Inferring dynamic regulatory programs in non-stationary expression time courses with applications to early human neural development

Comparative DNA methylomic analyses reveal insight into potential origins of novel monocyte epigenetic biomarkers of insulin resistance

Disparate anticancer activity of structurally similar multi-kinase inhibitors through cumulative differential effects on individual targets

High-throughput sequence analysis of peripheral T-cell lymphomas indicates subtype specific viral gene expression patterns and immune cell microenvironments

Gene expression study of human endometrial receptivity in IVF implantation failure patients undergoing ovarian stimulation II

Assessment of the effect of RNase A-treated Enterococcus feacalis strain EC-12(EC-12) or untreated EC-12 on transcriptome profiles in human peripheral blood mononuclear cells

Single-cell profiling of cutaneous T-cell lymphoma after treatment with vorinostat and photophoresis.

Contribution of differential cell-specific methylation to schizophrenia [RNA-seq]

Integrative vascular endothelial cell genomics identify AIDA as a coronary artery disease candidate gene (ATACseq)

Integrative vascular endothelial cell genomics identify AIDA as a coronary artery disease candidate gene (ChIPseq)

Integrative vascular endothelial cell genomics identify AIDA as a coronary artery disease candidate gene (RNAseq)

Integrative vascular endothelial cell genomics identify AIDA as a coronary artery disease candidate gene (Hi-C)

Integrative vascular endothelial cell genomics identify AIDA as a coronary artery disease candidate gene

Pioneer factor-nucleosome binding events during differentiation are motif-encoded

RNA-seq of human normal lung and lung cancer tissue

Gene expression of hiPSC-derived DA Neurons harboring SNCA A53T mutation or genome Corrected and hESC-derived WT DA Neurons and SNCA A53T mutation introduced Corrected

Genome-wide expression analysis of EPCAM+ epithelial cells from 3-dimensional lung organoids harboring Hermansky-Pudlak Syndrome-associated mutations

Genome-wide profiling at single-nucleotide resolution of brain cell types in schizophrenia [WGBS]

Genome-wide sequencing of schizophrenia and control individuals [WGS]

Contribution of differential cell-specific methylation to schizophrenia