Sunday, 12th February 44th Lorne Genome Conference 2023
Registration Desk Open
12:00PM - 6:00PM
Sunday, 12th February
Lobby
Welcome and Acknowledgement of Country
1:45PM - 2:00PM
Sunday, 12th February
Heritage Ballroom
Chair: Marnie Blewitt
Session 1: Regulation of gene expression
2:00PM - 3:10PM
Sunday, 12th February
Heritage Ballroom
Chairs: Kate Quinlan & Greg Neely
Sponsored by:
Afternoon Tea / Hotel Check-in
3:10PM - 3:50PM
Sunday, 12th February
Convention Centre
Session 2: Comparative and Population genomics
3:50PM - 5:00PM
Sunday, 12th February
Heritage Ballroom
Chairs: Michael Clark & Emily Wong
Mid-Career Award Presentations (Millenium Prizes)
5:00PM - 6:00PM
Sunday, 12th February
Heritage Ballroom
Chairs: Peter Boag & Archa Fox
Sponsored by:
Trade mixer (Exhibitors and Lab Heads Only)
6:00PM - 7:00PM
Sunday, 12th February
Convention Centre
Welcome Function
7:00PM - 8:30PM
Sunday, 12th February
Lorne Common (Footy Oval)
Poster Session 1
8:30PM - 10:00PM
Sunday, 12th February
Convention Centre
- Whither the sex chromosome: the fate of sex chromosomes during the evolution of monoicy from dioicy in liverworts - John Bowman
- Spatial lncRNA signatures in colorectal cancer - Holly R Pinkney
- Three-dimensional chromatin organisation shapes origin activation and replication fork directionality - Kate Giles
- LINE-1 activity in mammalian primordial germ cell specification - Renee R. Chu
- Cordycepin induces widespread mRNA 3'UTR lengthening - Rachael E Turner
- Genome wide CRISPR screen identifies SAMHD1 and translation initiation factors, eIF4A1 and eIF4G1 as genes involved in the regulation of replication stress induced mitotic cell death - Aisling O'Connor
- The Human Dendritic Cell Atlas: An Integrated Transcriptional Tool to Study Human Dendritic Cell Biology - Zahra Elahi
- JBrowse 2: A modular genome browser with views of synteny and structural variation - Ian Holmes
- A nucleosomal DNA-interacting surface in EZH2 is required for the canonical function of PRC2 - Qi Zhang
- Uncovering Drug-Protein and Protein-Protein Interactions with Deep Mutational Scanning - Matthew J Wakefield
- Ligation derived artefacts can cloud somatic recombination event calling using nanopore sequencing - Nathan Smits
- The three-dimensional structure of chromatin condensed by PRC1-CBX8 is porous and stabilized by dynamic multivalent interactions - Xiao Han Ng
- A comprehensive investigation of genomic variants in Prostate Cancer reveals 30 regulatory variants with possible functional impact - Mahdieh Labani
- Distinct modes of telomere synthesis and mitotic telomere lengthening in cancers engaging in Alternative Lengthening of Telomeres - Robert Lu
- CRISPR-gene editing in haematopoietic stem and progenitor cells: modelling and therapy for telomere biology disorders - Chen (Ashley) Yang
- A mechanism of mitotic telomere deprotection - Ronnie Ren Jie Low
- Discovering the influence of an enriched environment on neuronal epigenome ageing as a potential strategy for treating age-related diseases. - Bao Ngoc Tran
- Post-transcriptional regulation of fungal cell walls by the conserved RNA-binding virulence factor Ssd1 - Marah Jnied
- A uniquely prevalent deleterious variant within POMC gene leading to obesity in Estonian Biobank cohort - Erik Abner
- MisMatchFinder: Detection of somatic mutation signatures from low coverage WGS - Sebastian Hollizeck
- Nuclear F-actin and the DNA damage response regulate telomerase recruitment in cancer cells - Ashley Harman
- Eyes absent family members EYA4 and EYA1 promote the kinase activity and mitotic function of PLK1 through dephosphorylation of pY445 - Christopher B Nelson
- Disparities in spatially variable gene calling highlight the need for benchmarking spatial transcriptomics methods. - Natalie C Charitakis
- FUBP1/Psi function in the niche is essential to prevent neural stem cell overproliferation - Damien Muckle
- Controlling translation initiation is key to successful recombinant protein production - Chun Shen Lim
- Subclass II bHLHs are a key regulator in the ancestral function of spore wall deposition in land plants - Jonathan Levins
- Finding treatments for chromatin disorders: early postnatal interventions to improve neurodevelopmental outcomes - Hannah K Vanyai
- Inhibition of retinoic acid signaling impairs cranial and spinal neural tube closure in mice lacking the Grainyhead-like 3 transcription factor - Zihao Deng
- Integrative analysis reveals marker genes for intestinal mucosa barrier repairing in clinical patients - Zihao Deng
- Intronic FTO deletions lead to IRX3 oncogene activation through enhancer hijack in T cell acute lymphoblastic leukaemia - Sunniyat Rahman
- Genomic comparison of primary dermal melanoma (PDM) and subcutaneous metastatic melanoma (SCM) - Peinan Zhao
- ResTORing bone growth - investigating mTORC1 activation during perinatal catch-up growth of mouse limbs - Shanika L. Amarasinghe
- A method for stabilising the XX karyotype in female mESC cultures - Andrew Keniry
- The functional domains of the KLF transcription factor family may contribute to their different in vivo genomic localisation - Manan Shah
- Discovery of novel neuropsychiatric disorder risk gene transcripts in human brain - Ricardo De Paoli-Iseppi
- Effects of loss of the Börjeson–Forssman–Lehmann syndrome gene Phf6 on brain development - Melody PY Leong
- Nanopore direct RNA sequencing reveals insight into the transcriptome and epitranscriptome of human brain - Josie Gleeson
- The role of class II KNOX and BELL TALE-class homeodomain genes in Marchantia polymorpha sporophyte development - Tom Dierschke
- Adipose tissue-resident eosinophils are transcriptionally distinct from blood eosinophils: harnessing this knowledge to uncover anti-obesity targets - Kate Quinlan
- A deep learning model for accurate identification of RNA modification sites - Korawich Uthayopas
- GATA1 binding in the beta globin locus: at the mercy of DNA methylation? - Sonia Goozee
- Identification of cell barcodes from long-read sc-RNAseq with BLAZE - Sefi D.J Prawer
- Progesterone receptor cooperates with RUNX1 and promotes chromatin accessibility to activate gene expression in ovarian granulosa cells during ovulation - Thao Dinh
- PRIMITI: A machine learning model for accurate prediction of miRNA target identification - Korawich Uthayopas
- Transcriptome-wide analysis of the closed-loop model of translation - Yu-Ting Hung
- Analyzing neuronal images of amyotrophic lateral sclerosis (ALS) disease derived from induced pluripotent stem cell (iPSC) - Deshani Geethika Poddenige
- DNA methylation directs repression of γ-globin through the MBD2-NuRD complex in haemoglobin switching - Henry W Bell
- Interpretable machine learning for identifying electrophysiological indicators of ALS using intracellular and extracellular recordings from iPSC-derived neurons - Nisal Ranasinghe
- Mapping histone modifications in fetal and adult-like red blood cells - Michael O'Dea
- Investigation of the candidate sex determination gene AMHY in monotremes - Frank Grutzner
- Amino acid availability regulates tumour immune escape through alternative polyadenylation of MHC class I - Keziah E Ting
- Divergence in genome structure and function underpinning root systems in legumes - Ying Sun
- discoAnt – A novel workflow for the identification and quantification of transcript isoforms from long-read amplicon sequencing - Shweta S Joshi
- Evaluating the direct and indirect effects of SARS-CoV-2 on multiple organ systems using stem cell-derived human tissue - Michael See
- Paediatric glioma histone H3.3 K27M/G34R mutations drive abnormalities in PML Nuclear Bodies - Hsiao P J Voon
- Maternal adipose tissue DNA methylation and gene expression associated with excessive gestational weight gain - Yen Ting Wong
- Most Australian stem cell lines are not formally registered - Mengqi Hu
- Utilizing a “four core genotypes” rat model to investigate sex differences in human disease - Shanie Landen
- Exploitation of the UDP-glucose hydrolase NUDT22 as novel target in cancer therapy - Melanie Walter
- The L1-Cre Reporter System: Circumventing Engineered LINE-1 Retrotransposon Silencing - Alexander L. Carleton
- Notch is required in the niche to control neural stem cell fate - Tanya Javaid
- The lack of NSUN2 RNA methyltransferase affects the role of UPF1 RBP - Marco Guarnacci
- Dissecting the role of RNA-DNA hybrids in DNA damage and repair - Attila Horvath
- Investigating a postnatal treatment for Prader-Willi Syndrome: Switching on maternally imprinted genes by targeting the epigenetic repressor SMCHD1 - Tamara Beck
- Variable number tandem repeat (VNTR) allele genotype of an SVA retrotransposon correlates with differential gene expression at the MAPT locus - Alexander Fröhlich
- Characterization of a novel Transcriptional Start Site in human myeloid cells that generates unique NRG1 isoforms - Miguel MAB Berrocal
- Glucocorticoid signalling via the glucocorticoid receptor regulates primary cilia length and structure in the fetal mouse renal tubule - Jianshen JL Lao
- The effect of longevity interventions on the aging epigenome - Jack Harley