Blog Archives

Genomewide paired DNA-RNAseq analyses to discover intronic splice mutation hotspots in neurological disorders.

Oncogenic reactivation of young L1s is a hallmark of colon cancer.

A comprehensive catalog of 3D genome organization in diverse human genomes facilitates understanding of the impact of structural variation on chromatin structure.

The Interplay between Mutagenesis and Extrachromosomal DNA Shapes Urothelial Cancer Evolution.

Phospho-seq: Integrated, multi-modal profiling of intracellular protein dynamics in single cells.

The First Insight into the Hereditary Fusion Gene Landscape of Amyotrophic Lateral Sclerosis.