8 research outputs found

    A Faster Circular Binary Segmentation Algorithm for the Analysis of Array CGH Data

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    Motivation: Array CGH technologies enable the simultaneous measurement of DNA copy number for thousands of sites on a genome. We developed the circular binary segmentation (CBS) algorithm to divide the genome into regions of equal copy number (Olshen {\it et~al}, 2004). The algorithm tests for change-points using a maximal tt-statistic with a permutation reference distribution to obtain the corresponding pp-value. The number of computations required for the maximal test statistic is O(N2),O(N^2), where NN is the number of markers. This makes the full permutation approach computationally prohibitive for the newer arrays that contain tens of thousands markers and highlights the need for a faster. algorithm. Results: We present a hybrid approach to obtain the pp-value of the test statistic in linear time. We also introduce a rule for stopping early when there is strong evidence for the presence of a change. We show through simulations that the hybrid approach provides a substantial gain in speed with only a negligible loss in accuracy and that the stopping rule further increases speed. We also present the analysis of array CGH data from a breast cancer cell line to show the impact of the new approaches on the analysis of real data. Availability: An R (R Development Core Team, 2006) version of the CBS algorithm has been implemented in the ``DNAcopy\u27\u27 package of the Bioconductor project (Gentleman {\it et~al}, 2004). The proposed hybrid method for the pp-value is available in version 1.2.1 or higher and the stopping rule for declaring a change early is available in version 1.5.1 or higher

    Gene expression studies from basic research to the clinic

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    Analysis and visualization of chromosomal abnormalities in SNP data with SNPscan-7

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    <p><b>Copyright information:</b></p><p>Taken from "Analysis and visualization of chromosomal abnormalities in SNP data with SNPscan"</p><p>BMC Bioinformatics 2006;7():25-25.</p><p>Published online 18 Jan 2006</p><p>PMCID:PMC1382255.</p><p></p>16 of 23 cells revealed a deletion (an example is shown in A), while the remainder appeared euploid (B)
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