Funding Opportunity PA-18-868 from the NIH Guide for Grants and Contracts. Genome-wide association studies have found many variants associated with disease risk, disease protection, or other traits. However, these studies generally identify many variants that are statistically associated with the trait, but do not show which variants in genomic elements cause these effects, or how they result in differences in function. Similarly, clinical genomic sequencing studies have identified many variants in healthy and diseased individuals, but the pathogenicity of such variants is usually unknown, leading to their classification as variants of uncertain significance (VUSs), which makes clinical implementation difficult. This program aims to support the development of generalizable approaches to study how genetic variants lead to differences in function, how such functional differences lead to disease processes, and how this knowledge can be used clinically.

Notice NOT-NR-18-013 from the NIH Guide for Grants and Contracts

Notice NOT-NR-18-014 from the NIH Guide for Grants and Contracts

Notice NOT-NR-18-015 from the NIH Guide for Grants and Contracts

Notice NOT-CA-18-095 from the NIH Guide for Grants and Contracts

Notice NOT-MH-18-037 from the NIH Guide for Grants and Contracts

Notice NOT-MH-18-038 from the NIH Guide for Grants and Contracts

Notice NOT-GM-18-039 from the NIH Guide for Grants and Contracts

Notice NOT-HL-18-639 from the NIH Guide for Grants and Contracts

Notice NOT-NS-18-075 from the NIH Guide for Grants and Contracts

Funding Opportunity RFA-RM-18-030 from the NIH Guide for Grants and Contracts. The purpose of this Funding Opportunity Announcement (FOA) is to establish one or two centers that can rapidly generate high quality whole genome sequence and variant data from a large number of human specimens representing two types of pediatric conditions - childhood cancers and structural birth defects. All sequence data generated under this FOA will be re-processed and harmonized by the Gabriella Miller Kids First Pediatric Data Resource Center (Kids First DRC), which is also charged with building a public-facing, web-based portal that will allow researchers to search, access, aggregate, analyze, and share annotated genomic sequence, variant, and phenotypic datasets. Together these resources will promote comprehensive and cross-cutting research and collaboration within the pediatric research community.

Negotiable: Paramount Recruitment: Senior Bioinformatician - Genomics England London Paramount are working in partnership with Genomics England to expand their team in order to deliver London, England

Notice NOT-AG-18-023 from the NIH Guide for Grants and Contracts

Negotiable: Paramount Recruitment: Lead Bioinformatician One of the country's leading Research Institutes has released an opportunity for a Senior Bioinformatician to develop a talented, multi-disciplinary informatics team. Oxfordshire, England

Notice NOT-OD-18-197 from the NIH Guide for Grants and Contracts

Notice NOT-TR-18-030 from the NIH Guide for Grants and Contracts

Notice NOT-NS-18-076 from the NIH Guide for Grants and Contracts

Notice NOT-HG-18-012 from the NIH Guide for Grants and Contracts

Notice NOT-NS-18-074 from the NIH Guide for Grants and Contracts

In Computer Science, Bioinformatics, Machine Learning, or a related field Preferred. Experience collaborating with interdisciplinary teams....
From Microsoft - Sun, 22 Jul 2018 14:00:29 GMT - View all Redmond, WA jobs