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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...
Tallennettuna:
| Päätekijät: | , , , , , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BioMed Central
2010
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| Aiheet: | |
| Linkit: | 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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