Uncountable hours looking down a microscope at fish. Worth it. Can I call myself a scientist now? sciencedirect.com/science/articl…

Last week Dr Ali Kay 🧬📚🌳 and Dr Dale Maxwell from the Goriely group, in collaboration with Centre for Personalised Medicine, Oxford (+ bsky) went to Bartholomew School to run a workshop all about genomes, genetic variants and bioethics to celebrate British Science Week 2023. (1/2)

Come join us as a Postdoctoral Research Assistant in Molecular Genetics and be involved in cutting edge research investigating the origins of new mutations in the male germline 🧬 closing date to noon on 9/6. For more info see job description and/or drop us Anne Goriely an email!

Our very own Shiyan Tang presenting at #ETW23 - she’s discussing her project on ‘Exploiting multi-omics to map the fertility potential of prepubertal testicular tissues’ 🧬

Next up we have Dr Dale Maxwell presenting his work on ‘Intrinsic Factors Influencing Stem Cell Density’ at #ETW23!

Consider yourself as a Mick Jagger or Rrobert De Niro? Maybe reconsider. The Guardian speaks to our very own Anne Goriely about the potential genetic pitfalls of increasing paternal age. theguardian.com/science/2023/o…

Looking forward to hearing about the application of long read sequencing with Oxford Nanopore #WYMM #WYMMTour at the Oxford Natural History Museum

Fantastic time at the Mutations in Time and Space conference up in, surprisingly sunny, Edinburgh! Amazing talks and incredible science from everyone involved. We'll see you all again in 2 years time! #MITS24 #walkingbagofmutations

Our latest paper is out! [link: mdpi.com/2073-4409/13/9…] We've made an integrated single-cell atlas of human spermatogonial differentiation [link: trainingidn.shinyapps.io/hu_spermatogon…] using every publicly-available healthy adult human testis sample to date (Fig 1B). A thread (1/7).

After a few years of work, we have identified the first non RAS/MAPK pathway gene which is under 'selfish selection' in the male germline. With implications for those with Myhre Syndrome Foundation, our seminal work is published in AJHG