Characterization of the genes specifically expressed in liver progenitor cells of in vitro hepatic differentiation model Overlapping promoters and operators of Mycobacteriophage D29 ―An insight into the evolution of regulatory elements A novel kinase in the regulation of telomere integrity Common variants at 1p12, 2q34, 3q21.3, 5q14.3 and 7p11.2 are associated with Macular Telangiectasia type 2 (MacTel) The histone acetyltransferase KAT6B is essential for cortex development and the maintenance of adult neural stem cells Examining the conservation of chromatin domains between cell lineages of the same individual A mutation in FGF9 identified in 46,XY Sex Reversal Cortisol and Betamethasone activate a different yet overlapping set of glucocorticoid receptor-regulated target genes during mammalian lung development DYSREGULATION OF SRY IN THE MALE BRAIN: A GENETIC BASIS FOR SEX BIAS IN NEUROLOGICAL DISORDERS? Identification and characterization of ncRNAs associated with chromatin in pluripotency Systematic identification of functionally relevant noncoding variants in ADHD The Medical Genome Reference Bank Phase 1: Population genomics of a disease-depleted, elderly Australian population Alternative splicing coupled with nonsense mediated mRNA decay contributes to thermal induction of floral transition.  Sequence variation currently not utilised in genomic selection of NZ dairy cattle Genomic prediction of coronary heart disease HOME: A HISTOGRAM BASED MACHINE LEARNING APPROACH TO IDENTIFY DIFFRENTIALLY METHYLATED REGIONS IN A GENOME Identifying novel genes from integrated SOX9 knockout RNAseq/SOX9 ChIPseq datasets Embryonic DNA methylation remodelling in the chordate Branchiostoma lanceolatum Reducing the search space for causal genetic variants in sequenced pedigrees with VASP High temporal resolution of gene expression dynamics in developing mouse embryonic stem cells SRSF3 facilitates reprogramming and coordinates gene expression in pluripotent cells through multiple RNA processing machineries