SLMSuite: a suite of algorithms for segmenting genomic profiles

SLMSuite: a suite of algorithms for segmenting genomic profiles

Abstract Background The identification of copy number variants (CNVs) is essential to study human genetic variation and to understand the genetic basis of mendelian disorders and cancers. At present, genome-wide detection of CNVs can be achieved using microarray or second generation sequencing (SGS)...

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Bibliographic Details
Main Authors: Valerio Orlandini, Aldesia Provenzano, Sabrina Giglio, Alberto Magi
Format: Article
Language:English
Published: BMC 2017-06-01
Series:BMC Bioinformatics
Subjects:
Software
Genomics
Bioinformatics
SLM
Online Access:http://link.springer.com/article/10.1186/s12859-017-1734-5

Internet

http://link.springer.com/article/10.1186/s12859-017-1734-5

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