High-throughput semi-quantitative analysis of insertional mutations in heterogeneous tumors

The inactive X chromosome adopts a unique three-dimensional conformation that is dependent on Xist RNA.

Architectural protein subclasses shape 3-D organization of genomes during lineage commitment

Clonal expansion analysis of transposon insertions by high-throughput sequencing identifies candidate cancer genes in a PiggyBac mutagenesis screen

Supression of genetic recombination in the pseudoautosomal region and at subtelomeres in mice with a hypomorphic spo11 allele

Long-range joining of intra-chromosomal DNA double-strand breaks

The Prion Protein (PrP) is involved in translation via RNA granule-like mRNPs, a connection which is impaired during neurodegenerative diseases

Integrated genome and transcriptome sequencing from the same cell

Genome Wide Characterization of Genome Organization in Mouse ES cells

Extrachromosomal DNA (microDNA) in Human, Mouse and Chicken

Mutations in histone and other genes in MLL2-impaired human and mouse cells

Humanized PRDM9 Mouse Testis H3K4me3 and DMC1 ChIP-seq

Single Cell DNA Methylome Sequencing of Human Preimplantation Embryos

Whole genome sequencing of murine derived intestinal tumour organoids

AICDA-induced epigenetic plasticity accelerates germinal center-derived lymphomagenesis

Distinct cellular mechanisms underlie anti-CTLA-4 and anti-PD-1 checkpoint blockade [WES]

Upregulation of FOXD1 by YAP alleviates senescence and osteoarthritis

Whole exome sequencing analyzed the off-target effect of gene editing through BE3 system.

The effects of H3.3K27M mutation on developing mouse brain and cooperation with Trp53 on enhancing tumorigenesis in the genetic model of H3.3K27M [Exome-Seq]

Identification of a T-cell lymphoma in plkcGAPDH transgenic mice (Exome)