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MAC: identifying and correcting annotation for multi-nucleotide variations
BACKGROUND: Next-Generation Sequencing (NGS) technologies have rapidly advanced our understanding of human variation in cancer. To accurately translate the raw sequencing data into practical knowledge, annotation tools, algorithms and pipelines must be developed that keep pace with the rapidly evolv...
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| Pubblicato in: | BMC Genomics |
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| Autori principali: | , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BioMed Central
2015
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4521406/ https://ncbi.nlm.nih.gov/pubmed/26231518 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12864-015-1779-7 |
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