journal of the Royal Statistical Society: Series B (Statistical Methodology) 2000, 62: 57–75.
 18.
Brooks S, Gelman A: General Methods for monitoring convergence of iterative simulations. Journal of Computational and Graphical Statistics 1998, 7: 434–455.
 19.
Scripts for analysis[http://ligarto.org/rdiaz/RcodereponseYuBMCBioinfo.tar.gz]
 20.
Willenbrock H, Fridlyand J: A comparison study: applying segmentation to array CGH data for downstream analyses. Bioinformatics 2005, 21: 4084–4091.
 21.
Lai WRR, Johnson MDD, Kucherlapati R, Park PJJ: Comparative analysis of algorithms for identifying amplifications and deletions in array CGH data. Bioinformatics 2005, 21: 3763–3770.
 22.
Huang J, Wei W, Zhang J, Liu G, Bignell GR, Stratton MR, Futreal PA, Wooster R, Jones KW, Shapero MH: Whole genome DNA copy number changes identified by high density oligonucleotide arrays. Hum Genomics 2004, 1(4):287–299.
 23.
Zhao X, Li C, Paez JG, Chin K, Jänne PA, Chen TH, Girard L, Minna J, Christiani D, Leo C, Gray JW, Sellers WR, Meyerson M: An integrated view of copy number and allelic alterations in the cancer genome using single nucleotide polymorphism arrays. Cancer Res 2004, 64(9):3060–3071.
 24.
Lai Y, Zhao H: A statistical method to detect chromosomal regions with DNA copy number alterations using SNParraybased CGH data. Comput Biol Chem 2005, 29: 47–54.
 25.
Rueda OM, DiazUriarte R: A flexible, accurate and extensible statistical method for detecting genomic copynumber changes. COBRA Preprint Series 2006., 9:
Acknowledgements
X. Zhou and, particularly, T. Yu for explanations and details of their simulations. Two reviewers for comments on the ms.
Funding provided by Fundacion de Investigacion Medica Mutua Madrilena. R.D.U. is partially supported by the Ramon y Cajal programme of the Spanish MEC. Funding bodies had no role in study design, in the collection, analysis, and interpretation of data, in the writing of the manuscript or in the decision to submit the manuscript for publication.
Author information
Affiliations
Corresponding authors
Additional information
Authors' contributions
OMR implemented most of the original method. RDU drafted the MS and carried out most comparisons. Both authors modified and approved the ms.
Authors’ original submitted files for images
Below are the links to the authors’ original submitted files for images.
Rights and permissions
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.
About this article
Cite this article
Rueda, O.M., DiazUriarte, R. A response to Yu et al. "A forwardbackward fragment assembling algorithm for the identification of genomic amplification and deletion breakpoints using highdensity single nucleotide polymorphism (SNP) array", BMC Bioinformatics 2007, 8: 145. BMC Bioinformatics 8, 394 (2007). https://doi.org/10.1186/147121058394
Received:
Accepted:
Published:
Keywords
 Markov Chain Monte Carlo
 Hide State
 Markov Chain Monte Carlo Algorithm
 Viterbi Algorithm
 Single Nucleotide Polymorphism Array