Author

Sanchari Datta

Broad InstituteORCID 0000-0002-3613-5180Unclaimed ORCID profile · follow to get notified of new preprints

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Sanchari Datta1 paper

Biology Disciplines

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Developmental Biology· 1 Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Assay:scRNA-seq· 2 Approach:statistical model· 2 Assay:ATAC-seq· 1 Approach:Bayesian inference· 1 Research Focus:benchmarking· 1 Research Focus:database / resource· 1 Research Focus:differential expression· 1

Frequent Co-Authors

Bellis MiniD· 2 shared Benjamin M. NealeiD· 2 shared Joaquín Pérez‐SchindleriD· 2 shared Melina ClaussnitzeriD· 2 shared NIVEDITA NAMBRATH· 2 shared Wei ZhouiD· 2 shared Yi HuangiD· 2 shared Yijia Christiana LiuiD· 2 shared

Activity by Year

2020-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 44 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Bellis MinORCID

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3 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintSep 14, 2026

Scalable context-dependent single-cell eQTL mapping reveals disease-relevant regulatory variation beyond static models

Yijia Christiana Liu, Anna S. E. Cuomo, Yi Huang…·Wei Zhou

The paper introduces CASTIE, a method for context-dependent eQTL mapping in single-cell data, identifying regulatory variants missed by static models and linking them to disease traits.

1 citation

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GenomicsbioRxivPreprintAug 19, 2026

Metabolic disease-relevant stimuli unmask context-dependent genetic regulation of cardiometabolic loci in human adipocytes

Yi Huang, Joaquín Pérez‐Schindler, Sanchari Datta…·Melina Claussnitzer

The paper maps context-dependent genetic regulation of cardiometabolic loci in human adipocytes using a multi-donor cell village system and single-nucleus multiome sequencing under various metabolic stress conditions.

DOI 10.64898/2026.08.12.744187

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Developmental BiologyScientific ReportsPeer-reviewedAug 13, 2020

Diverse Species-Specific Phenotypic Consequences of Loss of Function Sorting Nexin 14 Mutations

Dale Bryant, Marian Seda, Emma Peskett…·Philip Stanier

This study examines the phenotypic effects of SNX14 loss-of-function mutations in mice and zebrafish, revealing species-specific consequences despite conserved biochemical roles.

13 citations

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