BMC Genomics · 2012 · 347 citations · 34 references
Life SciencesBioinformaticsMolecular GeneticsComputational PhenotypingGenomic Data AnalysisGenomicsCancer GenomicsCopy Number AlterationsDna SequencingChromosomal Copy Number AnalysisCopy Number ChangesCopy Number Variant SegmentationGenome-wide Copy Number AnalysisNext-generation Sequencing Based Copy Number AnalysisNext-generation Sequencing Copy Number AnalysisNext-generation Sequencing-based Copy Number AnalysisSnp Arrays
BACKGROUND: Cancer progression is associated with genomic instability and an accumulation of gains and losses of DNA. The growing variety of tools for measuring genomic copy numbers, including various types of array-CGH, SNP arrays and high-throughput sequencing, calls for a coherent framework offering unified and consistent handling of single- and multi-track segmentation problems. In addition, there is a demand for highly computationally efficient segmentation algorithms, due to the emergence of very high density scans of copy number. RESULTS: A comprehensive Bioconductor package for copy number analysis is presented. The package offers a unified framework for single sample, multi-sample and multi-track segmentation and is based on statistically sound penalized least squares principles. Conditional on the number of breakpoints, the estimates are optimal in the least squares sense. A novel and computationally highly efficient algorithm is proposed that utilizes vector-based operations in R. Three case studies are presented. CONCLUSIONS: The R package copynumber is a software suite for segmentation of single- and multi-track copy number data using algorithms based on coherent least squares principles.
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The landscape of somatic copy-number alteration across human cancers
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Modern Applied Statistics with S-Plus.
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