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inGAP-sv: a novel scheme to identify and visualize structural variation from paired end mapping data
Mining genetic variation from personal genomes is a crucial step towards investigating the relationship between genotype and phenotype. However, compared to the detection of SNPs and small indels, characterizing large and particularly complex structural variation is much more difficult and less intu...
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| 主要な著者: | , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Oxford University Press
2011
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3125812/ https://ncbi.nlm.nih.gov/pubmed/21715388 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkr506 |
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