An integrative probabilistic model for identification of structural variation in sequencing data

Paired-end sequencing is a common approach for identifying structural variation (SV) in genomes. Discrepancies between the observed and expected alignments indicate potential SVs. Most SV detection algorithms use only one of the possible signals and ignore reads with multiple alignments. This result...

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Bibliografiske detaljer
Main Authors: Sindi, Suzanne S, Önal, Selim, Peng, Luke C, Wu, Hsin-Ta, Raphael, Benjamin J
Format: Artigo
Sprog:Inglês
Udgivet: BioMed Central 2012
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Method
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3439973/
https://ncbi.nlm.nih.gov/pubmed/22452995
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/gb-2012-13-3-r22
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