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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Shetty, Amol Carl, Athri, Prashanth, Mondal, Kajari, Horner, Vanessa L, Steinberg, Karyn Meltz, Patel, Viren, Caspary, Tamara, Cutler, David J, Zwick, Michael E
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: BioMed Central 2010
Gaiak:
Software
Sarrera elektronikoa: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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