Mapping microglia diversity in the human brain through the integration of high-dimensional techniques

scRNA-seq for analyzing the characteristics of PBMC in patients with autoimmune hepatitis

cGAS/STING drives ageing-related inflammation and neurodegeneration

DNA damage contributes to neurotoxic inflammation in Aicardi-Goutières Syndrome astrocytes [scRNA-Seq]

DNA damage contributes to neurotoxic inflammation in Aicardi-Goutières Syndrome astrocytes

The Fc receptor CD32 identifies primed human hemogenic endothelial cells [scRNA-seq]

CD32 captures committed haemogenic endothelial cells during human embryonic development.

A novel STING variant triggers endothelial toxicity and SAVI disease

Single-cell transcriptome analysis revealed continuous changes in molecular phenotypes during epithelial-to-mesenchymal transition

RNA-seq based transcriptome profiles of the human testis tissues across multiple conditions, with an intention to mainly study non-obstructive azoospermia

Three-dimensional disorganisation of the cancer genome occurs coincident with long range genetic and epigenetic alterations [RNA-seq]

Epigenetic reprogramming at estrogen-receptor binding sites alters the 3D chromatin landscape in endocrine resistant breast cancer [RNA-seq]

Next generation sequencing transcriptome analysis of patient-derived macrophages after SARS-CoV-2 mRNA vaccination

Interleukin-11 signaling drives vascular smooth muscle phenotypic switching and contributes to aortic remodelling

DNA-PKcs is a key transcriptional and splicing regulator of AR-Vs in advanced prostate cancer

Improving prime editing with an endogenous small RNA-binding protein

Overexpression of the cytokinesis regulator PRC1 activates the p53 pathway due to cytoplasmic microtubule-bundling resulting in senescence of A549 lung cancer cells

Inhibition of SWI/SNF broadly disrupts enhancers and reveals remodeler redundancy at promoters

Splicing modulators impair DNA damage response and induce killing of cohesin-mutant MDS/AML

Leveraging the Epigenomic Landscape to identify Histology-Specific Master transcription factors and to functionally annotate risk loci in renal cell carcinoma