Haplotype inference in random population samples. (Q37363777)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12386835%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

title

Haplotype inference in random population samples (English)

1 reference

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14 December 2019

1

1 reference

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14 December 2019

3

Michael E Zwick

1 reference

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14 December 2019

author name string

David J Cutler

series ordinal

2

1 reference

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14 December 2019

Aravinda Chakravarti

series ordinal

4

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14 December 2019

language of work or name

English

0 references

publication date

17 October 2002

1 reference

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American Journal of Human Genetics

14 December 2019

published in

1 reference

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14 December 2019

volume

71

1 reference

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14 December 2019

issue

5

1 reference

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14 December 2019

page(s)

1129-1137

1 reference

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Bayesian haplotype inference for multiple linked single-nucleotide polymorphisms

14 December 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=385088

High-throughput variation detection and genotyping using microarrays

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=385088

Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=385088

Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=385088

A chronology of fine-scale gene mapping by linkage disequilibrium

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=385088

A New Statistical Method for Haplotype Reconstruction from Population Data

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=385088

A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=385088

Accuracy of haplotype frequency estimation for biallelic loci, via the expectation-maximization algorithm for unphased diploid genotype data

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=385088

A DNA polymorphism discovery resource for research on human genetic variation

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=385088

The future of genetic studies of complex human diseases

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=385088

Identity-by-descent and association mapping of a recessive gene for Hirschsprung disease on human chromosome 13q22

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=385088

Maximum-likelihood estimation of molecular haplotype frequencies in a diploid population

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=385088

On measures of gametic disequilibrium

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=385088

Inference of haplotypes from PCR-amplified samples of diploid populations

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=385088

Monoallelic mutation analysis (MAMA) for identifying germline mutations

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=385088

Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=385088

High-resolution haplotype structure in the human genome

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=385088

Comparisons of two methods for haplotype reconstruction and haplotype frequency estimation from population data

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=385088

Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease

2 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=385088

Experimentally-derived haplotypes substantially increase the efficiency of linkage disequilibrium studies

3 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/12386835

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1086/344347

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12386835%20AND%20SRC:MED&resulttype=core&format=json

release_ae43qre6jfbnrlv5akqa444wmu

14 December 2019

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/ae43qre6jfbnrlv5akqa444wmu

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12386835%20AND%20SRC:MED&resulttype=core&format=json

14 December 2019

PubMed publication ID

12386835

1 reference