MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes (Q24635938)

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Language	Label	Description	Also known as
English	MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes	scientific article

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scholarly article

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MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes (English)

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4

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Cristen J. Willer

object named as

Cristen J Willer

2

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1

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Yun Li

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author name string

Jun Ding

3

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Gonçalo R Abecasis

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language of work or name

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publication date

December 2010

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Genetic Epidemiology

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34

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8

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816-34

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Six new loci associated with body mass index highlight a neuronal influence on body weight regulation

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Mapping short DNA sequencing reads and calling variants using mapping quality scores

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7 April 2017

A second generation human haplotype map of over 3.1 million SNPs

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PLINK: a tool set for whole-genome association and population-based linkage analyses

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A fast and flexible statistical model for large-scale population genotype data: applications to inferring missing genotypes and haplotypic phase

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A haplotype map of the human genome

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The Sequence Alignment/Map format and SAMtools

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

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A New Statistical Method for Haplotype Reconstruction from Population Data

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7 April 2017

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1 reference

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Genotype imputation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3175618

7 April 2017

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1 reference

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1 reference

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1 reference

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Assessment of genotype imputation methods

1 reference

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Genotype-imputation accuracy across worldwide human populations

1 reference

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Analyses and comparison of accuracy of different genotype imputation methods

1 reference

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Comprehensive association study of type 2 diabetes and related quantitative traits with 222 candidate genes

1 reference

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Common variants in the GDF5-UQCC region are associated with variation in human height

1 reference

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1 reference

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Leveraging the HapMap correlation structure in association studies

1 reference

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Whole-genome re-sequencing

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In silico method for inferring genotypes in pedigrees

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1 reference

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Additional SNPs and linkage-disequilibrium analyses are necessary for whole-genome association studies in humans

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Construction of multilocus genetic linkage maps in humans

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Conjuring SNPs to detect associations

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12 December 2020

based on heuristic

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10.1002/GEPI.20533

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PMC publication ID

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Consolidated OpenCitations Corpus – April 2017

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PubMed publication ID

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Consolidated OpenCitations Corpus – April 2017

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ResearchGate publication ID

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