1. Substantial biases in ultra-short read data sets from high-throughput DNA sequencing;Dohm;Nucleic Acids Res.,2008
2. High-resolution mapping of copy-number alterations with massively parallel sequencing;Chiang;Nat. Methods,2008
3. A large genome center's improvements to the Illumina sequencing system;Quail;Nat. Methods,2008
4. CNAseg—a novel framework for identification of copy number changes in cancer from second-generation sequencing data;Ivakhno;Bioinformatics,2010
5. Sensitive and accurate detection of copy number variants using read depth of coverage;Yoon;Genome Res.,2009