Character Biosciences的动态

?? Unlocking the Future of Genomic Analysis with the Stratys? System by Bionano! ?? Discover the cutting-edge capabilities of the Stratys? System, revolutionizing genomic analysis with unparalleled structural variant detection at scale. ?? Explore how the Stratys? System empowers researchers and clinicians to uncover complex genomic variations, driving breakthroughs in disease research, precision medicine, and beyond. Ready to elevate your genomic analysis? Learn more about the transformative potential of the Stratys? System today on : #Genetrics #Bionano #StratysSystem #GenomicAnalysis #PrecisionMedicine #HealthcareInnovation ??

Genome editing technologies has enabled modification of DNA sequences with unprecedented precision and efficiency.???Together with efficient platforms for ex vivo and in vivo delivery into cell types of interest, it offers an exciting possibility of tailored medicine to effect lasting curative therapies.????Recent advances in the technology landscape have paved the way for rapid development of new medicine for any genetic disease.?? This session brings together pioneers in the field who will share important perspectives on developing and delivering these novel approaches that navigate current manufacturing, clinical and regulatory challenges to achieve affordable therapies.? Bruce Levine Fyodor Urnov Laura Sepp-Lorenzino, Ph.D. Details on this and other concurrent session are available here:? https://lnkd.in/gnygA7n8

Curating clinically relevant interpretations of genetic variants can be challenging. Velsera's Clinical Genomics Workspace (CGW) is here to assist you! Our software equips your team with the latest medical data to ensure reliable interpretations and the best therapeutic options for the patient. CGW saves you time when analyzing genomic interpretations by: ??Structuring interpretations systematically for convenient review and modification. ??Remembering your decisions about past biomarker from previous cases to enable faster sign-out time. Interested in learning more? Watch the recording: https://lnkd.in/gBe6kBkD #NGS #PrecisionMedicine #EraOfVelsera #Genomics

Undoubtedly, advancements in genetics have transformed healthcare, making personalized medicine, early disease diagnosis, and targeted therapies a reality. However, the scientific journey to where we stand today has been anything but easy. In our latest post, Timeline of Human Genome Sequencing, we highlight the major figures and groundbreaking scientific initiatives that paved the way for these revolutionary developments in healthcare.

Quite the roster of leaders from Labcorp and Invitae going to these Becker's events! They'll discuss the role of lab data and genetic testing in personalized medicine. Learn more about the events here: https://lnkd.in/eswVktpg #GeneticTesting #PersonalizedMedicine #HealthcareInnovation

??Breakthrough in single-cell epigenetics Paired-Tag simultaneously profiles RNA and epigenetics - track cell states and communication in aging, disease, and beyond High-resolution insights with no cell sorting; find out more at https://epigenome.us #SingleCell #Epigenetics

Researchers have linked hundreds of genetic variants to coronary artery disease risk, but as with many conditions, probing the biological relationships between variants and risk remains challenging. Gavin Schnitzler, Helen Kang, Rajat Gupta, Jesse Engreitz and colleagues have developed and applied what they call a Variant-to-Gene-to-Program (V2G2P) approach which prioritizes the pathways shared by multiple risk loci. Using CRISPRi-Perturb-seq and machine learning, they found connections between CAD risk and 41 variants in endothelial cells, which line blood vessels. Several of these variants regulate endothelial cells' response to blood flow, and represent new CAD mechanisms. Learn more in Nature: https://lnkd.in/efcmYbNQ. #BroadInstitute #Science #ScienceNews #Research #ScientificResearch

Integration of population genetics (GWAS) and single-cell methods (Perturb-seq), and it's amazing! These approaches can bring computational/statistic results and highly complex biological contexts all together.

Centre for Genomic Regulation (CRG) It takes two to TANGO: New strategy to tackle fibrosis and scarring https://lnkd.in/dmF-Jpxn

??Breakthrough in single-cell epigenetics Paired-Tag simultaneously profiles RNA and epigenetics - track cell states and communication in aging, disease, and beyond High-resolution insights with no cell sorting; find out more at https://epigenome.us #SingleCell #Epigenetics