VarScan: variant detection in massively parallel sequencing of individual and pooled samples

Summary: Massively parallel sequencing technologies hold incredible promise for the study of DNA sequence variation, particularly the identification of variants affecting human disease. The unprecedented throughput and relatively short read lengths of Roche/454, Illumina/Solexa, and other platforms...

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Bibliografiska uppgifter
Huvudupphovsmän: Koboldt, Daniel C., Chen, Ken, Wylie, Todd, Larson, David E., McLellan, Michael D., Mardis, Elaine R., Weinstock, George M., Wilson, Richard K., Ding, Li
Materialtyp: Artigo
Språk:Inglês
Publicerad: Oxford University Press 2009
Ämnen:
Applications Note
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC2734323/
https://ncbi.nlm.nih.gov/pubmed/19542151
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btp373
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