SeqAnt: A web service to rapidly identify and annotate DNA sequence variations
<p>Abstract</p> <p>Background</p> <p>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...
Main Authors: | Patel Viren, Steinberg Karyn, Horner Vanessa L, Mondal Kajari, Athri Prashanth, Shetty Amol, Caspary Tamara, Cutler David J, Zwick Michael E |
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Format: | Article |
Language: | English |
Published: |
BMC
2010-09-01
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Series: | BMC Bioinformatics |
Online Access: | http://www.biomedcentral.com/1471-2105/11/471 |
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