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Exploring rare cancer mutational signatures with whole genome sequencing

Written by Liam Little, Science Writer A new study, published in Science, has used whole genome sequencing (WGS) to explore […]

Genomics week in brief: Week ending 13th August

Check out the latest Genomics Week in Brief – full of intriguing news and research from the genomics space! Top […]

A Spotlight On: Spatial Transcriptomics – Jeffrey Moffitt, Assistant Professor, Harvard Medical School

Jeffrey Moffitt is an Assistant Professor at Boston Children’s Hospital and Harvard Medical School. His lab uses state-of-the-art spatially resolved […]

Genomics week in brief: Week ending 6th August

Check out the latest Genomics Week in Brief – full of intriguing news and research from the genomics space! Top […]

World of Genomics: Morocco

The Kingdom of Morocco, bordering the Sahara Desert and the strait of Gibraltar, is best known for its mountain ranges, […]

A Spotlight On: Variants of uncertain significance – Kimberly Gilmour

Kimberly Gilmour is Director of Laboratory Medicine at Great Ormond Street Hospital for Children. She utilises next generation sequencing and […]

A Spotlight On: Genomic drivers of heart attacks – Akl Fahed

Akl Fahed, MD, MPH is a physician, scientist, and innovator. He works at Mass General Hospital, the Broad Institute of […]

5 recommendations for improving rigour and reproducibility in single-cell genomics

An opinion article by Professor Gregory Gibson, Georgia Institute of Technology and director of the Center for Integrative Genomics, offers […]

Genomics in Drug Discovery ONLINE – May 2022

Join us for Genomics in Drug Discovery ONLINE, a unique 3-part webinar series, where we explore the role of genetics […]

Researchers Identify Jumping “Junk” DNA as a Novel Cause of Paediatric Brain Cancer

Written by Bethany Hoernfeldt, Science Writer  Researchers at St. Jude Children’s Hospital have discovered the first causal link between “jumping” […]