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] ...
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 ...
Triglia discusses her research at the intersection of genetics, epigenetics, single-cell genomics and computational biology.
Over the past decades, large-scale human genetic studies have identified numerous risk genes and variants associated with complex diseases and traits.
Large-scale human genetics studies have shown that many risk variants for common and complex diseases sit in the non-coding ...
Dissociating tissues into single cells is a core laboratory technique and vital for widely used applications such as next-generation sequencing or flow cytometry. Scientists who employ tissue ...
The inaugural competition surprisingly awarded two $100,000 grand prizes to address challenges in defining robust benchmarks for complex biology.
Parse Biosciences launches Evercode Whole Blood Fixation to enable easy, high-quality single cell RNA-seq from blood.
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