Polymorphic cis- and trans-regulation of human gene expression

Effect of read-mapping biases on detecting allele-specific expression from RNA-sequencing data.

Understaning mechanisms underlying human gene expression variation with RNA sequencing

RNA-sequence analysis of human B-cells

An EMT-driven alternative splicing program occurs in human breast cancer and modulates cellular phenotype.

Ribosome footprinting in the cytosol and endoplasmic reticulum

Molecular Signature of CAID Syndrome: Noncanonical Roles of SGO1 in Regulation of TGF-β Signaling and Epigenomics.

Differential genomic targeting of the transcription factor TAL1 in alternate hematopoietic lineages

SRC-1 targets ADAM22: an ER-independent mechanism of tumour progression in endocrine resistance

H3K9/14Ac in TC-797 genome

Population genetic structure of the Ashkenazi Jewish population

Evaluation of affinity-based genome-wide DNA methylation data: effects of CpG density, amplification bias and copy number variation

Genome-wide association study on Tuberculosis in the Chinese Population

Gene Pool Preservation Across Time And Space In Mongolian-speaking Oirats [Set 1]

Gene Pool Preservation Across Time And Space In Mongolian-speaking Oirats [Set 2]

Molecular Signature of CAID Syndrome: Noncanonical Roles of SGO1 in Regulation of TGF-β Signaling and Epigenomics. [BiSulfite-seq]

Assessing the ability of various genomic features to prioritize causal non-coding variants associated with diseases and traits [MPRA]

SNP genotyping of ǂKhomani San