Colin Semple

@csemple.bsky.social

Genomics, bioinformatics; attempting to say useful things about cancer and evolution. Institute of Genetics and Cancer, University of Edinburgh https://institute-genetics-cancer.ed.ac.uk https://semplelab.com

New preprint from the lab! Profiling triple negative breast cancer samples over time, we looked at tumour genome responses to treatment. We reveal major roles for whole genome duplication (WGD) as these tumours evolve; with WGD seen in many pre-treatment samples, but also re-emerging at recurrence.

bioRxiv Genomics@biorxiv-genomic.bsky.social · 9mo ago

Frequent Whole-Genome Duplication Events Drive the Genomic Evolution of Triple-Negative Breast Cancer During Neoadjuvant Chemotherapy https://www.biorxiv.org/content/10.1101/2025.11.17.688693v1

tl;dr — this EO co-opts the language of open science to implement a system of political control wherein presidential appointees are given broad latitude to designate any number of reasonable scientific activities and inferences as scientific misconduct, and to penalize those involved accordingly.

Restoring Gold Standard Science

By the authority vested in me as President by the Constitution and the laws of the United States of America, including section 7301 of title 5, United

whitehouse.gov

Watching the US take a wrecking ball to science 💔 🤯 Reminder of the importance of doing science in the open. Put data, software, resources in public domain, where no single govt can erase them. This is our collective knowledge. Distributed data systems are essential. www.nature.com/articles/s41...

Genomic data sharing: you don’t know what you’ve got (till it’s gone) - Nature Reviews Genetics

Reflecting on the core values of early data sharing agreements, the Bermuda Principles and the Fort Lauderdale Agreement, Kathryn E. Holt and Michael Inouye emphasize the need to reaffirm our commitme...

nature.com

We are happy to announce the release of a new #nf-core workflow -- #oncoanalyser performs an exhaustive analysis of single-patient cancer sequencing data using methods developed by the Hartwig Medical Foundation Australia. (1/5)