@myESMO Recommendations for clinical reporting of genomics - now published in @Annals_Oncology. We're aiming to advance rational, evidence-based use of genomics in patient care and harmonize biomarker interpretation in cancer treatment
https://t.co/GohY3dWkQB
Here’s the newest and final version:
𝘀𝗻𝗣𝗔𝗧𝗛𝗢-𝘀𝗲𝗾: unlocking the pathology archives
A method/protocol that works very well, has been widely accepted and embraced by scientists globally, yet not as much by peer-reviewed journals. https://t.co/VISRUEtrtO
@AedinCulhane Agree 100%, would be interested to see data to support 500 vs. 50 gene panels in terms of cost + scaling. Also entirely agree that making clinically generated data accessible to research community is necessary.
Today, we launch the National Strategy for Accelerating Genetic and Genomic Medicine in Ireland which outlines the approach for developing a patient and family centred #genetic and #genomic service.
https://t.co/IarvE2S6mH
@nilshomer You can't know everything. Draw mental boundaries based on your interests. Use new projects to redraw boundaries by learning something you think will be useful if time permits (IMO it always should).
Out now in @genomeresearch - our comprehensive analysis of the effects of aneuploidy on protein expression. Changes in gene dosage trigger complex compensatory mechanisms that are conserved from yeast to cancer! Great work led by @DrKlaske.
https://t.co/D3G6GlNIhA
recount3, from @chrisnwilks. @KasperDHansen, @BenLangmead & co, is a resource of 750,000 mouse and human RNA-seq datasets uniformly processed with the same pipeline. It allows rapid queries across the whole dataset, eg cross-species or cross-study https://t.co/exV5YP1ugr
🆕@CD_AACR
Functional STK11 mutations is associated with resistance to ICIs in #lungcancer & is reversed by STAT3 knockdown 🌟 #LCSM
https://t.co/vKnWE5toDW
Announcing the @ClinGenResource Criteria Specification Registry https://t.co/5ot7AITS3X, a database for the management of the Criteria Specifications of @TheACMG evidence codes for variant classification from ClinGen Variant Curation Expert Panels #variantclassification
🎉200+ authors came together to deliver the latest issue of @cellgenomics, featuring GA4GH-enabled interop. These papers represent years of tireless effort from a truly global community; we are deeply grateful to each of you. https://t.co/QQwLNV1Vmh
Our work developing Repair-seq, a platform for studying #DNArepair processes, and its application to double-strand breaks is out today @CellCellPress. Alongside, we release https://t.co/7aIPds1XEl, a portal for exploring many, many DNA repair phenotypes! https://t.co/6IizvfCdt3
1/ What are the challenges ahead for multi-modal data integration to improve precision oncology? In this @NatureRevCancer perspective we outline how we might leverage diagnostic cancer data as a substrate for next generation integrative biomarkers. https://t.co/Qpfjwb7GYr
Next-generation immunotherapy: what's next after anti-PD-1/PD-L1 and anti-CTLA4, how to increase the chance of success of novel immuno-oncology strategies in the clinic, and moving towards personalized immuno-medicine. A great review by @merghout and team! https://t.co/LPcJ4jfUsI
Clinical challenges in Genomic Medicine for Cancer Care | 15 Oct
Register now for this free webinar⬇️
https://t.co/OtzUkS1qXU
#GCchat#genetictesting#genetics#genomics