Cancer Program Publication

High-resolution mapping of copy-number alterations with massively parallel sequencing
ProjectBioinformatics & Computational Biology
AbstractCancer results from somatic alterations in key genes, including point mutations, copy number alterations and structural rearrangements. A powerful way to discover cancer-causing genes is to identify genomic regions that show recurrent copy-number alterations (gains and losses) in tumor genomes. Recent advances in sequencing technologies suggest that massively parallel sequencing may provide a feasible alternative to DNA microarrays for detecting copy-number alterations. Here, we present: (i) a statistical analysis of the power to detect copy-number alterations of a given size; (ii) SegSeq, an algorithm to identify chromosomal breakpoints using massively parallel sequence data; and (iii) analysis of experimental data from three matched pairs of tumor and normal cell lines. We show that a collection of ~14 million aligned sequence reads from human cell lines has comparable power to detect events as the current generation of DNA microarrays and has over two-fold better precision for localizing breakpoints (typically, to within ~1 kb).
AuthorsDerek Y. Chiang, Gad Getz, David B. Jaffe, Michael J.T. O'Kelly, Xiaojun Zhao, Scott L. Carter, Carsten Russ, Chad Nusbaum, Matthew Meyerson, Eric S. Lander
Publication Date01/01/2009
Contact emails dchiang@broad.mit.edu
gadgetz@broad.mit.edu
Publication URLhttp://www.nature.com/nmeth/journal/v6/n1/abs/nmeth.1276.html
CitationNature Methods 6:99-103
Keywordscopy-number alterations; next-generation sequencing; segmentation algorithm; tumor genome characterization
 
Supplemental Information
Files
DescriptionFile
Alignment positions of sequence reads (hg18)arachne_qltout_marks.tar.gz
Matlab files with alignable coordinateshg18_alignable_N36_D2.tar.gz
Matlab source code, SegSeq version 1.0.1SegSeq_1.0.1.tar.gz