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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Detalles Bibliográficos
Autores principales: Shetty, Amol Carl, Athri, Prashanth, Mondal, Kajari, Horner, Vanessa L, Steinberg, Karyn Meltz, Patel, Viren, Caspary, Tamara, Cutler, David J, Zwick, Michael E
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Software
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2955049/
https://www.ncbi.nlm.nih.gov/pubmed/20854673
http://dx.doi.org/10.1186/1471-2105-11-471

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2955049/
https://www.ncbi.nlm.nih.gov/pubmed/20854673
http://dx.doi.org/10.1186/1471-2105-11-471

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