Rapid detection of structural variation in a human genome using nanochannel-based genome mapping technology

BACKGROUND: Structural variants (SVs) are less common than single nucleotide polymorphisms and indels in the population, but collectively account for a significant fraction of genetic polymorphism and diseases. Base pair differences arising from SVs are on a much higher order (>100 fold) than poi...

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Bibliografski detalji
Izdano u:Gigascience
Glavni autori: Cao, Hongzhi, Hastie, Alex R, Cao, Dandan, Lam, Ernest T, Sun, Yuhui, Huang, Haodong, Liu, Xiao, Lin, Liya, Andrews, Warren, Chan, Saki, Huang, Shujia, Tong, Xin, Requa, Michael, Anantharaman, Thomas, Krogh, Anders, Yang, Huanming, Cao, Han, Xu, Xun
Format: Artigo
Jezik:Inglês
Izdano: BioMed Central 2014
Teme:
Research
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4322599/
https://ncbi.nlm.nih.gov/pubmed/25671094
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/2047-217X-3-34
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