(Q43495071)

24 November 2017

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

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24 November 2017

Androniki Menelaou

1

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24 November 2017

Jonathan Marchini

series ordinal

2

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24 November 2017

language of work or name

English

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publication date

23 October 2012

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24 November 2017

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24 November 2017

29

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24 November 2017

1

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24 November 2017

84-91

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describes a project that uses

24 November 2017

massive parallel sequencing

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based on heuristic

inferred from title

cites work

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

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTS632

Detecting disease associations due to linkage disequilibrium using haplotype tags: a class of tests and the determinants of statistical power

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTS632

Using environmental correlations to identify loci underlying local adaptation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTS632

A linear complexity phasing method for thousands of genomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTS632

Genotype imputation with thousands of genomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTS632

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/10.1093%2FBIOINFORMATICS%2FBTS632

Integrating common and rare genetic variation in diverse human populations

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTS632

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTS632

Detection of sharing by descent, long-range phasing and haplotype imputation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTS632

SNP detection and genotyping from low-coverage sequencing data on multiple diploid samples

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTS632

The Sequence Alignment/Map format and SAMtools

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTS632

Haplotype-based linkage disequilibrium mapping via direct data mining

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTS632

Low-coverage sequencing: implications for design of complex trait association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTS632

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTS632

Finding the missing heritability of complex diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTS632

Genotype imputation for genome-wide association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTS632

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTS632

Genome-wide association studies for complex traits: consensus, uncertainty and challenges

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTS632

Joint genotype calling with array and sequence data

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTS632

Extremely low-coverage sequencing and imputation increases power for genome-wide association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTS632

A comparison of bayesian methods for haplotype reconstruction from population genotype data

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTS632

USING LINEAR PREDICTORS TO IMPUTE ALLELE FREQUENCIES FROM SUMMARY OR POOLED GENOTYPE DATA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTS632

Assessing population differentiation and isolation from single-nucleotide polymorphism data

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBIOINFORMATICS%2FBTS632

10.1093/BIOINFORMATICS/BTS632

21 January 2018

Identifiers

DOI

1 reference

journals/bioinformatics/MenelaouM13

24 November 2017

1 reference

DBLP Dataset 2021-01-02

28 January 2021

1 reference