Literature DB >> 24307702

HomSI: a homozygous stretch identifier from next-generation sequencing data.

Zeliha Görmez1, Burcu Bakir-Gungor, Mahmut Samil Sagiroglu.   

Abstract

UNLABELLED: In consanguineous families, as a result of inheriting the same genomic segments through both parents, the individuals have stretches of their genomes that are homozygous. This situation leads to the prevalence of recessive diseases among the members of these families. Homozygosity mapping is based on this observation, and in consanguineous families, several recessive disease genes have been discovered with the help of this technique. The researchers typically use single nucleotide polymorphism arrays to determine the homozygous regions and then search for the disease gene by sequencing the genes within this candidate disease loci. Recently, the advent of next-generation sequencing enables the concurrent identification of homozygous regions and the detection of mutations relevant for diagnosis, using data from a single sequencing experiment. In this respect, we have developed a novel tool that identifies homozygous regions using deep sequence data. Using *.vcf (variant call format) files as an input file, our program identifies the majority of homozygous regions found by microarray single nucleotide polymorphism genotype data.
AVAILABILITY AND IMPLEMENTATION: HomSI software is freely available at www.igbam.bilgem.tubitak.gov.tr/softwares/HomSI, with an online manual.

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Mesh:

Year:  2013        PMID: 24307702     DOI: 10.1093/bioinformatics/btt686

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


  12 in total

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Journal:  Mol Biol Rep       Date:  2021-01-03       Impact factor: 2.316

3.  Myophosphorylase (PYGM) mutations determined by next generation sequencing in a cohort from Turkey with McArdle disease.

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Journal:  Neuromuscul Disord       Date:  2017-06-16       Impact factor: 4.296

4.  Uniparental isodisomy of chromosome 2 causing MRPL44-related multisystem mitochondrial disease.

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5.  Rapid Detection of Rare Deleterious Variants by Next Generation Sequencing with Optional Microarray SNP Genotype Data.

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Journal:  Hum Mutat       Date:  2015-07-22       Impact factor: 4.878

6.  Whole exome sequencing and methylation‑specific multiplex ligation‑dependent probe amplification applied to identify Angelman syndrome due to paternal uniparental disomy in two unrelated patients.

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Authors:  M Yaro; K A Munyard; E Morgan; R J N Allcock; M J Stear; D M Groth
Journal:  BMC Genomics       Date:  2019-11-07       Impact factor: 3.969

8.  Improved Diagnosis of Rare Disease Patients through Systematic Detection of Runs of Homozygosity.

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Journal:  J Mol Diagn       Date:  2020-06-30       Impact factor: 5.568

9.  Novel mutations in genes causing hereditary spastic paraplegia and Charcot-Marie-Tooth neuropathy identified by an optimized protocol for homozygosity mapping based on whole-exome sequencing.

Authors:  Daliya Kancheva; Derek Atkinson; Peter De Rijk; Magdalena Zimon; Teodora Chamova; Vanyo Mitev; Ahmet Yaramis; Gian Maria Fabrizi; Haluk Topaloglu; Ivailo Tournev; Yesim Parman; Yesim Parma; Esra Battaloglu; Alejandro Estrada-Cuzcano; Albena Jordanova
Journal:  Genet Med       Date:  2015-10-22       Impact factor: 8.822

10.  Multifocal gastric adenocarcinoma in a patient with LRBA deficiency.

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