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Estimating the information value of polymorphic sites using pooled sequences

BACKGROUND: High-throughput sequencing is a cost effective method for identifying genetic variation, and it is currently in use on a large scale across the field of biology, including ecology and population genetics. Correctly identifying variable sites and allele frequencies from sequencing data re...

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Detalhes bibliográficos
Publicado no:BMC Genomics
Autor principal: Malde, Ketil
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2014
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4239578/
https://ncbi.nlm.nih.gov/pubmed/25571927
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-15-S6-S20
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