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Accurate, scalable and integrative haplotype estimation

Nature communications, 2019-11, Vol.10 (1), p.5436-10, Article 5436

2019

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Improved whole-chromosome phasing for disease and population genetic studies

Nature methods, 2013-01, Vol.10 (1), p.5-6

2013

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A linear complexity phasing method for thousands of genomes

Nature methods, 2012-02, Vol.9 (2), p.179-181

2012

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Genotype imputation using the Positional Burrows Wheeler Transform

PLoS genetics, 2020-11, Vol.16 (11), p.e1009049-e1009049

2020

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Are drug targets with genetic support twice as likely to be approved? Revised estimates of the impact of genetic support for drug mechanisms on the probability of drug approval

PLoS genetics, 2019-12, Vol.15 (12), p.e1008489-e1008489

2019

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Computationally efficient whole-genome regression for quantitative and binary traits

Nature genetics, 2021-07, Vol.53 (7), p.1097-1103

2021

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HAPGEN2: simulation of multiple disease SNPs

Bioinformatics, 2011-08, Vol.27 (16), p.2304-2305

2011

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

Nature genetics, 2007-07, Vol.39 (7), p.906-913

2007

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

Nature genetics, 2012-08, Vol.44 (8), p.955-959

2012

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

PLoS genetics, 2009-06, Vol.5 (6), p.e1000529-e1000529

2009

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Comparison of phasing strategies for whole human genomes

PLoS genetics, 2018-04, Vol.14 (4), p.e1007308-e1007308

2018

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A reference panel of 64,976 haplotypes for genotype imputation

Nature genetics, 2016-10, Vol.48 (10), p.1279-1283

2016

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Handedness, language areas and neuropsychiatric diseases: insights from brain imaging and genetics

Brain (London, England : 1878), 2019-10, Vol.142 (10), p.2938-2947

2019

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Statistical correction of the Winner's Curse explains replication variability in quantitative trait genome-wide association studies

PLoS genetics, 2017-07, Vol.13 (7), p.e1006916-e1006916

2017

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A Simple Model-Based Approach to Inferring and Visualizing Cancer Mutation Signatures

PLoS genetics, 2015-12, Vol.11 (12), p.e1005657-e1005657

2015

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Crossover interference and sex-specific genetic maps shape identical by descent sharing in close relatives

PLoS genetics, 2019-12, Vol.15 (12), p.e1007979-e1007979

2019

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Designing genome-wide association studies: sample size, power, imputation, and the choice of genotyping chip

PLoS genetics, 2009-05, Vol.5 (5), p.e1000477-e1000477

2009

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

Bioinformatics, 2013-01, Vol.29 (1), p.84-91

2013

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A general approach for haplotype phasing across the full spectrum of relatedness

PLoS genetics, 2014-04, Vol.10 (4), p.e1004234-e1004234

2014

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Meta-GWAS Accuracy and Power (MetaGAP) Calculator Shows that Hiding Heritability Is Partially Due to Imperfect Genetic Correlations across Studies

PLoS genetics, 2017-01, Vol.13 (1), p.e1006495-e1006495

2017

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An imputation platform to enhance integration of rice genetic resources

Nature communications, 2018-08, Vol.9 (1), p.3519-10, Article 3519

2018

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Imputed genomes and haplotype-based analyses of the Picts of early medieval Scotland reveal fine-scale relatedness between Iron Age, early medieval and the modern people of the UK

PLoS genetics, 2023-04, Vol.19 (4), p.e1010360-e1010360

2023

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Unified single-cell analysis of testis gene regulation and pathology in five mouse strains

eLife, 2019-06, Vol.8

2019

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Genotype imputation for genome-wide association studies

Nature reviews. Genetics, 2010-07, Vol.11 (7), p.499-511

2010

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Increasing calling accuracy, coverage, and read-depth in sequence data by the use of haplotype blocks

PLoS genetics, 2021-12, Vol.17 (12), p.e1009944-e1009944

2021

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Accurate, scalable and integrative haplotype estimation

Improved whole-chromosome phasing for disease and population genetic studies

A linear complexity phasing method for thousands of genomes

Genotype imputation using the Positional Burrows Wheeler Transform

Are drug targets with genetic support twice as likely to be approved? Revised estimates of the impact of genetic support for drug mechanisms on the probability of drug approval

Computationally efficient whole-genome regression for quantitative and binary traits

HAPGEN2: simulation of multiple disease SNPs

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

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

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

Comparison of phasing strategies for whole human genomes

A reference panel of 64,976 haplotypes for genotype imputation

Handedness, language areas and neuropsychiatric diseases: insights from brain imaging and genetics

Statistical correction of the Winner's Curse explains replication variability in quantitative trait genome-wide association studies

A Simple Model-Based Approach to Inferring and Visualizing Cancer Mutation Signatures

Crossover interference and sex-specific genetic maps shape identical by descent sharing in close relatives

Designing genome-wide association studies: sample size, power, imputation, and the choice of genotyping chip

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

A general approach for haplotype phasing across the full spectrum of relatedness

Meta-GWAS Accuracy and Power (MetaGAP) Calculator Shows that Hiding Heritability Is Partially Due to Imperfect Genetic Correlations across Studies

An imputation platform to enhance integration of rice genetic resources

Imputed genomes and haplotype-based analyses of the Picts of early medieval Scotland reveal fine-scale relatedness between Iron Age, early medieval and the modern people of the UK

Unified single-cell analysis of testis gene regulation and pathology in five mouse strains

Genotype imputation for genome-wide association studies

Increasing calling accuracy, coverage, and read-depth in sequence data by the use of haplotype blocks

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