We are collaborating with Foundation Medicine to deliver genomic profiling to patients in our lunresertib clinical trials and beyond. We are thrilled to take this next step with the global leader in companion diagnostic approvals for next generation sequencing testing, with the potential to develop a companion diagnostic and expand access to clinical trial sites for our global lunresertib program. Learn more here: https://lnkd.in/enRH_8eA #precisiononcology #clinicaltrials #companiondiagnostic #PKMYT1inhibition
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attending Esmo, visit this poster to see real implementation of the most comprehensive genomic panel #CGP with better results than TSO500, easy process, and a failure rate less than 5% in routine
Head & Assistant Professor - Molecular Diagnostics & Research (Div. of Translational Pathology, GDI - Cancer Research Lab)
Day #3 of #ESMO23 in Madrid 🇪🇦: Please stop by poster 1253P if you are interested in #PrecisionOncology. Happy to discuss the capabilities of comprehensive genomic profiling and our implementation of OncoDNA OncoDEEP for precision diagnostics (HRD, TMB, MSI etc.) in clinical routine.
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Global Scientific Director Integrated Healthcare Solutions, Personalized Medicine Oncology chez Roche
Great research and evidence to continuously improve patient care.
With over 20 pieces of research, we’re excited to share new data around the emerging applications of our liquid biopsy & monitoring portfolio, as well as studies investigating new biomarkers and the expanding utility of comprehensive genomic profiling, including Foundation Medicine’s new RNA test. Click the link to learn more about everything we’re presenting at #ASCO24: https://bit.ly/3WNlYdJ
Foundation Medicine at 2024 ASCO® Annual Meeting
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Innovative Leader | Connector | Motivator | People Focused | Problem Solver Extraordinaire | Product Launch Wizard | 21 years of striving for excellence
Our data at ASCO this year highlights the important role genomic profiling plays in cancer care and research and can be grouped into four major buckets: - Emerging Applications of Liquid Biopsy Using FoundationOne®Liquid CDx and FoundationOne®Tracker. - Utility of CGP in Earlier Stages of Disease, Rare Cancers, and Using RNA Sequencing. - New CGP Biomarkers, Including Homologous Recombination Deficiency (HRD) Signature and Methyl Thioadenosine Phosphorylase (MTAP) Genomic Loss. - Impact of Ancestry on the Genomic Alteration Landscape.
With over 20 pieces of research, we’re excited to share new data around the emerging applications of our liquid biopsy & monitoring portfolio, as well as studies investigating new biomarkers and the expanding utility of comprehensive genomic profiling, including Foundation Medicine’s new RNA test. Click the link to learn more about everything we’re presenting at #ASCO24: https://bit.ly/3WNlYdJ
Foundation Medicine at 2024 ASCO® Annual Meeting
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🌟 Exciting news for smaller labs looking to adopt NGS! 🌟 A new cloud-based secondary analysis solution for oncology and inherited disease applications enables labs to process more sequencing data without extensive time and resource investment. Agnostic for use with any panel, scalable to any case volume, and ISO 27001-, GDPR- and HIPAA-compliant, this new secondary analysis solution is breaking speed and cost barriers in #NGS testing. Learn more ⬇️ #Genomics #SmallLabs #Accessibility #GeneticTesting #NGSAnalysis #ClinicalNGS
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Ahead of the curve…
With over 20 pieces of research, we’re excited to share new data around the emerging applications of our liquid biopsy & monitoring portfolio, as well as studies investigating new biomarkers and the expanding utility of comprehensive genomic profiling, including Foundation Medicine’s new RNA test. Click the link to learn more about everything we’re presenting at #ASCO24: https://bit.ly/3WNlYdJ
Foundation Medicine at 2024 ASCO® Annual Meeting
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Did you know? Next-Generation Sequencing (NGS) in clinical settings has revolutionized personalized medicine by enabling comprehensive genomic analysis in a fraction of the time compared to traditional methods. Efficient analysis and interpretation of NGS data is very much important to get informed decision on disease diagnostics and treatment. Join our upcoming workshop to get answers to all your questions related to NGS and it's applications in Clinic! Hurry up... early bird discount ends on March 12th!! For registration and more details, visit https://lnkd.in/dkVH735N #precisionmedicine #nextgenerationsequencing #bioinformatics
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🎉It’s RNA Day!🎉 Let's celebrate U with 50% off select streamlined KAPA RNA HyperPrep Kits! The workflow, including ribodepletion, can now be completed in about 5 hours—making more time for U! Learn more: http://spkl.io/60424i4C4 #DrugDiscovery #RNAseq #PrecisionMedicine #CancerResearch #TranslationalResearch #NGS #LibraryPrep #NextGenSequencing #Sequencing #Genomics For Research Use Only. Not for use in diagnostic procedures.
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It is critical that DNA-based genomic profiling (CGP) tests are optimally designed to identify fusions, which are important driver events that can significantly influence treatment decisions & patient outcomes. #NewResearch demonstrates that robust detection of fusions is possible using carefully designed DNA-based sequencing methodologies and, in an analysis of nonsquamous NSCLC, that fusions detected using high-quality DNA CGP assays are associated with clinical benefit from matched targeted agents. Read more in our latest research spotlight: https://bit.ly/49N1x3R
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Sr. Sales Specialist, Single Cell Multiomics - Northeast || ACE CPT/ASFA Master Health & Wellness Coach || Opinions are my own
Hot off the presses, our newest case study highlights how RNA-seq can be employed in retrospective clinical trials. Click the link below to read how RNAseq helped uncover a potential biomarker of Selinexor response in DD-LPS patients. If you want to learn more about how the sequencing capabilities at Discovery Life Sciences can aid your clinical studies and research, don't hesitate to reach out. #clinicalresearch #immunooncology #rnaseq #drugdevelopment #clinicaltrials
Retrospective RNA Sequencing of Dedifferentiated Liposarcoma Phase II-III Clinical Trial Patients Reveals a Potential Biomarker of Selinexor Response
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Implementing comprehensive rapid genomic testing into your diagnostic evaluation can return results—and help you better address your patients’ unique needs—in as little as 5 days. For acutely and critically ill babies, using rapid whole genome sequencing (rWGS) as a first-tier test can influence clinical management, reduce overall healthcare costs, and prevent a diagnostic odyssey. #NICUAwareness #NICUAwarenessMonth #NICUWarriors #NICU #GenomicSequencing #GenomeSequencing #GeneticTesting
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Healthcare Commercialization Partner for Biotech, Biopharma, Med Device & Med Tech
1moThis sounds like a great collaboration!