(Q34262786)

1 August 2017

title

Association testing for next-generation sequencing data using score statistics (English)

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1 August 2017

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Thorfinn Korneliussen

series ordinal

2

object named as

Thorfinn Sand Korneliussen

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Line Skotte

object named as

Line Skotte

series ordinal

1

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Anders Albrechtsen

object named as

Anders Albrechtsen

series ordinal

3

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publication date

8 May 2012

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1 August 2017

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1 August 2017

volume

36

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1 August 2017

issue

5

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1 August 2017

page(s)

430-437

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A map of human genome variation from population-scale sequencing

1 August 2017

cites work

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https://api.crossref.org/works/10.1002%2FGEPI.21636

7 January 2021

Missing data imputation and haplotype phase inference for genome-wide association studies

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https://api.crossref.org/works/10.1002%2FGEPI.21636

7 January 2021

A second generation human haplotype map of over 3.1 million SNPs

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.21636

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.21636

7 January 2021

Design of association studies with pooled or un-pooled next-generation sequencing data

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.21636

7 January 2021

Estimation of allele frequency and association mapping using next-generation sequencing data

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.21636

7 January 2021

Fast and accurate short read alignment with Burrows-Wheeler transform

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.21636

7 January 2021

Mapping short DNA sequencing reads and calling variants using mapping quality scores

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.21636

7 January 2021

The Sequence Alignment/Map format and SAMtools

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https://api.crossref.org/works/10.1002%2FGEPI.21636

7 January 2021

SNP detection for massively parallel whole-genome resequencing

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.21636

7 January 2021

Resequencing of 200 human exomes identifies an excess of low-frequency non-synonymous coding variants

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.21636

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.21636

7 January 2021

SeqEM: an adaptive genotype-calling approach for next-generation sequencing studies

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.21636

7 January 2021

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.21636

7 January 2021

Exome sequencing identifies the cause of a mendelian disorder

1 reference

https://api.crossref.org/works/10.1002%2FGEPI.21636

7 January 2021

Score tests for association between traits and haplotypes when linkage phase is ambiguous

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https://api.crossref.org/works/10.1002%2FGEPI.21636

7 January 2021

Identifiers

DOI

10.1002/GEPI.21636

1 reference

1 August 2017

1 reference