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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Bibliografiset tiedot
Päätekijät: Dalca, Adrian V., Rumble, Stephen M., Levy, Samuel, Brudno, Michael
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Oxford University Press 2010
Aiheet:
Ismb 2010 Conference Proceedings July 11 to July 13, 2010, Boston, Ma, Usa
Linkit: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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