This article is part of the supplement: Selected articles from the IEEE International Workshop on Genomic Signal Processing and Statistics (GENSIPS) 2011

Open Access Research

Effective normalization for copy number variation detection from whole genome sequencing

Angel Janevski*, Vinay Varadan, Sitharthan Kamalakaran, Nilanjana Banerjee and Nevenka Dimitrova*

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Philips Research, 345 Scarborough Rd, Briarcliff Manor, NY 10510, USA

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BMC Genomics 2012, 13(Suppl 6):S16  doi:10.1186/1471-2164-13-S6-S16

Published: 26 October 2012

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Additional file 1:

FREEC normalization options. Normalization in FREEC.

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Additional file 2:

Supplementary figures and tables. Additional figures and tables referenced in the main document.

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