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NIH funding notice PAR-21-254

Investigator Initiated Research in Computational Genomics and Data Science (R01 Clinical Trial Not Allowed)

Closed on January 7, 2025.

Posted
July 29, 2021
Close date
January 7, 2025
Activity codes
Not stated on the notice page
Institutes taking part
Not stated on the notice page

Read the notice on Grants.gov · NIH Guide page

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: $21,654,970 in first-year total cost, median $619,540.

Most frequent study sections

  1. Biodata Management and Analysis Study Section[BDMA]7
  2. Genomics, Computational Biology and Technology Study Section[GCAT]5
  3. Genetic Variation and Evolution Study Section[GVE]3
  4. Special Emphasis Panel[ZRG1 BBBT-M (84)]2
  5. Analytics and Statistics for Population Research Panel A Study Section[ASPA]1

Most frequent institutions

  1. JOHNS HOPKINS UNIVERSITY2
  2. UNIVERSITY OF CALIFORNIA BERKELEY2
  3. BOSTON MEDICAL CENTER1
  4. COLD SPRING HARBOR LABORATORY1
  5. DANA-FARBER CANCER INST1
Competing awards under PAR-21-254 and the notices it replaced
FYProjectPIsInstitutionFirst-year costStudy section
2025Scalable software engineering and methods for large-scale subcellular spatial omics1R01HG014487-01DRIES, RUBENBOSTON MEDICAL CENTER, MA$3,371,645ZRG1
2025Computational and Statistical Methods for Genetic Association Studies of Disease Course Over Time1R01HG014518-01ZHOU, WEIMASSACHUSETTS GENERAL HOSPITAL, MA$3,287,168GCAT
2025Experimental-data-based in-silico data generation platform to improve the accuracy and reliability of single-cell and spatial omics data analysis1R01HG014687-01LI, JINGYI JESSICAFRED HUTCHINSON CANCER CENTER, WA$2,409,233ZRG1
2025Personal and panel references for improved alignment2R01HG011392-06LANGMEAD, BENJAMIN THOMASJOHNS HOPKINS UNIVERSITY, MD$2,349,722ZRG1
2025Non-B DNA structure discovery and function assessment using nanopore translocation times1R01HG014255-01AGUIAR, DEREK C.UNIVERSITY OF CONNECTICUT STORRS, CT$805,000MSFB
2025Deep learning for population genetics2R01HG010774-05A1KERN, ANDREW DUNIVERSITY OF OREGON, OR$715,759GVE
2025Extending the utility and performance of variant effect predictors with protein language models1R01HG013524-01A1NTRANOS, VASILEIOSUNIVERSITY OF CALIFORNIA, SAN FRANCISCO, CA$687,063GVE
2025Predicting individual disease risk for individuals harboring monogenic risk alleles with deep learning1R01HG013511-01A1JORDAN, DANIEL MICHAELICAHN SCHOOL OF MEDICINE AT MOUNT SINAI, NY$579,403ASPA
2025Calling germline and mosaic variants from long genomic and RNA-seq reads1R01HG014175-01LI, HENGDANA-FARBER CANCER INST, MA$501,618BDMA
2024Fast, powerful, scalable, usable, and distributable methods for multi-modal single cell analyses1R01HG013317-01GREENLEAF, WILLIAM JAMESSTANFORD UNIVERSITY, CA$702,003BDMA
2024Enabling comprehensive and user-friendly circular RNA analyses with circtools.cloud1R01HG013124-01A1JAKOBI, TOBIASUNIVERSITY OF ARIZONA, AZ$660,671BDMA
2024Fully Realizing Pangenomics Alignment1R56HG013865-01BOUCHER, CHRISTINALANGMEAD, BENJAMIN THOMASUNIVERSITY OF FLORIDA, FL$644,578ZRG1
2024A unified probabilistic model and software implementation for analysis of nascent RNA sequencing data1R01HG012944-01A1SIEPEL, ADAM CHARLESCOLD SPRING HARBOR LABORATORY, NY$594,501GCAT
2024Scalable Computational Methods for Genealogical Inference: from species level to single cells1R01HG013117-01A1HOLMES, IAN HNIELSEN, RASMUSSONG, YUN SUNIVERSITY OF CALIFORNIA BERKELEY, CA$592,707GVE
2024Deep integrative analysis of Hi-C data1R01HG013321-01A1WANG, SHENGUNIVERSITY OF WASHINGTON, WA$504,949BDMA
2024Analytical Infrastructure for Multiple Sample Single Cell Genomic Data1R01HG013409-01A1JI, HONGKAIJOHNS HOPKINS UNIVERSITY, MD$361,069BDMA
2023Specialized Tools and Auto-updatable Scalable Interactive Databases to Study isomiRs, tRFs and rRFs in Human and Mouse1R01HG012784-01A1RIGOUTSOS, ISIDORETHOMAS JEFFERSON UNIVERSITY, PA$553,060BDMA
2023Title: Functional Annotation of Genomes via Phenotypic Convergence within Large Multi-species Alignments2R01HG009299-06A1CHIKINA, MARIA DCLARK, NATHANIEL LUNIVERSITY OF PITTSBURGH AT PITTSBURGH, PA$529,944GCAT
2023Mendelian randomization for modern data: Integrating data resources to improve accuracy of causal estimates.1R01HG013104-01MORRISON, JEAN V.UNIVERSITY OF MICHIGAN AT ANN ARBOR, MI$358,755GCAT
2023Scalable Computational Methods for Genealogical Inference: from species level to single cells1R56HG013117-01HOLMES, IAN HNIELSEN, RASMUSSONG, YUN SUNIVERSITY OF CALIFORNIA BERKELEY, CA$315,000ZRG1
2022Development and Application of Computational Methods for Single Cell DNA Sequencing Data1R01HG012573-01PARK, PETER JHARVARD MEDICAL SCHOOL, MA$747,149GCAT
2022Novel methods for large-scale genomic interval comparison1R01HG012558-01SHEFFIELD, NATHANUNIVERSITY OF VIRGINIA, VA$383,973BDMA

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.

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PAR-21-254: Investigator Initiated Research in Computational Genomics and Data Science (R01 Clinical Trial Not Allowed) | ScienceDex | ConductScience