- Produced ready-to-use code for bioinformatic pipelines, thereby automating the processing and ingestion of data to the data lake- Identifyed valuable public omics data sources, structured, annotated, defined schema, and automated data ingestion. Added more than 1.5 million datasets to the data lake- Developed custom analysis workflows to build consumption journeys around different biological data types- Trained interns on scRNA-seq Data Analysis and lead a curation project for manually curating single cell data for cell type on scale.

- Reviewed the disease models of closely associated Disorders of Sexual Development (DSDs), Frasier Syndrome (FS) and Wilm’s Tumor (WT1)- Investigated the genotype and phenotype relation of transcription factor Wilm’s Tumor protein 1(WT1) and the role of its isoforms on the process of Gonadal Development- Modeled the structure of +KTS/-KTS isoforms of WT1 in complex with DNA for probing differential binding affinities- Computed the differences in binding using Umbrella sampling and Steered Molecular Dynamics which validated phenotypic outcome