Literature DB >> 31397844

MsPAC: a tool for haplotype-phased structural variant detection.

Oscar L Rodriguez1, Anna Ritz2, Andrew J Sharp1, Ali Bashir1.   

Abstract

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 potential for far more comprehensive views of individual genomes. Here, we present MsPAC, a tool that combines both technologies to partition reads, assemble haplotypes (via existing software) and convert assemblies into high-quality, phased SV predictions. MsPAC represents a framework for haplotype-resolved SV calls that moves one step closer to fully resolved, diploid genomes.
AVAILABILITY AND IMPLEMENTATION: https://github.com/oscarlr/MsPAC. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
© The Author(s) 2019. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Mesh:

Year:  2020        PMID: 31397844      PMCID: PMC7523683          DOI: 10.1093/bioinformatics/btz618

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


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