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Vikas Bansal
Scripps Health
$3,321,865
Attributed
$5,959,767
Total exposure
3
Grants
2
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 $952.3K · FY2013–25$1M$750K$500K$250K$0
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Funding mix
By agency
NIH$5,959,767 · 3
By mechanism
R01$5,483,442 · 2
R21$476,325 · 1
Top collaborators
- Vineet Bafna7 shared
- Melissa Gymrek7 shared
Others in their field
Top investigators on “Data Set”
- Lawrence Corey · Fred Hutchinson Cancer Center$424,653,591
- David R. Weir · University Of Michigan At Ann Arbor$412,781,191
- David Heimbrook · Leidos Biomedical Research, Inc.$409,886,450
- Margaret Juliana McElrath · Fred Hutchinson Cancer Center$348,905,121
- Gary D Acton · University Of California-Davis$320,373,312
- Mitchell J Malone · Texas A&M Research Foundation$320,373,312
Research focus
Data SetMalignant NeoplasmsHuman GeneticsDetectionTechnologyGenomeComplexGenome SequencingCodeGenotypeVariantHuman GenomeInsertion/Deletion MutationBiological SciencesGene DuplicationMutationHearing ImpairmentHereditary Nonpolyposis Colorectal NeoplasmsPms2 GeneGenetic VariationAlgorithmsDiploidyGenomicsWhole Genome
Grant awards (13)
Refining Mendelian disease analysis via detection of clinically relevant repeat variants$542,343
R01 · FY2025 · HG
Refining Mendelian disease analysis via detection of clinically relevant repeat variants$564,751
R01 · FY2024 · HG
Refining Mendelian disease analysis via detection of clinically relevant repeat variants$569,759
R01 · FY2023 · HG
Computational methods for variant calling and haplotyping using long-read sequencing technologies$380,962
R01 · FY2023 · HG · contact PI
Computational methods for variant calling and haplotyping using long-read sequencing technologies$381,631
R01 · FY2022 · HG · contact PI
Refining Mendelian disease analysis via detection of clinically relevant repeat variants$570,000
R01 · FY2021 · HG
Computational methods for variant calling and haplotyping using long-read sequencing technologies$382,268
R01 · FY2021 · HG · contact PI
Refining Mendelian disease analysis via detection of clinically relevant repeat variants$570,000
R01 · FY2020 · HG
Computational methods for variant calling and haplotyping using long-read sequencing technologies$381,728
R01 · FY2020 · HG · contact PI
Refining Mendelian disease analysis via detection of clinically relevant repeat variants$570,000
R01 · FY2019 · HG
Refining Mendelian disease analysis via detection of clinically relevant repeat variants$570,000
R01 · FY2018 · HG
Methods for detecting short indels from high-throughput sequence data$193,750
R21 · FY2014 · HG · contact PI
Methods for detecting short indels from high-throughput sequence data$282,575
R21 · FY2013 · HG · contact PI