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DELLY: structural variant discovery by integrated paired-end and split-read analysis
Motivation: The discovery of genomic structural variants (SVs) at high sensitivity and specificity is an essential requirement for characterizing naturally occurring variation and for understanding pathological somatic rearrangements in personal genome sequencing data. Of particular interest are int...
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| Autors principals: | , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2012
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3436805/ https://ncbi.nlm.nih.gov/pubmed/22962449 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/bts378 |
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