This article is part of the supplement: Selected articles from the IEEE International Workshop on Genomic Signal Processing and Statistics (GENSIPS) 2011
Effective normalization for copy number variation detection from whole genome sequencing
Philips Research, 345 Scarborough Rd, Briarcliff Manor, NY 10510, USA
BMC Genomics 2012, 13(Suppl 6):S16 doi:10.1186/1471-2164-13-S6-S16Published: 26 October 2012
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FREEC normalization options. Normalization in FREEC.
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