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Identifying structural variants using linked-read sequencing data
MOTIVATION: Structural variation, including large deletions, duplications, inversions, translocations and other rearrangements, is common in human and cancer genomes. A number of methods have been developed to identify structural variants from Illumina short-read sequencing data. However, reliable i...
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| Publicat a: | Bioinformatics |
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| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2018
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5860216/ https://ncbi.nlm.nih.gov/pubmed/29112732 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btx712 |
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