(Q41530610)

2 October 2017

title

Population-specific genotype imputations using minimac or IMPUTE2. (English)

1 reference

2 October 2017

3

1 reference

2 October 2017

12

1 reference

2 October 2017

Cornelia M. van Duijn

11

object named as

Cornelia M van Duijn

0 references

Cisca Wijmenga

8

object named as

Cisca Wijmenga

0 references

Morris A Swertz

9

object named as

Morris A Swertz

1 reference

2 October 2017

10

Dorret I Boomsma

1 reference

2 October 2017

13

Jouke Jan Hottenga

1 reference

2 October 2017

6

P Eline Slagboom

1 reference

2 October 2017

author name string

Elisabeth M van Leeuwen

1

1 reference

2 October 2017

Alexandros Kanterakis

2

1 reference

2 October 2017

Mathijs V Kattenberg

4

1 reference

2 October 2017

Genome of the Netherlands Consortium

5

1 reference

2 October 2017

Paul I W de Bakker

7

1 reference

2 October 2017

publication date

30 July 2015

1 reference

2 October 2017

1 reference

2 October 2017

volume

10

1 reference

2 October 2017

issue

9

1 reference

2 October 2017

page(s)

1285-1296

1 reference

Integrating common and rare genetic variation in diverse human populations

2 October 2017

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2015.077

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2015.077

The Genome of the Netherlands: design, and project goals

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2015.077

Improved imputation quality of low-frequency and rare variants in European samples using the 'Genome of The Netherlands'.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2015.077

Whole-genome sequence variation, population structure and demographic history of the Dutch population

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2015.077

Genotype imputation for genome-wide association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2015.077

Data quality control in genetic case-control association studies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2015.077

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2015.077

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2015.077

Imputation and quality control steps for combining multiple genome-wide datasets

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2015.077

Quality control and conduct of genome-wide association meta-analyses

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2015.077

Fast and accurate genotype imputation in genome-wide association studies through pre-phasing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2015.077

Genome of The Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2015.077

Imputation of low-frequency variants using the HapMap3 benefits from large, diverse reference sets

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2015.077

Rare variant genotype imputation with thousands of study-specific whole-genome sequences: implications for cost-effective study designs

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2015.077

Haplotype phasing: existing methods and new developments

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2015.077

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2015.077

Improved whole-chromosome phasing for disease and population genetic studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2015.077

The variant call format and VCFtools

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2015.077

fcGENE: a versatile tool for processing and transforming SNP datasets

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2015.077

Is 'forward' the same as 'plus'?…and other adventures in SNP allele nomenclature

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2015.077

Genotype harmonizer: automatic strand alignment and format conversion for genotype data integration

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2015.077

GACT: a Genome build and Allele definition Conversion Tool for SNP imputation and meta-analysis in genetic association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2015.077

Practical aspects of imputation-driven meta-analysis of genome-wide association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2015.077

Improved imputation of common and uncommon SNPs with a new reference set.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2015.077

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2015.077

The human genome browser at UCSC

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNPROT.2015.077

The effect of reference panels and software tools on genotype imputation

31 March 2020

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26226460

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NPROT.2015.077

1 reference

2 October 2017

1 reference