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Event
NHGRI is hosting a workshop - Identifying Research Priorities to Accelerate genetic Diagnosis - on April 16-17, 2024.
… - Break 4:10 PM – Session 5: Computational Tools to Enable Genetic Diagnoses Moderator: Chris Wellington, NHGRI 4:10 PM … much work remains to advance our understanding of the genetic cause of Mendelian conditions and to increase the … Drive … Identifying Research Priorities to Accelerate Genetic Diagnosis … NHGRI is hosting a workshop - Identifying …
Research Funding
The GREGoR (formerly the Mendelian Genomics Research Consortium) is aimed at significantly increasing the proportion of Mendelian disorders with an identified genetic cause through enhanced data sharing, collaboration and an increased focus on the application of new technologies, sequencing strategies and analytical approaches.
… website . … Identifying Research Priorities to Accelerate Genetic Diagnosis April 16-17, 2024 GREGOR Pre-Application … the proportion of Mendelian disorders with an identified genetic cause through enhanced data sharing, collaboration … the proportion of Mendelian disorders with an identified genetic cause through enhanced data sharing, collaboration …
Event
On Tuesday, February 6, 2024, the National Human Genome Research Institute hosted an eConsult webinar to provide an overview of three notice of funding opportunities (RFA-HG-24-001, PAR-24-106 and PAR-24-107). Questions were answered during the webinar.
… is not selected for funding.   Can consultants order genetic tests for the patient? No. In an eConsult, the … own patient. If the consultant is needed to order the genetic test, this would be a referral.   Can some eConsults … to, address.   Can the service use non-physicians, such as genetic counselors, PharmDs, nurses, or PhDs to respond to …
FAQ
On October 10, 2024, NHGRI hosted a pre-application webinar for the Population Genomic Screening in Primary Care NOFOs: RFA-HG-24-021, RFA-HG-24-022, and RFA-HG-24-023. These FAQs contain questions answered during that webinar.
… expected to do data cleaning that links clinical data with genetic data? Yes, in collaboration with the CGs and SeqC. … assigned to the CGs for the clinical data and SeqC for the genetic data. The CC will be responsible for linking the clinical data with the genetic data.   Will statistical resources be available …
FAQ
Questions and answers to help applicants responding to the ML/AI Tools to Advance Genomic Translational Research (MAGen) notice of funding opportunities (NOFOs): RFA-HG-24-004 and RFA-HG-24-005.
… enhance the prediction of how individuals with pathogenic genetic variants manifest disease—the goal of this NOFO—but …