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Paper Details

Atlas of primary cell-type-specific sequence models of gene expression and variant effects.
Cell Rep Methods
2
2023
ClinVar clinical variants, Human, cell types, common, genes, genome, human, noncoding space, primary cell types, primary cell-type-specific sequence models, primary human cell types, primary human cells, specialized cell types
Author NameAffiliation
Chandra L TheesfeldLewis-Sigler Institute for Integrative Genomics, Princeton University
Aaron K WongFlatiron Institute, Simons Foundation
Kara DolinskiLewis-Sigler Institute for Integrative Genomics, Princeton University
Kara DolinskiLewis-Sigler Institute for Integrative Genomics, Princeton University
Olga G TroyanskayaPrinceton University, USA Lewis-Sigler Institute for Integrative Genomics, USA Flatiron Institute, Simons Foundation
Olga G TroyanskayaPrinceton University, USA Lewis-Sigler Institute for Integrative Genomics, USA Flatiron Institute, Simons Foundation
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Datasets

ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink