An individual’s genome is identifiable. But datasets of RNA sequences from single cells are like a blurry photocopy of the genome. The sequence numbers are small, the data are noisy, and the sequences ...
This article explores how single-cell multiomics and spatial transcriptomics are illuminating early pregnancy, uncovering ...
Research presented by Dr Erik Sahai has shown that early, reversible diversity in tumour cell state can blunt the effect of ...
Parse Biosciences launches Evercode Whole Blood Fixation to enable easy, high-quality single cell RNA-seq from blood.
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