(Q36226921)

English

LDlink: a web-based application for exploring population-specific haplotype structure and linking correlated alleles of possible functional variants

scientific article

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Statements

scholarly article

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

LDlink: a web-based application for exploring population-specific haplotype structure and linking correlated alleles of possible functional variants (English)

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

web application

1 reference

based on heuristic

inferred from title

Mitchell Machiela

1

object named as

Mitchell J Machiela

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

Stephen Chanock

2

object named as

Stephen J Chanock

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

language of work or name

0 references

publication date

2 July 2015

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

31

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

21

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

3555-3557

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

describes a project that uses

1 reference

Europe PubMed Central

26 June 2022

https://europepmc.org/article/PMC/PMC4626747

based on heuristic

inferred from PubMed Central ID database lookup

The NHGRI GWAS Catalog, a curated resource of SNP-trait associations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4626747

1 October 2017

An integrated map of genetic variation from 1,092 human genomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4626747

1 October 2017

Annotation of functional variation in personal genomes using RegulomeDB

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4626747

1 October 2017

Tabix: fast retrieval of sequence features from generic TAB-delimited files

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4626747

1 October 2017

SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4626747

1 October 2017

Haploview: analysis and visualization of LD and haplotype maps

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4626747

1 October 2017

Identifiers

10.1093/BIOINFORMATICS/BTV402

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

DBLP publication ID

journals/bioinformatics/MachielaC15

1 reference

DBLP Dataset 2021-01-02

28 January 2021

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

12 August 2017

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