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Structural variant analysis for linked-read sequencing data with gemtools
SUMMARY: Linked-read sequencing generates synthetic long reads which are useful for the detection and analysis of structural variants (SVs). The software associated with 10× Genomics linked-read sequencing, Long Ranger, generates the essential output files (BAM, VCF, SV BEDPE) necessary for downstre...
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| Publicat a: | Bioinformatics |
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| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6821325/ https://ncbi.nlm.nih.gov/pubmed/30938757 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btz239 |
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