SegSeq 1.01 – Detect CNVs from Short Sequence Reads

SegSeq 1.01

:: DESCRIPTION

SegSeq is an algorithm to identify chromosomal breakpoints using massively parallel sequence data

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::DEVELOPER

the Broad Institute

:: SCREENSHOTS

N/A

:: REQUIREMENTS

:: DOWNLOAD

 SegSeq

:: MORE INFORMATION

Citation:

Nat Methods. 2009 Jan;6(1):99-103. Epub 2008 Nov 30.
High-resolution mapping of copy-number alterations with massively parallel sequencing.
Chiang DY, Getz G, Jaffe DB, O’Kelly MJ, Zhao X, Carter SL, Russ C, Nusbaum C, Meyerson M, Lander ES.

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