Greg S Elgar
6PUBLICATIONS
91CO-AUTHORS
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Publications (6)
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|May 28, 2025
SAVANA: reliable analysis of somatic structural variants and copy number aberrations using long-read sequencing.Hillary Elrick, Carolin M Sauer, Jose Espejo Valle-Inclan
|Oct 31, 2024
Large-Scale Pharmacogenomics Analysis of Patients With Cancer Within the 100,000 Genomes Project Combining Whole-Genome Sequencing and Medical Records to Inform Clinical Practice.Ivone U S Leong, Claudia P Cabrera, Valentina Cipriani
|Sep 04, 2024
Large-scale analysis of whole genome sequencing data from formalin-fixed paraffin-embedded cancer specimens demonstrates preservation of clinical utility.Shadi Basyuni, Laura Heskin, Andrea Degasperi
|Nov 18, 2023
Long read sequencing characterises a novel structural variant, revealing underactive AKR1C1 with overactive AKR1C2 as a possible cause of severe chronic fatigue.Julia Oakley, Martin Hill, Adam Giess
|Oct 05, 2022
Nuclear-embedded mitochondrial DNA sequences in 66,083 human genomes.Wei Wei, Katherine R Schon, Greg Elgar
|Mar 07, 2022
Whole-genome sequencing reveals host factors underlying critical COVID-19.Athanasios Kousathanas, Erola Pairo-Castineira, Konrad Rawlik
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Frequent Collaborators
3 joint publications
Mark J Caulfield
2 joint publications
Alona Sosinsky
2 joint publications
Mélanie Tanguy
2 joint publications
Susan Walker
2 joint publications
Marc Tischkowitz
2 joint publications
Matthew A Brown
2 joint publications
Loukas Moutsianas
1 joint publications
Erola Pairo-Castineira
1 joint publications
Tomas Malinauskas
1 joint publications
Yang Wu
