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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Main Authors: Shetty, Amol Carl, Athri, Prashanth, Mondal, Kajari, Horner, Vanessa L, Steinberg, Karyn Meltz, Patel, Viren, Caspary, Tamara, Cutler, David J, Zwick, Michael E
Formáid: Artigo
Teanga:Inglês
Foilsithe: BioMed Central 2010
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Software
Rochtain Ar Líne: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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