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Project

Component

27 items
networks
HG012047
IGVF
current
Defining causal roles of genomic variants on gene regulatory networks with spatiotemporally-resolved single-cell multiomics
ff554121-5ddd-4c0a-93fb-0809f389d170
predictive modeling
HG012022
IGVF
current
Supporting IGVF by modeling genetics, function, and phenotype with machine learning
f81dd63f-dc65-4e46-96b8-2d44f9456181
predictive modeling
HG012009
IGVF
current
Predicting the impact of genetic variants, genes and pathways on human disease
e367d3d4-bf15-4821-99d6-055e52910bc9
networks
HG012103
IGVF
current
Deciphering the Genomics of Gene Network Regulation of T Cell and Fibroblast States in Autoimmune Inflammation
df3cd6b4-dba8-40c7-8f44-3c8f94e2fe24
functional characterization
HG012053
IGVF
current
High-Throughput Functional Annotation of Gene Regulatory Elements and Variants Critical to Complex Cellular Phenotypes
cfdf836c-b9b5-4714-aa92-058214998cfc
data coordination
HG012012
IGVF
current
A Data and Administrative Coordinating Center for the Impact of Genomic Variation on Function Consortium
c933e5d0-f381-462b-bf42-e640e77f46fd
mapping
HG012076
IGVF
current
Single-cell Mapping Center for Human Regulatory Elements and Gene Activity
c62af563-4954-4172-984b-11883485119b
functional characterization
HG011972
IGVF
current
Stanford Center for Connecting DNA Variants to Function and Phenotype
c0c27048-195d-4754-98c5-b513a1a4d2c0
mapping
HG011986
IGVF
current
A foundational resource of functional elements, TF footprints and gene regulatory interactions
b4493512-d006-4cd2-b004-385979a91eac
functional characterization
HG011996
IGVF
current
Multiscale functional characterization of genomic variation in human developmental disorders
a7485ebf-8238-4d36-8e1d-203fefd85595
predictive modeling
HG012069
IGVF
current
Predicting context-specific molecular and phenotypic effects of genetic variation through the lens of the cis-regulatory code
9ff6df18-d3fd-4aa0-89e9-53a1449ee240
functional characterization
HG011966
IGVF
current
Massively parallel characterization of variants and elements impacting transcriptional regulation in dynamic cellular systems
85522f5c-3617-4a2c-9f01-c8740b60f401
Community
community
current
Community
704e156b-addc-4f16-81f0-8ffd36eef723
data coordination
HG012070
IGVF
current
WashU-Northwestern Genomic Variation and Function Data and Administrative Coordinating Center
5f62347b-fa5c-4b05-b146-b5da565b9f83
predictive modeling
HG012064
IGVF
current
Predictive Modeling of the Functional and Phenotypic Impacts of Genetic Variants
52fd80a2-07fa-4aba-b06b-dc13e6bee3e5
functional characterization
HG012010
IGVF
current
Comprehensive characterization of variants underlying heart and blood diseases with CRISPR base editing
44651e8f-e2f2-4b51-b1a4-334d4d1c93c0
networks
HG012041
IGVF
current
Linking genome variation to transcriptional network dynamics in human B cells
41335c62-9e4b-4ae1-8fe9-17f4b5324f78
networks
HG012079
IGVF
current
Leveraging genetic variation to dissect gene regulatory networks of reprogramming to pluripotency
2f2c3b3d-5cea-4525-adb3-025bebb127df
mapping
HG012077
IGVF
current
Center for Mouse Genomic Variation at Single Cell Resolution
289740c5-e032-490d-9aac-88a7fdb6a589
networks
HG012059
IGVF
current
The impact of genomic variation on environment-induced changes in pancreatic beta-cell states
2234214f-36a7-4b95-b9b4-9c799933e5ac
functional characterization
HG012003
IGVF
current
Systematic in vivo characterization of disease-associated regulatory variants
1c2078f3-8e35-4ed5-9f12-3356ec3b7420
functional characterization
HG011989
IGVF
current
Molecular phenotyping of ~100,000 coding variants across Mendelian disease genes
1a6090bb-a7dc-497a-b0d0-f6c9b9c634ab
networks
HG012051
IGVF
current
Genomic control of gene regulatory networks governing early human lineage decisions
17d8d414-8a80-4fc0-879e-219eedc9cd7d
functional characterization
HG011969
IGVF
current
The Center for Actionable Variant Analysis; measuring variant function at scale
14e237c9-f0e1-4296-ab13-472de0588e2e
predictive modeling
HG011967
IGVF
current
Design, prediction, and prioritization of systematic perturbations of the human genome
1098f89c-a008-47a8-a8da-39e983ab6d37