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MsPAC: a tool for haplotype-phased structural variant detection
SUMMARY: While next-generation sequencing (NGS) has dramatically increased the availability of genomic data, phased genome assembly and structural variant (SV) analyses are limited by NGS read lengths. Long-read sequencing from Pacific Biosciences and NGS barcoding from 10x Genomics hold the potenti...
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| Publicado no: | Bioinformatics |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7523683/ https://ncbi.nlm.nih.gov/pubmed/31397844 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btz618 |
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