The NIH-funded ROSALIND Diagnostic Monitoring platform has just been launched to provide test developers and regulators with rapid and regular updates about SARS-CoV-2 variants of concern and their distribution and assess the impact of these variants on available diagnostic test performance.
Company has now raised $210M in three years with plans to build the world's largest library of clinical and molecular data for clinical use
Adoption of clinical genomics applications has been driven by increasingly scalable genomic technologies. Higher-throughput approaches to genetic testing have resulted in increased diagnostic yields and discovery coupled with advances in bioinformatic analysis tools.
New partnership comes two months after CancerLinQ and ONS launch CancerLinQ Ambassadors Program, a national practice engagement initiative.
Geisinger researchers will tap data of more than 90,000 whole-exome sequences from MyCode of patients with ARVC-related genetic findings
Collaboration aimed at improving the accuracy of data analysis for chromatin immunoprecipitation (ChIP) sequencing experiments.
Syntropy’s platform will be designed to facilitate secure, transparent sharing of data between participating researchers and institutions.
Researchers at the University of Edinburgh and the European Bioinformatics Institute at the European Molecular Biology Laboratory (EMBL-EBI) have introduced a new diagnostic genome-wide...
Known as Summix, the method adjusts information to match the ancestry of a person or sample of people with the goal of making large genetic databases more useful for people of traditionally underrepresented ancestries.
David FitzPatrick’s typical patient is a toddler with global developmental delay who is small for her age, has epilepsy, and cannot speak or understand...