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HapCHAT: adaptive haplotype assembly for efficiently leveraging high coverage in long reads
BACKGROUND: Haplotype assembly is the process of assigning the different alleles of the variants covered by mapped sequencing reads to the two haplotypes of the genome of a human individual. Long reads, which are nowadays cheaper to produce and more widely available than ever before, have been used...
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| Pubblicato in: | BMC Bioinformatics |
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| Autori principali: | , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BioMed Central
2018
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6029272/ https://ncbi.nlm.nih.gov/pubmed/29970002 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-018-2253-8 |
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