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Savant: genome browser for high-throughput sequencing data
Motivation: The advent of high-throughput sequencing (HTS) technologies has made it affordable to sequence many individuals' genomes. Simultaneously the computational analysis of the large volumes of data generated by the new sequencing machines remains a challenge. While a plethora of tools ar...
Tallennettuna:
| Päätekijät: | , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Oxford University Press
2010
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3271355/ https://ncbi.nlm.nih.gov/pubmed/20562449 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btq332 |
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