Just over a week left!
Submit your abstract for the Cardiac Precision Medicine in the 21st Century Conference ���
📅 Oct 29–31, 2025 | Toronto
Showcase your research + compete for Best Abstract Award!
🔗 https://t.co/qCbmHy9dnp
#CardiacPrecision #Genomics #callforabstracts
🔬New in #CHD research! Nearly 90% of cases remain genetically undiagnosed, but @RobLesurf and an international team led by @seema_mital at @SickKids have developed a new #AI model to detect genetic variants. Read about this leap in #precisionmedicine!
🔗 https://t.co/05QXExqQMY
Great day at the @trogersresearch Heart Failure Symposium learning about the latest discoveries, insights, and innovations in cardiovascular science!Exciting to see many of our collaborative research work from the @seema_mital lab presented. Check out some of our fav moments
A validated heart-specific model for splice-disrupting variants in childhood heart disease! 🫀🧬
@seema_mital@RobLesurf and team's machine learning model outperformed SpliceAI for predicting cardiac-specific splice-disrupting variants.
@medrxivpreprint
https://t.co/jZENECta4f
Great and educational day at the @trogersresearch Heart Failure Symposium!
Team member @RobLesurf, Senior Bioinformatician of @seema_mital lab presented a machine learning model identifying cryptic splice-disrupting variants that contribute to the genetic etiology of CHD 🧬🫀
Please join us for the Sick Kids and @PacBio Revio Launch Event on July 26th! We have a stellar line-up of lightning talks, food and refreshments as well as time to network. #PacBio#jointhereviolution#revio.
Spotted in Romania for the @ERANET_PerMed symposium! @Seemamital provided updates and results of the PROCEED (Personalized genomics for congenital heart disease) consortium. @RobLesurf presented new findings in genetics of CHD!
Attending ASHG 2022? Come say hi and learn about cryptic splice variants in congenital heart disease this Wed Oct 26th 3-4:45pm, Poster Hall South Building Level 1, poster PB2951 @hcbiobank
I'm going to visit my 98-year old grandmother in hospital and was told by @MackenzieHealth today that rapid tests there are "only for employees". This is backwards and wrong. @celliottability@YorkRegionGovt@fordnation please fix this.
Very proud to share our study preprint 'Whole genome sequencing delineates regulatory and novel genic variants in childhood cardiomyopathy'! https://t.co/qObZ3x3jEW
We are looking to hire someone to join the @CIViCdb team as an expert editor/curator (PhD/Senior Scientist level). Please contact @obigriffith and myself if you are interested in joining a dynamic, international team of clinicians and basic researchers.
Let’s play a little game.
Let’s say that you’re the CSO at a cancer pharma company, and you have to choose a target to go after.
Here’s a gene – high expression is associated with poor prognosis in brain cancer. Looks like a good candidate for an inhibitor right?