Transcriptome of normal,paracancerous and cancerous colon tissues based on RNA-seq method

Massively parallel saturation genome editing of an essential mitochondrial targeting sequence (Tn5)

Massively parallel saturation genome editing of an essential mitochondrial targeting sequence

RNA-seq analysis of K562 cells (K562-shX) with stable integration of a tet-inducible shRNA targeting a candidate (X) transcription factor from ENCODE/HudsonAlpha-MyersLab

RNA Sequencing Analysis Generates Comprehensive Transcriptomic Landscape and Identifies PTK6 as a Novel Tumor Suppressor Gene in Esophageal Squamous Cell Carcinoma

Identification of a Novel Angiogenesis and Tumor Suppressor Gene Rab25 in Esophageal Squamous Cell Carcinoma

Melanoma short-term cultures and cell lines: expression profiling and CNV analyses

RNA-Seq of melanoma short-term cultures and cell lines

Nucleosome map of the IMR90 fibroblast cell line

TCERG1 regulates alternative splicing of Bcl-x gene by modulating the rate of RNAPII transcription

Cataloging human PRDM9 variability utilizing long-read sequencing technologies reveals PRDM9 population-specificity and two distinct groupings of related alleles

Integrative Annotation of Human Large Intergenic Non-Coding RNAs Reveals Global Properties and Specific Subclasses

K562 polyA RNA-Seq

ZNF274 colocalizes with the histone methyltransferase SETDB1 at ZNF 3' ends.

Genome-wide binding of the orphan nuclear receptor TR4 suggests its general role in fundamental biological processes

Functional analysis of Kap1 genomic recruitment

L3MBTL2 protein acts in concert with PcG protein mediated monoubiquitination of H2A to establish a repressive chromatin structure [ChIP-Seq data].

Genome-wide analysis of transcription factor E2F1 mutant proteins reveals that N- and C-terminal protein interaction domains do not participate in targeting E2F1 to the human genome.

Genetic Framework for GATA Factor Function in Vascular Biology

UCSF-UBC Human Reference Epigenome Mapping Project