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Longshot enables accurate variant calling in diploid genomes from single-molecule long read sequencing
Whole-genome sequencing using sequencing technologies such as Illumina enables the accurate detection of small-scale variants but provides limited information about haplotypes and variants in repetitive regions of the human genome. Single-molecule sequencing (SMS) technologies such as Pacific Biosci...
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| Pubblicato in: | Nat Commun |
|---|---|
| Autori principali: | , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Nature Publishing Group UK
2019
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6788989/ https://ncbi.nlm.nih.gov/pubmed/31604920 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41467-019-12493-y |
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