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Great preprint about foetal haematopoiesis characterized by single-cell RNA and ATAC is out! biorxiv.org/content/10.110… Congratz to all the authors especially Andrea Tangherloni and Anna Maria Ranzoni who were driving this project!

Happy to be part of this great work on scRNA and scATAC in early HSC differentiation from the Ana Cvejic group at Wellcome Sanger Institute lead by @annaranzoni and Andrea Tangherloni - scATAC analysis from Ivan Berest

Our new preprint on lineage tracing of human embryonic development and foetal haematopoiesis using somatic mutations is out on BiorXiv! This work is a collaboration between the Cvejic group Cambridge Stem Cell Institute & Michael Spencer Chapman & the Campbell group Wellcome Sanger Institute

Dear epigenetic enthusiasts, This year, the Cambridge Epigenetics Summer Symposium is going virtual (24/07 2-5pm). Great keynote speaker: Geneviève Almouzni Talks will be selected from abstracts. Please register/submit abstracts @ abcam.com/events/cambrid… CambridgeEpigenetics epigenetics_papers

Single-cell analysis of gastric #cancer samples tracks the cell of origin of #metastatic lesions and identifies an independent prognostic signature of the clinical outcome. Linghua Wang, MD, PhD MD Anderson Cancer Center #EndCancer #gastriccancer #scRNAseq go.nature.com/3hIyAw6

Genomic research has evolved from seeking to understand the fundamentals of the human genetic code to examining the ways in which this code varies among people, and then applying this knowledge to interventions that are tailored to target the underlying causes of disease.

We are VERY excited about the future of genomics, so we are starting a seminar series to keep talking about it! Speakers will present their research and answer your questions about how their work fits into our Bold Predictions for the future of genomics. bit.ly/3oFmCGp

Analysis of 10,900 whole-exome sequences linked to electronic health care records in the Penn Medicine Biobank enabled an exome-wide study of the phenotypic effects of rare loss-of-function gene variants Joe Park, MD, PhD Daniel Rader Dr. Marylyn D. Ritchie, PhD go.nature.com/2N1xEaV

"Tree thinking" meets #CellBiology: In a new #SciMagReview, researchers evaluate ideas taken from phylodynamics of infectious disease & show how similar tree-building techniques can be applied to monitoring changes in somatic cell lineages. Learn more: ($) fcld.ly/gw8dox6

After nearly five years of work from researchers including Amit V. Khera, a Broad discovery — polygenic scoring for genetic risk assessment for a common disease — has found its way into the clinic...an important step for genomic medicine. broad.io/polygenicscori…

Our #genetics and #genetherapy editor Anna Maria Ranzoni is attending #VKSOmicEngineering21 this week. Get in touch if you'd like to chat and learn more about Nature Medicine! Keystone Symposia #eSymposia

Our #genetics and #genetherapy editor Anna Maria Ranzoni is attending the CSHL Nucleic Acid Therapies meeting #cshlNAT this week. Get in touch if you'd like to chat and learn more about Nature Medicine!

Our #genetics and #genetherapy editor Anna Maria Ranzoni is attending the virtual #ASGCT21 meeting this week. Get in touch if you'd like to chat and learn more about Nature Medicine!

It's #WorldCancerDay & we Nature Medicine are fortunate to work with the #CancerResearch community to share exciting & impactful #translational & #clinical studies on the prevention, diagnosis, treatment & survivorship of #cancer. Here’s a selection of papers published in 2022!🧵

Check out the joint Keystone Symposia conference on Precision Genome Engineering & Delivery of Nucleic Acid Therapeutics!🧬 Our editor Anna Maria Ranzoni will be there, reach out to her if you'd like to chat about your work. #KSGenomeEng24 hubs.la/Q026Mdwl0 hubs.la/Q026Md720

Our genetics editor Anna Ranzoni will be at the #KSGenomeEng25 conference in Killarney next week - get in touch with her if you'd like to talk about publishing your work! keysym.us/KSGenomeEng25