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Comprehensive evaluation and characterisation of short read general-purpose structural variant calling software
In recent years, many software packages for identifying structural variants (SVs) using whole-genome sequencing data have been released. When published, a new method is commonly compared with those already available, but this tends to be selective and incomplete. The lack of comprehensive benchmarki...
Shranjeno v:
| izdano v: | Nat Commun |
|---|---|
| Main Authors: | , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Nature Publishing Group UK
2019
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6642177/ https://ncbi.nlm.nih.gov/pubmed/31324872 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41467-019-11146-4 |
| Oznake: |
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