SeqAnt: A web service to rapidly identify and annotate DNA sequence variations

BACKGROUND: The enormous throughput and low cost of second-generation sequencing platforms now allow research and clinical geneticists to routinely perform single experiments that identify tens of thousands to millions of variant sites. Existing methods to annotate variant sites using information fr...

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Bibliografiska uppgifter
Huvudupphovsmän: Shetty, Amol Carl, Athri, Prashanth, Mondal, Kajari, Horner, Vanessa L, Steinberg, Karyn Meltz, Patel, Viren, Caspary, Tamara, Cutler, David J, Zwick, Michael E
Materialtyp: Artigo
Språk:Inglês
Publicerad: BioMed Central 2010
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Software
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC2955049/
https://ncbi.nlm.nih.gov/pubmed/20854673
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2105-11-471
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