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Recent publications published by researchers at the MRC WIMM.

Neuropeptide S receptor 1 is a nonhormonal treatment target in endometriosis.

Journal article

Tapmeier TT. et al, (2021), Sci Transl Med, 13

Multi Locus View: an extensible web-based tool for the analysis of genomic data.

Journal article

Sergeant MJ. et al, (2021), Commun Biol, 4

A unified haplotype-based method for accurate and comprehensive variant calling.

Journal article

Cooke DP. et al, (2021), Nat Biotechnol

DeepC: predicting 3D genome folding using megabase-scale transfer learning.

Journal article

Schwessinger R. et al, (2020), Nat Methods, 17, 1118 - 1124

Inferring B cell specificity for vaccines using a Bayesian mixture model.

Journal article

Fowler A. et al, (2020), BMC Genomics, 21

Repertoire-wide phylogenetic models of B cell molecular evolution reveal evolutionary signatures of aging and vaccination.

Journal article

Hoehn KB. et al, (2019), Proc Natl Acad Sci U S A, 116, 22664 - 22672

An equivariant Bayesian convolutional network predicts recombination hotspots and accurately resolves binding motifs.

Journal article

Brown RC. and Lunter G., (2019), Bioinformatics, 35, 2177 - 2184

Sequencing of human genomes with nanopore technology.

Journal article

Bowden R. et al, (2019), Nat Commun, 10

Haplotype matching in large cohorts using the Li and Stephens model.

Journal article

Lunter G., (2019), Bioinformatics, 35, 798 - 806

Efficient inference in state-space models through adaptive learning in online Monte Carlo expectation maximization

Journal article

Henderson D. and Lunter G., (2019), Computational Statistics

Non-Mendelian Causes of Temporal Lobe Epilepsy

Conference paper

Krestel H. et al, (2018), EPILEPSIA, 59, S316 - S316

A high throughput screen for active human transposable elements.

Journal article

Kvikstad EM. et al, (2018), BMC Genomics, 19

A Phylogenetic Codon Substitution Model for Antibody Lineages.

Journal article

Hoehn KB. et al, (2017), Genetics, 206, 417 - 427

Accurate clinical detection of exon copy number variants in a targeted NGS panel using DECoN.

Journal article

Fowler A. et al, (2016), Wellcome Open Res, 1

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