Your browser doesn't support javascript.
loading
HaplotypeTools: a toolkit for accurately identifying recombination and recombinant genotypes.
Farrer, Rhys A.
Afiliação
  • Farrer RA; Medical Research Council Centre for Medical Mycology at the University of Exeter, Exeter, UK. r.farrer@exeter.ac.uk.
BMC Bioinformatics ; 22(1): 560, 2021 Nov 22.
Article em En | MEDLINE | ID: mdl-34809571
ABSTRACT

BACKGROUND:

Identifying haplotypes is central to sequence analysis in diploid or polyploid genomes. Despite this, there remains a lack of research and tools designed for physical phasing and its downstream analysis.

RESULTS:

HaplotypeTools is a new toolset to phase variant sites using VCF and BAM files and to analyse phased VCFs. Phasing is achieved via the identification of reads overlapping ≥ 2 heterozygous positions and then extended by additional reads, a process that can be parallelized across a computer cluster. HaplotypeTools includes various utility scripts for downstream analysis including crossover detection and phylogenetic placement of haplotypes to other lineages or species. HaplotypeTools was assessed for accuracy against WhatsHap using simulated short and long reads, demonstrating higher accuracy, albeit with reduced haplotype length. HaplotypeTools was also tested on real Illumina data to determine the ancestry of hybrid fungal isolate Batrachochytrium dendrobatidis (Bd) SA-EC3, finding 80% of haplotypes across the genome phylogenetically cluster with parental lineages BdGPL (39%) and BdCAPE (41%), indicating those are the parental lineages. Finally, ~ 99% of phasing was conserved between overlapping phase groups between SA-EC3 and either parental lineage, indicating mitotic gene conversion/parasexuality as the mechanism of recombination for this hybrid isolate. HaplotypeTools is open source and freely available from https//github.com/rhysf/HaplotypeTools under the MIT License.

CONCLUSIONS:

HaplotypeTools is a powerful resource for analyzing hybrid or recombinant diploid or polyploid genomes and identifying parental ancestry for sub-genomic regions.
Assuntos
Palavras-chave

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Genômica / Sequenciamento de Nucleotídeos em Larga Escala Tipo de estudo: Prognostic_studies Idioma: En Revista: BMC Bioinformatics Assunto da revista: INFORMATICA MEDICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Genômica / Sequenciamento de Nucleotídeos em Larga Escala Tipo de estudo: Prognostic_studies Idioma: En Revista: BMC Bioinformatics Assunto da revista: INFORMATICA MEDICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Reino Unido