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iSVP: an integrated structural variant calling pipeline from high-throughput sequencing data
BACKGROUND: Structural variations (SVs), such as insertions, deletions, inversions, and duplications, are a common feature in human genomes, and a number of studies have reported that such SVs are associated with human diseases. Although the progress of next generation sequencing (NGS) technologies...
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| Main Authors: | , , , , , , , |
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| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
BioMed Central
2013
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4029547/ https://ncbi.nlm.nih.gov/pubmed/24564972 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1752-0509-7-S6-S8 |
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