An initial map of insertion and deletion (INDEL) variation in the human genome

Although many studies have been conducted to identify single nucleotide polymorphisms (SNPs) in humans, few studies have been conducted to identify alternative forms of natural genetic variation, such as insertion and deletion (INDEL) polymorphisms. In this report, we describe an initial map of huma...

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Detalhes bibliográficos
Main Authors: Mills, Ryan E., Luttig, Christopher T., Larkins, Christine E., Beauchamp, Adam, Tsui, Circe, Pittard, W. Stephen, Devine, Scott E.
Formato: Artigo
Idioma:Inglês
Publicado em: Cold Spring Harbor Laboratory Press 2006
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1557762/
https://ncbi.nlm.nih.gov/pubmed/16902084
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gr.4565806
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