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Collapsed haplotype pattern method for linkage analysis of next-generation sequence data

Collapsed haplotype pattern method for linkage analysis of next-generation sequence data

http://www.wikidata.org/entity/Q30931839

about

Genetic linkage analysis in the age of whole-genome sequencing Generation of sequence-based data for pedigree-segregating Mendelian or Complex traits.Construction of relatedness matrices using genotyping-by-sequencing data.Caucasian Families Exhibit Significant Linkage of Myopia to Chromosome 11p.Can whole-exome sequencing data be used for linkage analysis?Parametric Linkage Analysis Identifies Five Novel Genome-Wide Significant Loci for Familial Lung Cancer.PERCH: A Unified Framework for Disease Gene Prioritization.Whole Exome Sequencing Identify the 6q12-q16 Linkage Region and a Candidate Gene TTK for Pulmonary Nontuberculous Mycobacterial Disease.Myopia in Chinese families shows linkage to 10q26.13.

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Collapsed haplotype pattern method for linkage analysis of next-generation sequence data

http://www.wikidata.org/entity/Q30931839

description

2015 nî lūn-bûn

@nan

2015 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

2015 թվականի ապրիլին հրատարակված գիտական հոդված

@hy

2015年の論文

@ja

2015年論文

@yue

2015年論文

@zh-hant

2015年論文

@zh-hk

2015年論文

@zh-mo

2015年論文

@zh-tw

2015年论文

@wuu

name

Collapsed haplotype pattern method for linkage analysis of next-generation sequence data

@ast

Collapsed haplotype pattern method for linkage analysis of next-generation sequence data

@en

type

label

Collapsed haplotype pattern method for linkage analysis of next-generation sequence data

@ast

Collapsed haplotype pattern method for linkage analysis of next-generation sequence data

@en

prefLabel

Collapsed haplotype pattern method for linkage analysis of next-generation sequence data

@ast

Collapsed haplotype pattern method for linkage analysis of next-generation sequence data

@en

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European Journal of Human Genetics

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Collapsed haplotype pattern method for linkage analysis of next-generation sequence data

@en

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Biao Li

http://www.w3.org/2001/XMLSchema#string

Di Zhang

http://www.w3.org/2001/XMLSchema#string

Gao T Wang

http://www.w3.org/2001/XMLSchema#string

Hang Dai

http://www.w3.org/2001/XMLSchema#string

Suzanne M Leal

http://www.w3.org/2001/XMLSchema#string

P2860

Handling marker-marker linkage disequilibrium: pedigree analysis with clustered markers

Exome sequencing identifies the cause of a mendelian disorder

Strategies for multilocus linkage analysis in humans

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

Parametric and nonparametric linkage analysis: a unified multipoint approach

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

Faster sequential genetic linkage computations

Mutations in KARS, encoding lysyl-tRNA synthetase, cause autosomal-recessive nonsyndromic hearing impairment DFNB89

Mega2: data-handling for facilitating genetic linkage and association analyses.

Ignoring intermarker linkage disequilibrium induces false-positive evidence of linkage for consanguineous pedigrees when genotype data is missing for any pedigree member.

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1739-1743

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scholarly article

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10.1038/EJHG.2015.64

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12

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23

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2015-04-15T00:00:00Z

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4795207

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