The notices it replaced
Its page was not saved, so the notices it replaced are not known.
Who won it before
22 competing awards (new and renewals) from FY2014 to FY2025 under this notice and the notices it replaced: $10,750,622 in first-year total cost, median $482,486.
Most frequent study sections
- Biodata Management and Analysis Study Section[BDMA]8
- Genomics, Computational Biology and Technology Study Section[GCAT]5
- Genetic Variation and Evolution Study Section[GVE]4
- Biostatistical Methods and Research Design Study Section[BMRD]2
- Biomedical Computing and Health Informatics Study Section[BCHI]1
Most frequent institutions
- JOHNS HOPKINS UNIVERSITY2
- UNIVERSITY OF OREGON2
- BROAD INSTITUTE, INC.1
- CARNEGIE-MELLON UNIVERSITY1
- CHILDREN'S RESEARCH INSTITUTE1
| FY | Project | PIs | Institution | First-year cost | Study section |
|---|---|---|---|---|---|
| 2022 | Grammar-Driven Genomic Data Visualization1R01HG011773-01A1 | GEHLENBORG, NILS | HARVARD MEDICAL SCHOOL, MA | $607,236 | BDMA |
| 2022 | Cross-platform structural variant discovery with deep learning1R01HG012467-01 | POPIC, VICTORIA | BROAD INSTITUTE, INC., MA | $593,860 | BMRD |
| 2022 | Mining Thousands of Genomes to Classify Somatic and Pathogenic Structural Variants1R01HG011774-01A1 | LAYER, RYAN M | UNIVERSITY OF COLORADO, CO | $578,543 | BDMA |
| 2022 | Improved genomic sketching for MUMmer and metagenomics1R01HG012470-01 | KINGSFORD, CARLETON LEEMARÇAIS, GUILLAUME | CARNEGIE-MELLON UNIVERSITY, PA | $484,364 | GCAT |
| 2022 | Interpretable Computational Models of Functional Genomics Data1R01HG012131-01A1 | KOO, PETER K | COLD SPRING HARBOR LABORATORY, NY | $417,299 | GCAT |
| 2021 | Characterizing the evolutionary architecture of complex disease within and across diverse populations1R01HG012133-01 | MANCUSO, NICHOLAS | UNIVERSITY OF SOUTHERN CALIFORNIA, CA | $725,512 | GVE |
| 2021 | Scaling up computational genomics with tree sequences1R56HG011395-01A1 | RALPH, PETER LOCHHEAD | UNIVERSITY OF OREGON, OR | $556,834 | GVE |
| 2021 | Integrating genomic and clinical data to predict disease phenotypes using heterogeneous ensembles1R01HG011407-01A1 | PANDEY, GAURAV | ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI, NY | $539,951 | BCHI |
| 2021 | Novel Use of Genome Information to Understand Mutations1R01HG012117-01 | JERNIGAN, ROBERT LKLOCZKOWSKI, ANDRZEJ | IOWA STATE UNIVERSITY, IA | $480,608 | ZRG1 |
| 2021 | The pursuit of genetic causal mechanisms1R56HG010812-01A1 | SABATTI, CHIARA | STANFORD UNIVERSITY, CA | $455,280 | BMRD |
| 2021 | Using Syntenic Gapped-kmer Composition to Detect Conserved Enhancers where Sequence Alignment Fails1R56HG012110-01 | BEER, MICHAEL A | JOHNS HOPKINS UNIVERSITY, MD | $388,975 | GCAT |
| 2020 | Scalable detection and interpretation of structural variation in human genomes1R01HG010757-01A1 | QUINLAN, AARON R | UNIVERSITY OF UTAH, UT | $692,048 | BDMA |
| 2020 | Next Generation Computational Tools for Functional Genomics1R01HG011139-01 | IRIZARRY, RAFAEL ANGEL | DANA-FARBER CANCER INST, MA | $665,458 | GCAT |
| 2020 | Deep learning for population genetics1R01HG010774-01A1 | KERN, ANDREW D | UNIVERSITY OF OREGON, OR | $529,154 | GVE |
| 2020 | Enhancing open data sharing for functional genomics experiments: Measures to quantify genomic information leakage and file formats for privacy preservation1R01HG010749-01A1 | GERSTEIN, MARK BENDER | YALE UNIVERSITY, CT | $523,409 | BDMA |
| 2020 | Refining mutation rates and measures of purifying selection with an application to understanding the impact of non-coding variation on neuropsychiatric diseases1R01HG010773-01A1 | HE, XINNOVEMBRE, JOHN | UNIVERSITY OF CHICAGO, IL | $416,226 | GVE |
| 2020 | Computational methods for variant calling and haplotyping using long-read sequencing technologies1R01HG010759-01A1 | BANSAL, VIKAS | UNIVERSITY OF CALIFORNIA, SAN DIEGO, CA | $381,728 | BDMA |
| 2020 | Personal and panel references for improved alignment1R01HG011392-01 | LANGMEAD, BENJAMIN THOMAS | JOHNS HOPKINS UNIVERSITY, MD | $381,528 | BDMA |
| 2020 | Advancing Multi-Omics and Electronic Health Records Computational Methodologies1R01HG011138-01 | GAMAZON, ERIC R | VANDERBILT UNIVERSITY MEDICAL CENTER, TN | $330,670 | BDMA |
| 2020 | An interactive tool for in-depth and reproducible analysis of RNA-seq data1R01HG010805-01A1 | GE, XIJIN | SOUTH DAKOTA STATE UNIVERSITY, SD | $179,821 | BDMA |
| 2019 | Modeling Functional Elements using CRISPR Screening1R01HG010753-01 | LI, WEI | CHILDREN'S RESEARCH INSTITUTE, DC | $446,250 | GCAT |
| 2019 | Secure and Privacy-preserving Genome-wide and Phenome-wide Association Studies via Intel Software Guard Extensions (SGX)1R01HG010798-01 | TANG, HAIXUWANG, XIAOFENG | TRUSTEES OF INDIANA UNIVERSITY, IN | $375,868 | ZRG1 |
Data: Grants.gov's daily extract and NIH's notice pages and award files, in ScienceGraph release conductgrants-2026-11-09-0.1.0. An award is listed only where NIH's own record names the notice, and a PI only by NIH's profile ID. Grants.gov and NIH do not endorse ScienceDex.