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Publications

Publisher Correction: Inferring whole-genome histories in large population datasets

Kelleher J. et al, (2019), Nature Genetics, 51, 1660 - 1660

Inferring whole-genome histories in large population datasets

Kelleher J. et al, (2019), Nature Genetics, 51, 1330 - 1338

Identification of host-pathogen-disease relationships using a scalable Multiplex Serology platform in UK Biobank

Mentzer AJ. et al, (2019)

Detection of simple and complex de novo mutations without, with, or with multiple reference sequences

Garimella KV. et al, (2019)

Mapping the drivers of within-host pathogen evolution using massive data sets.

Palmer DS. et al, (2019), Nature communications, 10

A genetics-led approach defines the drug target landscape of 30 immune-related traits

Fang H. et al, (2019), Nature Genetics, 51, 1082 - 1091

Coupling Wright-Fisher and coalescent dynamics for realistic simulation of population-scale datasets

Nelson D. et al, (2019)

HLA*LA - HLA typing from linearly projected graph alignments.

Dilthey AT. et al, (2019), Bioinformatics

Bayesian meta-analysis across genome-wide association studies of diverse phenotypes.

Trochet H. et al, (2019), Genet Epidemiol

Ultrafast search of all deposited bacterial and viral genomic data

Bradley P. et al, (2019), Nature Biotechnology, 37, 152 - 159

Genomic analysis of Plasmodium vivax in southern Ethiopia reveals selective pressures in multiple parasite mechanisms.

Auburn S. et al, (2019), J Infect Dis

Low-Bias RNA Sequencing of the HIV-2 Genome from Blood Plasma.

James KL. et al, (2019), J Virol, 93

Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

Flannick J. et al, (2018), Scientific Data, 5

Inferring the ancestry of everyone

Kelleher J. et al, (2018)

Selfish mutations dysregulating RAS-MAPK signaling are pervasive in aged human testes.

Maher GJ. et al, (2018), Genome Res

LOW-BIAS RNA SEQUENCING OF THE HIV-2 GENOME FROM BLOOD PLASMA.

James KL. et al, (2018), J Virol

The UK Biobank resource with deep phenotyping and genomic data.

Bycroft C. et al, (2018), Nature, 562, 203 - 209

Dating genomic variants and shared ancestry in population-scale sequencing data

Albers P. and McVean G., (2018)

Systematic classification of shared components of genetic risk for common human diseases

Cortes A. et al, (2018)

Graphical Model Selection for Gaussian Conditional Random Fields in the Presence of Latent Variables

Frot B. et al, (2018), Journal of the American Statistical Association, 1 - 12

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