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Read count-based method for high-throughput allelic genotyping of transposable elements and structural variants

BACKGROUND: Like other structural variants, transposable element insertions can be highly polymorphic across individuals. Their functional impact, however, remains poorly understood. Current genome-wide approaches for genotyping insertion-site polymorphisms based on targeted or whole-genome sequenci...

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Détails bibliographiques
Publié dans:BMC Genomics
Auteurs principaux: Kuhn, Alexandre, Ong, Yao Min, Quake, Stephen R., Burkholder, William F.
Format: Artigo
Langue:Inglês
Publié: BioMed Central 2015
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Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC4494700/
https://ncbi.nlm.nih.gov/pubmed/26153459
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12864-015-1700-4
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