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Detection and characterization of novel sequence insertions using paired-end next-generation sequencing

Motivation: In the past few years, human genome structural variation discovery has enjoyed increased attention from the genomics research community. Many studies were published to characterize short insertions, deletions, duplications and inversions, and associate copy number variants (CNVs) with di...

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Detalhes bibliográficos
Main Authors: Hajirasouliha, Iman, Hormozdiari, Fereydoun, Alkan, Can, Kidd, Jeffrey M., Birol, Inanc, Eichler, Evan E., Sahinalp, S. Cenk
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2010
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2865866/
https://ncbi.nlm.nih.gov/pubmed/20385726
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btq152
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