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PolyScan: An automatic indel and SNP detection approach to the analysis of human resequencing data

Small insertions and deletions (indels) and single nucleotide polymorphisms (SNPs) are common genetic variants that are thought to be associated with a wide variety of human diseases. Owing to the genome’s size and complexity, manually characterizing each one of these variations in an individual is...

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Bibliografski detalji
Glavni autori: Chen, Ken, McLellan, Michael D., Ding, Li, Wendl, Michael C., Kasai, Yumi, Wilson, Richard K., Mardis, Elaine R.
Format: Artigo
Jezik:Inglês
Izdano: Cold Spring Harbor Laboratory Press 2007
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1855178/
https://ncbi.nlm.nih.gov/pubmed/17416743
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gr.6151507
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