Monday, 12th February
39th Annual Lorne Genome Conference 2018
Days
Sunday, 11th February
Monday, 12th February
Tuesday, 13th February
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Speakers
Breakfast Workshop - Implementing CRISPR CAS9
7:30AM - 8:30AM
Monday, 12th February
Auditorium
Chair: Paul Thomas
Micro Break
8:30AM - 8:40AM
Monday, 12th February
Auditorium Foyer
Session 2: Computational Biology
8:40AM - 10:10AM
Monday, 12th February
Auditorium
Chairs: Alicia Oshlack & Gaetan Burgio
Sponsored by:
Editing wild populations: local gene drive, evolutionary stability, and community guidance
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Kevin Esvelt
Conservation of transcriptional variation across human, mouse and … armadillo?!
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Sara Ballouz
Accounting for systematic bias in bulk and single cell RNA-Seq data
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Rafael Irizarry
Morning Tea
10:10AM - 11:00AM
Monday, 12th February
Exhibition Hall
Session 3: Gene Regulation
11:00AM - 12:30PM
Monday, 12th February
Auditorium
Chairs: Alistair Forrest & Leonie Quinn
Sponsored by:
Single-cell tumor transcriptomics: algorithms and applications
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Shyam Prabhakar
Transcriptional regulation of neuronal function by the histone demethylase KDM5
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Julie Secombe
Chromatin modifiers SET-32 and SET-25 establish a transgenerational silencing signal in
Caenorhabditis elegans
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Rachel Woodhouse
DNA replication timing shapes the cancer epigenome
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Qian Du
Lunch
12:30PM - 1:15PM
Monday, 12th February
Exhibition Hall
Afternoon Break/High-content functional genomics workshop
1:15PM - 2:45PM
Monday, 12th February
Horizons Room
Chair: Kaylene Simpson
Micro Break
2:45PM - 3:00PM
Monday, 12th February
Auditorium Foyer
Session 4A: Regulation of Gene Expression
3:00PM - 4:00PM
Monday, 12th February
Auditorium
Chairs: Alyson Ashe & Greg Neely
3’-deoxyadenosine induces bulk transcript lengthening via alternative polyadenylation
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Belinda J Goldie
Intron retention: A widespread and conserved mechanism of gene expression control regulated by epigenetic changes
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Justin JL Wong
Understanding the role of eosinophils in adipose tissue energy expenditure
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Kate GR Quinlan
Modelling breast cancer progression using massively-parallel single-cell RNAseq technology.
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David Gallego Ortega
Session 4B: Disease & Development
3:00PM - 4:00PM
Monday, 12th February
Horizons Room
Chairs: Andrew Perkins & Julia Horsfield
Genome sequencing of 15,000 healthy elderly Australians
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Paul Lacaze
Identifying the cause and function of T>G mutations in oesophagus and gastric cancer genomes
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Jayne A Barbour
Cardiac directed differentiation using small molecule Wnt modulation at single-cell resolution
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Nathan Palpant
Essential roles for minor class splicing in development and cancer
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Karen Doggett
Mini Break
4:00PM - 4:30PM
Monday, 12th February
Auditorium Foyer
Session 5: Julian Wells Medal/Noncoding RNA and RNA Regulation
4:30PM - 6:30PM
Monday, 12th February
Auditorium
Chairs: Vincent Harley & Timothy Mercer
Sponsored by:
MicroRNAs act on and within regulatory networks
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Greg Goodall
Coordination of RNA Processing events in vivo
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Karla Neugebauer
Enhancing the spatiotemporal sub-nuclear sequestration of RNA binding proteins by manipulating paraspeckle size
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Archa Fox
Elevated foetal globin caused by natural regulatory mutations that disrupt foetal repressor binding
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Gabriella E Martyn
Cross-regulation between the ethylene and abscisic acid hormone signalling pathways is regulated by EDF transcription factors
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Mathew G. Lewsey
RNA-dependent epigenetic silencing directs transcriptional down regulation caused by intronic repeat expansions
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Sureshkumar Balasubramanian
Duplication and deletion of key
SOX9
enhancers causes sex reversal in humans
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Brittany Croft
Canonical PRC2 function is essential for mammary gland development and affects chromatin compaction in mammary organoids
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Ewa M Michalak
Welcome to the macrogenomics era: a long read revolution
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Martin Smith
Dinner Break
6:30PM - 8:30PM
Monday, 12th February
Poster Session 2
8:30PM - 10:30PM
Monday, 12th February
Louttit Bay Room
Molecular and cellular role of RNA-binding proteins in cardiac biology and disease
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Lithin Louis
FANCM protects telomeres from aberrant replication fork processing in cancers engaging in Alternative Lengthening of Telomeres (ALT)
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Robert Lu
Investigating the role of ZBTB7A homodimerisation in adult erythroid cells
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Lana C Ly
KLF1 is a pioneer transcription factor for erythroid cells
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Graham W Magor
Restoring Central Inhibition Relieves Chronic Neuropathic Pain
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John Manion
When is a global repressor not a repressor? Genome-wide profiling of the Snail family transcription factor Worniu in neural stem cells
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Owen J Marshall
Modelling transcriptional variability in single cell RNA-seq data during human embryogenesis captures changes in the regulation of critical developmental genes
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Elizabeth A Mason
Coordinated up-regulation of splicing machinery components in a zebrafish intestinal development mutant harbouring a mutation in
gtf2h4
, a component of the general transcription factor complex, TFIIH
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Stephen Mieruszynski
Identification of Hippo pathway target genes important for tissue growth.
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Katrina A Mitchell
Genetic and chemical approaches to inhibiting hyperplasia in a zebrafish model of hepatocellular carcinoma
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Kimberly Morgan
NEAT1 changes imatinib response and contributes to tyrosine kinase inhibitor-based resistance in a chronic myleoid leukemia cell line
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Zeynep MUTLU
Whole genome dissection of the box jellyfish venom death pathway
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Greg Neely
Topoisomerase 2A is essential for maintenance of mitotic chromosome structure
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Christian Friberg F Nielsen
Investigating the evolution of truffle-like fungi
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Andy R Nilsen
Mutational Landscape of Familial Breast Cancers
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Katia Nones
Single-cell RNA profiling reveals developmental lineage relationships between the mouse mammary epithelial cells
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Bhupinder Pal
Genomics of malignant pleural mesothelioma
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Ann-Marie Patch
Human
SRY
regulates haploid specific Protamine (
PRM1
) promoter activity
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Deepali Pathak
Predicting the outcome of breast cancer using novel RNA-Seq analysis
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Andrew Pattison
Computational modeling reveals 4D genome reorganization during stem cell differentiation
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Jonas Paulsen
A Functional Genomic Approach to Identifying New Motor Neuron Disease Genes and Drug Targets
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Jodie Pearlman
A general framework for evaluating cross-platform concordance in genomic studies
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Timothy J Peters
Developing CRISPR-Cas9 Based Gene Drives in
Mus musculus
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Chandran Pfitzner
Insights into the biogenesis and possible functions of exonic circular RNA
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Chikako Ragan
The identification of rare variants in Tasmanian prostate cancer pedigrees using whole-genome sequencing
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Kelsie Raspin
Splicing factors as novel regulators of oncogenic miRNAs
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Madara Ratnadiwakara
Expanding the RNA-guided endonuclease toolkit for mouse genome editing.
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Louise Robertson
The A/HeJ Mouse: Dysfunction in Sex Development
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Jessica Robinson
MASTL overexpression promotes chromosome instability and metastasis in breast cancer
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Samuel Rogers
Overcoming off target effects in CRISPR and RNAi loss of function screens
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Joseph Rosenbluh
Characterising Human Variants of the Transcription Factors NPAS3 and NPAS4 Identified in Patients with Mental Illness
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Joseph J Rossi
Modulation of higher order chromatin structures associated with virus-specific killer T cell differentiation
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Brendan Russ
Highly Parallel Concurrent Gene Expression and Iso-Seq Analysis of Single Cells
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Jafar S. Jabbari
DECENT: Differential Expression with Capture Efficiency adjustmeNT for Single-Cell RNA-seq Data
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Agus Salim
Comparative phylogenomic evidence for a novel detoxification gene family in insects
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Jack Scanlan
Breaking point: computational interrogation of structural variation in cancer
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Colin A Semple
Investigating the role of R-loops in erythroid differentiation
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Manan Shah
Developing a bioinformatics pipeline to measure changes in ribosomal RNA genes copy number in cancer
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Diksha Sharma
In vivo
targets and mechanisms of gene control during protein synthesis
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Nikolay Shirokikh
Targeting telomeric repeat-binding factor 2 (TRF2) with small molecule inhibitors to prevent cancer cell growth
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Alexander P. Sobinoff
Gene editing of the multi-copy H2A.B.3 gene family by a single pair of TALENs
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Tanya Soboleva
Investigating the role of
MYD88
mutations in lymphoma.
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Huma Sohail
BET bromodomain inhibition sensitises ribosomal DNA to localised damage and provides a robust synergistic therapeutic strategy for treating AML
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Jirawas Sornkom
Nuclear microRNAs as Direct Regulators of Transcription
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Laura Sourdin
The Search for Disease Severity Modifiers in Patients Suffering from Blood Disorders
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Elizabeth S Stout
Invasive Lobular Breast Cancer: Using tumour genome-wide DNA methylation to further subtype and aid in the identification of susceptibility genes.
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Medha Suman
Integrated profiling of single-cell chromatin accessibility and transcriptome reveals regulatory heterogeneity
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Stephanie Sun
Exploring the combinatorial effects of epigenetic modifiers upon the mammalian genome using CRISPR-dCas9
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Tessa Swain
Identifying Novel Testis-Determining Genes from Integrated RNAseq and ChIPseq Data
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Aleisha Symon
Investigating the role of Cis and Trans acting regulators in the process of X inactivation
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Andres ATdF Tapia del Fierro
Investigating DNA transposition as a cause of genomic instability and therapy-resistance in Chronic Myeloid Leukaemia
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Daniel Thomson
Bayesian neural network based modelling of steady-state splicing mechanism.
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KANUPRIYA TIWARI
Repetitive RNA and genomic instability in high-grade serous ovarian cancer progression and development
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James R Torpy
Investigation into the mechanisms of alternative 3’UTRs in the control of gene expression
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Rachael E Turner
Pre-miRNA Folding Through Context-Free Grammar Parsing and the Identification of miRNA Using a Feedforward Neural Network
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Sonika Tyagi
Click chemistry enables preclinical evaluation of targeted epigenetic therapies
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Dean S. Tyler
Characterization of
COL3A1
mutations causing Ehler-Danlos Syndrome type IV: the first step in designing molecular therapies
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Sasiwimon Utama
shRNA screen for novel epigenetic regulations of y-globin silencing
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Jim Vadolas
Novel contribution of acetylated histone variant H2A.Z in activation of neo-enhancers in prostate cancer.
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Fatima Valdes Mora
Transcriptional characterization of low input frozen brain samples at single-nucleus resolution using 10x Genomics Chromium microfluidics
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Dulce Vargas Landin
Racing against the (epigenetic) clock: physical activity reverses age-related epigenetic drift in human skeletal muscle
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Sarah Voisin
Dissecting the roles of eIF2 and eIF3 during translation using TCP-seq
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Susan Wagner
Molecular Dynamics Modelling of a Variant of Unknown Effect in RAD51D
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Matthew Wakefield
Development and optimization of an efficient method for CRISPR/Cas correction of patient-specific iPSCs
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Qi Wang
An optimal approach to assembling chloroplast genome
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Weiwen wang
Characterizing the epigenetic modifier Smchd1 in X chromosome inactivation
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Iromi Wanigasuriya
NxtIRF: A novel computational approach to measure differential intron retention in cancer databases
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Alex CH Wong
Roles of histone variant H3.3 and ATRX in tumourigenesis
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Lee Wong
Systematic discovery of coding and noncoding transcriptomic variants in liver cancer
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Hyun Goo Woo
DNA methylation and transcription factor binding
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Lu Yang
ZNF827 - a molecular target for telomere maintenance in cancer
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Sile Fiona Yang
Identification and characterization of novel cell populations using single-cell RNA-seq: an example on breast cancer T cell infiltrate
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Chengzhong Ye
The FUBP1
Drosophila
ortholog Psi interacts with the Mediator Complex to regulate growth through modulating expression of
MYC
and RNA processing machinery
-
Olga Zaytseva
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