(Q40603492)

6 October 2017

Next-generation genotype imputation service and methods (English)

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6 October 2017

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5

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22 September 2017

9

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22 September 2017

15

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22 September 2017

Lukas Forer

2

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Francesco Cucca

object named as

Francesco Cucca

17

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Michael Boehnke

19

object named as

Michael Boehnke

1 reference

6 October 2017

12

Dwight Stambolian

1 reference

6 October 2017

Christian Fuchsberger

21

object named as

Christian Fuchsberger

1 reference

6 October 2017

11

David Schlessinger

1 reference

6 October 2017

8

Emily Y Chew

1 reference

6 October 2017

10

Matt McGue

1 reference

6 October 2017

14

William G Iacono

1 reference

6 October 2017

20

Gonçalo R Abecasis

1 reference

6 October 2017

7

Scott I Vrieze

1 reference

6 October 2017

1

Sayantan Das

1 reference

6 October 2017

4

Carlo Sidore

1 reference

6 October 2017

16

Laura J Scott

1 reference

6 October 2017

Sebastian Schönherr

3

1 reference

6 October 2017

Alan Kwong

6

1 reference

6 October 2017

Po-Ru Loh

13

1 reference

6 October 2017

Florian Kronenberg

18

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6 October 2017

language of work or name

English

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publication date

29 August 2016

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6 October 2017

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6 October 2017

48

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6 October 2017

10

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6 October 2017

1284-1287

1 reference

https://scigraph.springernature.com/pub.10.1038/ng.3656

6 October 2017

0 references

cites work

A reference panel of 64,976 haplotypes for genotype imputation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5157836

Genotype Imputation with Millions of Reference Samples

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5157836

A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5157836

A global reference for human genetic variation

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5157836

Genome sequencing elucidates Sardinian genetic architecture and augments association analyses for lipid and blood inflammatory markers

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5157836

Large-scale whole-genome sequencing of the Icelandic population

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5157836

Identification of a large set of rare complete human knockouts

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5157836

Inactivating mutations in NPC1L1 and protection from coronary heart disease

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5157836

In search of rare variants: preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5157836

minimac2: faster genotype imputation

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5157836

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

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5157836

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

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5157836

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

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5157836

Cloudgene: a graphical execution platform for MapReduce programs on private and public clouds

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5157836

Phasing of many thousands of genotyped samples

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5157836

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

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5157836

Blockwise HMM computation for large-scale population genomic inference

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5157836

A systematic survey of loss-of-function variants in human protein-coding genes

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5157836

A linear complexity phasing method for thousands of genomes

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5157836

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

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5157836

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

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5157836

A map of human genome variation from population-scale sequencing

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5157836

Genotype imputation for genome-wide association studies

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5157836

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5157836

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

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5157836

Worldwide human relationships inferred from genome-wide patterns of variation

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5157836

A new multipoint method for genome-wide association studies by imputation of genotypes

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5157836

Possible ancestral structure in human populations

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5157836

Sequence variations in PCSK9, low LDL, and protection against coronary heart disease

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5157836

The International HapMap Project

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5157836

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

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5157836

Linkage disequilibrium in humans: models and data

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5157836

Efficient multipoint linkage analysis through reduction of inheritance space

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5157836

Improved whole-chromosome phasing for disease and population genetic studies

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5157836

MapReduce: Simplified Data Processing on Large Clusters

20 August 2018

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.3656

inferred from DOI database lookup

7 January 2021

based on heuristic

A Maximization Technique Occurring in the Statistical Analysis of Probabilistic Functions of Markov Chains

1 reference

Crossref

https://api.crossref.org/works/10.1038%2FNG.3656

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/NG.3656

1 reference

Dimensions Publication ID

6 October 2017

0 references

1 reference

6 October 2017

27571263

1 reference