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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Bibliografiset tiedot
Päätekijät: Mills, Ryan E., Luttig, Christopher T., Larkins, Christine E., Beauchamp, Adam, Tsui, Circe, Pittard, W. Stephen, Devine, Scott E.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Cold Spring Harbor Laboratory Press 2006
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Resource
Linkit: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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