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VARiD: A variation detection framework for color-space and letter-space platforms

Motivation: High-throughput sequencing (HTS) technologies are transforming the study of genomic variation. The various HTS technologies have different sequencing biases and error rates, and while most HTS technologies sequence the residues of the genome directly, generating base calls for each posit...

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Bibliografische gegevens
Hoofdauteurs: Dalca, Adrian V., Rumble, Stephen M., Levy, Samuel, Brudno, Michael
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Oxford University Press 2010
Onderwerpen:
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2881369/
https://ncbi.nlm.nih.gov/pubmed/20529926
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btq184
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