Author

Gerton Lunter

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Bioinformatics· 1 Evolutionary Biology· 1 Genomics· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Approach:statistical model· 3 Research Focus:variant calling· 2 Approach:deep learning· 1 Organism:human· 1 Research Focus:phylogenetics / evolution· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Ann Strydom· 1 shared Anthony Renwick· 1 shared Elise RuarkiD· 1 shared Emma Ramsay· 1 shared Kenneth Hoehn· 1 shared Márton Münz· 1 shared Matthew Clarke· 1 shared Nazneen RahmaniD· 1 shared

Activity by Year

2015-2016 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

1 shared paperGenomics

Ann Strydom

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

A phylogenetic codon substitution model for antibody lineages

Kenneth Hoehn, Gerton Lunter, Oliver Pybus

This paper develops a phylogenetic substitution model that accounts for hotspot motifs in antibody lineage evolution, showing improved fit and reduced bias in parameter estimation.

bioRxiv · May 26, 2016Evolutionary Biology

Fast haplotype matching in very large cohorts using the Li and Stephens model

Gerton Lunter

This paper introduces an exact algorithm for haplotype matching in large cohorts using the Li and Stephens model, achieving runtime independent of cohort size.

bioRxiv · Apr 12, 2016 · PreprintBioinformatics

CSN and CAVA: variant annotation tools for rapid, robust next-generation sequencing analysis in the clinic

Márton Münz, Elise Ruark, Anthony Renwick, Emma Ramsay, Matthew Clarke, Shazia Mahamdallie, Victoria Cloke, Sheila Seal, Ann Strydom, Gerton Lunter, Nazneen Rahman

This paper introduces CSN and CAVA, tools for standardized, rapid variant annotation of NGS data, showing high accuracy and clinical relevance in BRCA1/BRCA2 analysis.

bioRxiv · Mar 21, 2015Genomics