This article explores how single-cell multiomics and spatial transcriptomics are illuminating early pregnancy, uncovering ...

Parse Biosciences and Codebreaker Labs partner to apply whole transcriptome single cell profiling and causal genomics at scale: Seattle Monday, December 22, 2025, 17:00 Hrs [IST] ...

Triglia discusses her research at the intersection of genetics, epigenetics, single-cell genomics and computational biology.

Announcing a new publication for Acta Materia Medica journal. Single-cell RNA sequencing (scRNA-seq) data from published datasets were obtained to investigate the expression and dysregulation of ...

Large-scale human genetics studies have shown that many risk variants for common and complex diseases sit in the non-coding ...

Over the past decades, large-scale human genetic studies have identified numerous risk genes and variants associated with complex diseases and traits.

A new editorial published in Med Research addresses the critical imbalance between rapid technological advancements and global health accessibility. The authors outline a vision for a new ...

Parse Biosciences, a leading provider of accessible and scalable single cell sequencing solutions, today announced that Tahoe Therapeutics has selected Parse’s GigaLab to generate data for its ...

Parse Biosciences launches Evercode Whole Blood Fixation to enable easy, high-quality single cell RNA-seq from blood.

The inaugural competition surprisingly awarded two $100,000 grand prizes to address challenges in defining robust benchmarks for complex biology.