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Kai Wang

University Of Southern California

$10,901,792
Attributed
$14,537,327
Total exposure
8
Grants
5
Lead (contact PI)

Attributed= this PI's even-split share of every grant they're on (the fair, additive number). Exposure = full size of all those grants.

Funding over time

peak $2.7M · FY201225
$5M$3.8M$2.5M$1.3M$0
'12
'13
'14
'15
'16
'17
'18
'19
'20
'21
'22
'23
'24
'25

Funding mix

By agency

NIH$14,537,327 · 8

By mechanism

R01$12,912,886 · 6
OT2$1,156,956 · 1
R21$467,485 · 1

Top collaborators

Most similar at University Of Southern California

Same institution · by research overlap

Others in their field

Top investigators on “Genomics

Research focus

GenomicsBaseGenesGenomeVariantPhenotypeSoftware ToolsDesignDisease PhenotypeDetectionComputing MethodologiesCommunitiesInformaticsComputer SoftwareGeneticMalignant NeoplasmsBioinformaticsBenchmarkingGenetic VariantUniversitiesAlgorithmsInnovationInsertion/Deletion MutationResources

Grant awards (28)

Multimodal machine learning for diagnosis and mechanistic phenotyping of inherited diseases$1,156,956
OT2 · FY2025 · OD · contact PI
Fair Phenotype Annotation and Genomic Reinterpretation$880,069
R01 · FY2025 · HG
Novel bioinformatics methods to detect DNA and RNA modifications using Nanopore long-read sequencing$702,283
R01 · FY2025 · HG · contact PI
Fair Phenotype Annotation and Genomic Reinterpretation$880,069
R01 · FY2024 · HG
Novel bioinformatics methods to detect DNA and RNA modifications using Nanopore long-read sequencing$690,069
R01 · FY2024 · HG · contact PI
Fair Phenotype Annotation and Genomic Reinterpretation$886,418
R01 · FY2023 · HG
Novel bioinformatics methods to detect DNA and RNA modifications using Nanopore long-read sequencing$709,603
R01 · FY2023 · HG · contact PI
Detection and annotation of structural variants from long-read sequencing$440,000
R01 · FY2022 · GM · contact PI
Deep phenotyping in Electronic Health Records for Genomic Medicine$799,965
R01 · FY2021 · LM
Detection and annotation of structural variants from long-read sequencing$517,232
R01 · FY2021 · GM · contact PI
Deep phenotyping in Electronic Health Records for Genomic Medicine$799,965
R01 · FY2020 · LM
Detection and annotation of structural variants from long-read sequencing$440,000
R01 · FY2020 · GM · contact PI
Novel approaches to map DNA replication traffic in a genome-wide scale$205,308
R21 · FY2020 · HG
Detection and annotation of structural variants from long-read sequencing$77,232
R01 · FY2020 · GM · contact PI
Deep phenotyping in Electronic Health Records for Genomic Medicine$74,999
R01 · FY2020 · LM
Deep phenotyping in Electronic Health Records for Genomic Medicine$799,965
R01 · FY2019 · LM
Detection and annotation of structural variants from long-read sequencing$440,000
R01 · FY2019 · GM · contact PI
Novel approaches to map DNA replication traffic in a genome-wide scale$262,177
R21 · FY2019 · HG
Deep phenotyping in Electronic Health Records for Genomic Medicine$799,949
R01 · FY2018 · LM
UNDERSTANDING THE FUNCTIONAL IMPACTS OF GENETIC VARIANTS IN MENTAL DISORDERS$430,000
R01 · FY2018 · MH · contact PI
UNDERSTANDING THE FUNCTIONAL IMPACTS OF GENETIC VARIANTS IN MENTAL DISORDERS$381,539
R01 · FY2017 · MH · contact PI
Understanding the functional impacts of genetic variants in mental disorders$396,250
R01 · FY2016 · MH · contact PI
Integrated Variation Detection Annotation and Analysis$227,298
R01 · FY2016 · HG · contact PI
Integrated variation detection annotation and analysis for high-throughout seque$127,481
R01 · FY2016 · HG · contact PI
Integrated variation detection annotation and analysis for high-throughout seque$353,567
R01 · FY2015 · HG · contact PI
Integrated variation detection annotation and analysis for high-throughout seque$354,302
R01 · FY2014 · HG · contact PI
Integrated variation detection annotation and analysis for high-throughout seque$344,564
R01 · FY2013 · HG · contact PI
Integrated variation detection annotation and analysis for high-throughout seque$360,067
R01 · FY2012 · HG · contact PI