A ONECUT1 regulatory, non-coding region in pancreatic development and diabetes [Nanopore-seq]

Spatially exploring RNA biology in archival formalin-fixed paraffin-embedded tissues

Gene expression responses to oxygen challenge in a panel of human brain organoids

A PLURIPOTENT STEM CELL PLATFORM FOR in VITRO SYSTEMS GENETICS STUDIES of MOUSE DEVELOPMENT

Single Nucleus DNA Sequencing of Flow Sorted Archived Frozen and Formalin Fixed Paraffin Embedded Solid Tumors

Neoantigen identification for 1956 and F244 murine MCA-sarcomas

CRISPR Screening Uncovers a Long-Range Enhancer for ONECUT1 in Pancreatic Differentiation and Links a Diabetes Risk Variant

Proteogenomics analysis to identify acquired resistance-specific alterations in melanoma PDXs on MAPKi therapy [WES]

A scalable, low cost, multi-omic interrogation and sample hashing workflow for single-cell analysis using the Seq-Well S3 platform

Mutational analysis of TLK1 and MDM1

Dysregulated innate immune signaling cooperates with RUNX1 mutations to transform an MDS-like disease to AML

Dysregulated innate immune signaling cooperates with RUNX1 mutations to transform an MDS-like disease to AML (WES)

Brd4::Nutm1 fusion gene initiates NUT carcinoma in vivo [WGS]

CRISPR Screening Uncovers a Long-Range Enhancer for ONECUT1 in Pancreatic Differentiation and Links a Diabetes Risk Variant [long_read_seq]

Whole exome sequencing of NT2.5 and NT2.5-LM cell lines

Whole-exome sequencing analysis of HNM007, AKR, and NOOC1 cells.

RNA-Seq, WGS, WXS of mouse myeloma tumors derived from Vk*MYC transgenic mice

Characterization of the mutational landscape of high-grade gliomas in a Latin American cohort

A study of genetic variants associated with skin traits in the Vietnamese population

Modeling the next-generation of rhabdomyosarcoma organoids to predict effective drug combinations [Exome panel]