(Q34461378)

2 August 2017

Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel (English)

1 reference

2 August 2017

3

1000 Genomes Project Consortium

1 reference

2 August 2017

2

Jonathan Marchini

1 reference

ORCID Public Data File 2021

2 August 2017

1 reference

Andrew G. Clark

1 reference

ORCID Public Data File 2021

Andrea Angius

1 reference

ORCID Public Data File 2021

author name string

Olivier Delaneau

series ordinal

1

1 reference

PubMed ID

25653097

2 August 2017

1000 Genomes Project Consortium

series ordinal

4

1 reference

PubMed ID

25653097

2 August 2017

language of work or name

English

0 references

publication date

13 June 2014

1 reference

2 August 2017

Nature Communications

1 reference

2 August 2017

5

1 reference

2 August 2017

3934

1 reference

https://scigraph.springernature.com/pub.10.1038/ncomms4934

2 August 2017

0 references

cites work

Haplotype estimation using sequencing reads

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4338501

Joint haplotype phasing and genotype calling of multiple individuals using haplotype informative reads

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4338501

Leveraging reads that span multiple single nucleotide polymorphisms for haplotype inference from sequencing data

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4338501

An integrative variant analysis pipeline for accurate genotype/haplotype inference in population NGS data

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4338501

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4338501

Genotype imputation with thousands of genomes

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4338501

A linear complexity phasing method for thousands of genomes

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4338501

A statistical framework for SNP calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4338501

Genotype and SNP calling from next-generation sequencing data

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4338501

A framework for variation discovery and genotyping using next-generation DNA sequencing data

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4338501

Discovery and genotyping of genome structural polymorphism by sequencing on a population scale

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4338501

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4338501

Genotype imputation for genome-wide association studies

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4338501

A flexible and accurate genotype imputation method for the next generation of genome-wide association studies

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4338501

A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4338501

Improved whole-chromosome phasing for disease and population genetic studies

6 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNCOMMS4934

Genotype calling and phasing using next-generation sequencing reads and a haplotype scaffold

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNCOMMS4934

21 January 2018

Identifiers

DOI

10.1038/NCOMMS4934

1 reference

Dimensions Publication ID

2 August 2017

0 references

0 references

1 reference

2 August 2017

1 reference

PubMed ID

25653097