B lymphocytes signature is associated with the success of minimization therapy in kidney transplantation

The COLCATS study: Identification of an anti-apoptotic druggable target signature for the treatment of colorectal cancer

Transcriptional and Behavioral Responses of Zebrafish Larvae to Microcystin-LR Exposure

Neuroblastoma cells depend on HDAC11 for mitotic cell cycle progression and survival

Comparison of whole-genome bisulfite sequencing library preparation strategies identifies sources of biases affecting DNA methylation data

SC3-consensus clustering of single cell RNA-Seq data

Converting adult pancreatic α-cells into β-cells by targeting Dnmt1 and Arx

Germline- and soma-specific heritable epigenetic silencing at an endogenous locus (small RNA-Seq)

Germline- and soma-specific heritable epigenetic silencing at an endogenous locus (RNA-Seq)

Germline- and soma-specific heritable epigenetic silencing at an endogenous locus

CD95/Fas increases stemness in cancer cells by inducing a STAT1 dependent Type I interferon response [array]

CD95/Fas increases stemness in cancer cells by inducing a STAT1 dependent Type I interferon response [ChIP-seq]

CD95/Fas increases stemness in cancer cells by inducing a STAT1 dependent Type I interferon response

ZSCAN5B and its primate-specific paralogs bind RNA polymerase III genes and extra-TFIIIC (ETC) sites to modulate mitotic progression [SiRNA RNA-Seq data set]

ZSCAN5B and its primate-specific paralogs bind RNA polymerase III genes and extra-TFIIIC (ETC) sites to modulate mitotic progression [Human cell line ChIP-Seq data set]

ZSCAN5B and its primate-specific paralogs bind RNA polymerase III genes and extra-TFIIIC (ETC) sites to modulate mitotic progression [Mouse Placenta ChIP-Seq data set]

ZSCAN5B and its primate-specific paralogs bind RNA polymerase III genes and extra-TFIIIC (ETC) sites to modulate mitotic progression

Transcriptome of iPSC-derived Cerebral Organoids with Heterozygous Knockout in CHD8

Mining the microbiome for modulatory effects on the murine intestinal transcriptome

Diverse interventions that extend mouse lifespan suppress shared age-associated epigenetic changes at critical gene regulatory regions (RNA-Seq)