Understanding the role of miRNA-143 (miR-143) in ischemia-induced retinopathy via RNA transcriptome profiling

Expression data of micRNA from spleen CD4+CD25+ Treg cells

Gene expression analysis on Naïve CD4 T cell with JMJD3 knockdown

Chromosome conformation capture by high thoughput sequencing (HiC) during Naïve CD4 T cell activation

H3K27me3 and JMJD3 ChIP-seq during naïve CD4 T cell activation

Generation Sequencing Facilitates Quantitative Analysis of Wild Type and AGC1-4 Transcriptomes

Genome-wide analysis of m6A modification

Mapping the global chromatin connectivity network in colorectal cancer cell HCT116 and Oxaliplatin-resistant cell HCT116OxR [RNA-seq]

Mapping the global chromatin connectivity network in colorectal cancer cell HCT116 and Oxaliplatin-resistant cell HCT116OxR [Hi-C]

Mapping the global chromatin connectivity network in colorectal cancer cell HCT116 and Oxaliplatin-resistant cell HCT116OxR [ChIP-seq]

Mapping the global chromatin connectivity network in colorectal cancer cell HCT116 and Oxaliplatin-resistant cell HCT116OxR [ATAC-seq]

Mapping the global chromatin connectivity network in colorectal cancer cell HCT116 and Oxaliplatin-resistant cell HCT116OxR

RNA-Seq of LbDREB6 transgenic Populus ussuriensis

Identification of pharmacologic inhibitors and activators of IL-4-induced macrophage polarization

RNA-Seq of circHIPK3 knockdown (KD) samples in UMUC3 and J82

Cis-regulatory architecture of human ESC-derived hypothalamic neuron differentiation aids in variant-to-gene mapping of relevant common complex traits (ATAC-Seq)

Cis-regulatory architecture of human ESC-derived hypothalamic neuron differentiation aids in variant-to-gene mapping of relevant common complex traits (Capture C)

Cis-regulatory architecture of human ESC-derived hypothalamic neuron differentiation aids in variant-to-gene mapping of relevant common complex traits (RNA-Seq)

G-CSF SECRETED BY EPIGENETICALLY REPROGRAMMED MUTANT IDH1 GLIOMA STEM CELLS, REVERSES THE MYELOID CELLS'-MEDIATED IMMUNOSUPPRESSIVE TUMOR MICROENVIRONMENT [Run1736]

Isogenic human pluripotent stem cell disease models reveal actin binding Rho activating protein deficiency underlies the cardiac troponin T DK210 mutation-induced familial dilated cardiomyopathy I