Excited to unveil the groundbreaking work Wobble Genomics Ltd is doing now that we've emerged from stealth mode: we are now able to see cancer in a way that has never been seen before.
Today at the Early Detection of Cancer Conference (EDCC) in San Francisco, we're presenting our innovative diagnostics platform using long read RNA sequencing. From our prospective breast cancer clinical study, we've demonstrated ability to detect rare full-length RNA transcript variants not picked up by other methods. By leveraging these full-length transcripts as biomarkers, we achieved 80% sensitivity and 95% specificity in early-stage breast cancer detection.
This breakthrough enables us to distinguish cancer-associated RNA sequences from controls and discover new, unique transcripts, paving the way for a strong predictive diagnostic for early-stage breast cancer—arguably one of the most challenging cancers to diagnose via liquid biopsy.
Read our full press release for more detail: https://lnkd.in/deKsv3WH
If you're attending EDCC and want to learn more about our results, join our Founder and CEO, Dr. Richard Kuo and Chief Medical Officer, Dr. Richard Hockett at the poster session today at from 15:10-15:55.
A huge thank you to the entire Wobble Genomics Ltd for their work in achieving these milestones. And special thanks to the team at M+F Health (Anna Hollaway, Claudia Bolouri, Kirsty Clark, Jonathan Baily & Georgia Bron) for their exceptional support during our emergence from stealth mode.
There are more exciting developments ahead! 👀
#EdxConf24