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Mapping and phasing of structural variation in patient genomes using nanopore sequencing

Nature communications, 2017-11, Vol.8 (1), p.1326-13, Article 1326

2017

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Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses

Nature genetics, 2021-08, Vol.53 (8), p.1260-1269

2021

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Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes

Nature genetics, 2018-04, Vol.50 (4), p.559-571

2018

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

Genome Research, 2008-11, Vol.18 (11), p.1851-1858

2008

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Analysis of 589,306 genomes identifies individuals resilient to severe Mendelian childhood diseases

Nature biotechnology, 2016-05, Vol.34 (5), p.531-538

2016

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The statistics of bulk segregant analysis using next generation sequencing

PLoS computational biology, 2011-11, Vol.7 (11), p.e1002255-e1002255

2011

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Detecting epistasis with the marginal epistasis test in genetic mapping studies of quantitative traits

PLoS genetics, 2017-07, Vol.13 (7), p.e1006869-e1006869

2017

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A survey of error-correction methods for next-generation sequencing

Briefings in bioinformatics, 2013-01, Vol.14 (1), p.56-66

2013

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Genetic association mapping and genome organization of maize

Current opinion in biotechnology, 2006-04, Vol.17 (2), p.155-160

2006

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Quantifying the mapping precision of genome-wide association studies using whole-genome sequencing data

Genome Biology, 2017-05, Vol.18 (1), p.86-86, Article 86

2017

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A barrier nucleosome model for statistical positioning of nucleosomes throughout the yeast genome

Genome Research, 2008-07, Vol.18 (7), p.1073-1083

2008

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Statistical challenges associated with detecting copy number variations with next-generation sequencing

Bioinformatics, 2012-11, Vol.28 (21), p.2711-2718

2012

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Optimizing expression quantitative trait locus mapping workflows for single-cell studies

Genome Biology, 2021-06, Vol.22 (1), p.188-188, Article 188

2021

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Efficient and accurate construction of genetic linkage maps from the minimum spanning tree of a graph

PLoS genetics, 2008-10, Vol.4 (10), p.e1000212-e1000212

2008

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High-resolution mapping of expression-QTLs yields insight into human gene regulation

PLoS genetics, 2008-10, Vol.4 (10), p.e1000214-e1000214

2008

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Prophages are associated with extensive CRISPR-Cas auto-immunity

Nucleic acids research, 2020-12, Vol.48 (21), p.12074-12084

2020

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Enredo and Pecan: genome-wide mammalian consistency-based multiple alignment with paralogs

Genome Research, 2008-11, Vol.18 (11), p.1814-1828

2008

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Bayesian LASSO for Quantitative Trait Loci Mapping

Genetics (Austin), 2008-06, Vol.179 (2), p.1045-1055

2008

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Identification of four novel QTL linked to the metabolic syndrome in the Berlin Fat Mouse

International Journal of Obesity, 2022-02, Vol.46 (2), p.307-315

2022

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Powerful gene set analysis in GWAS with the Generalized Berk-Jones statistic

PLoS genetics, 2019-03, Vol.15 (3), p.e1007530

2019

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A second-generation combined linkage physical map of the human genome

Genome Research, 2007-12, Vol.17 (12), p.1783-1786

2007

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Cross-Disorder Genomewide Analysis of Schizophrenia, Bipolar Disorder, and Depression

The American journal of psychiatry, 2010-10, Vol.167 (10), p.1254-1263

2010

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Probabilistic Estimation of Identity by Descent Segment Endpoints and Detection of Recent Selection

American journal of human genetics, 2020-11, Vol.107 (5), p.895-910

2020

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Fine human genetic map based on UK10K data set

Human genetics, 2022-02, Vol.141 (2), p.273-281

2022

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Identification of Restless Legs Syndrome Genes by Mutational Load Analysis

Annals of neurology, 2020-02, Vol.87 (2), p.184-193

2020

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Mapping and phasing of structural variation in patient genomes using nanopore sequencing

Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses

Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes

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

Analysis of 589,306 genomes identifies individuals resilient to severe Mendelian childhood diseases

The statistics of bulk segregant analysis using next generation sequencing

Detecting epistasis with the marginal epistasis test in genetic mapping studies of quantitative traits

A survey of error-correction methods for next-generation sequencing

Genetic association mapping and genome organization of maize

Quantifying the mapping precision of genome-wide association studies using whole-genome sequencing data

A barrier nucleosome model for statistical positioning of nucleosomes throughout the yeast genome

Statistical challenges associated with detecting copy number variations with next-generation sequencing

Optimizing expression quantitative trait locus mapping workflows for single-cell studies

Efficient and accurate construction of genetic linkage maps from the minimum spanning tree of a graph

High-resolution mapping of expression-QTLs yields insight into human gene regulation

Prophages are associated with extensive CRISPR-Cas auto-immunity

Enredo and Pecan: genome-wide mammalian consistency-based multiple alignment with paralogs

Bayesian LASSO for Quantitative Trait Loci Mapping

Identification of four novel QTL linked to the metabolic syndrome in the Berlin Fat Mouse

Powerful gene set analysis in GWAS with the Generalized Berk-Jones statistic

A second-generation combined linkage physical map of the human genome

Cross-Disorder Genomewide Analysis of Schizophrenia, Bipolar Disorder, and Depression

Probabilistic Estimation of Identity by Descent Segment Endpoints and Detection of Recent Selection

Fine human genetic map based on UK10K data set

Identification of Restless Legs Syndrome Genes by Mutational Load Analysis

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