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...

Celý popis

Uloženo v:
Podrobná bibliografie
Hlavní autoři: Shetty, Amol Carl, Athri, Prashanth, Mondal, Kajari, Horner, Vanessa L, Steinberg, Karyn Meltz, Patel, Viren, Caspary, Tamara, Cutler, David J, Zwick, Michael E
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2010
Témata:
Software
On-line přístup: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
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!

Podobné jednotky