Poster Session 1 — ASN Events

Poster Session 1 — ASN Events

Poster Session 1

The promoter landscape of inflammatory bowel disease (IBD). (#100)

Long noncoding RNA ZFAS1 in ribosome regulation: a riddle wrapped in a mystery inside an enigma (#101)

Complexity surrounding multiple isoforms of ANRIL in melanoma (#102)

Debina Ms Sarkar

In fetal testes SOX9 governs transcription and male-specific RNA splicing of target genes via a Sertoli cell genomic signature (#103)

Vincent R Harley

3D human genome modeling reveals impacts of lamin A mutations on genome architecture (#104)

Philippe Collas

Identifying and characterising novel epigenetic modifiers using X inactivation as a model system (#105)

Complexity surrounding multiple isoforms of ANRIL in melanoma (#106)

Debina Ms Sarkar

Impact of data resolution on three-dimensional structure inference methods (#107)

Prevalence of CYP2D6 Gene and Prostate Cancer Risk in People of Shiraz (#109)

A Histone Point Mutation Alters the Chromatin Landscape by Inhibiting a Histone K9/K36 Demethylase (#110)

Detecting pathogenic STR expansions in next-gen sequencing data (#111)

Harriet Dashnow

The Recycled Human Genome : Ubiquitous neufunctionalisation of pseudogenes via LINE1 mediated intron generation (#112)

Daniel W Thomson

Lineage-restricted transcription factors regulate genome organisation (#113)

Timothy M. Johanson

DNA METHYLATION ANALYSIS OF NEURODEVELOPMENTAL DISORDERS USING DISEASE-DISCORDANT MONOZYGOTIC TWINS (#114)

Namitha Mohandas

Targeted sequencing using advanced molecular inversion probes (MIPs) for discovery and validation in Mendelian disease trios (#115)

Polyceraty in Damara Sheep (#116)

Coralie M Reich

Mirror images of common, challenging and clinically relevant genetic variants provide spike-in controls for genome sequencing (#117)

The Cardiomyocyte RNA-Binding Proteome: Links to Intermediary Metabolism and Heart Disease (#118)

In planta determination of the mRNA-binding proteome of Arabidopsis etiolated seedlings (#119)

A functional genomic approach to identify new synaptic genes and drug targets to prevent neurodegeneration. (#120)

Chromatin-associated protein regulates haematopoietic stem and progenitor cell activity (#122)

Investigating the role of histone acetylation in angiogenesis (#123)

Short repeats of consecutive guanines provide transcript-specific regulation of the Polycomb repressive complex 2 (PRC2) (#124)

Chen Davidovich

Dynamic and heterogeneous DNA methylation in pluripotent cells (#125)

PacBio sequencing, de novo assembly and haplotype phasing of diploid yeast strains (#126)

Richard J Edwards

Investigating the evolution of new biochemical pathways in baker’s yeast Saccharomyces cerevisiae (#127)

Åsa Pérez-Bercoff

ASSET (antisense Set7 transcript) is regulated by oxidant redox signaling (#128)

Nazanin Karimnia

Chromatin modification in somatic cell reprogramming (#129)

Natasha Zamudio

An in silico approach to identify novel treatment options for patients with drug-resistant tuberculosis (#130)

Browning of adipose tissue in mice lacking Krüppel-like factor 3 (KLF3) (#131)

Alexander J Knights

The search for disease severity modifiers in patients suffering from blood disorders (#132)

Elizabeth S Stout

Conserved Transcriptional Architecture of Pain (#133)

Investigating the roles of KLF, SOX6 and CtBP in regulating globin gene expression (#134)

Introducing a beneficial gain of function mutation suggests a potential gene therapeutic approach for treating β‑haemoglobinopathies (#135)

Epigenomics of Rett Syndrome: the other layer of the story (#136)

Dulce B Vargas Landin

Alterations of DNA methylation and gene expression detected in the human dilated cardiomyopathy patient samples (#137)

Significant numbers of disease-associated SNPs are positioned in introns implicating their functional relevance (#138)

Ellis-van Creveld syndrome: Mutation in EFCAB7 changes the EFCAB7-EVC2 interaction in Hedgehog signaling regulation. (#139)

Tran Quynh Nhu Nguyen

Towards Personalized Medicine: Using Bayesian Methods in Genome-enabled Prediction of Complex Human Diseases (#140)

Analysis of WGS data derived from five paired primary and relapsed acute myeloid leukemia patients (#141)

Assessing the role of functional domains of a family of zinc finger transcription factors in in vivo target specificity (#143)

Wooi Fang (Catheryn) Lim

Investigating the KAT6A/B histone lysine acetyltransferase (KAT) complex (#144)

Sophia Ying Yii Mah

Structural Variant Detection in Individuals and Populations with the PacBio Sequel System (#146)

The essential function of FBP/KSRP proteins in development: Drosophila Psi interacts with Mediator to modulate MYC transcription and tissue growth (#147)

DNA methylation and transcription factor binding (#148)

propr: A Software Package for Identifying Proportionally Abundant Features using Compositional Data Analysis (#150)

ADAR1 dual function as RNA editing and potential DNA binding enzyme in the activity-dependent regulation of adaptive behaviour in the mouse (#151)

The role of neuronal specific splice factor, RBFOX1, in regulating circular RNA formation (#152)

Akira Gokoolparsadh

The ENCODE Gene Set Hub (#153)

Characterization of the genes specifically expressed in liver progenitor cells of in vitro hepatic differentiation model (#154)

The histone acetyltransferase KAT6B is essential for cortex development and the maintenance of adult neural stem cells (#156)

Maria I Bergamasco

Examining the conservation of chromatin domains between cell lineages of the same individual (#157)

A mutation in FGF9 identified in 46,XY Sex Reversal (#158)

DYSREGULATION OF SRY IN THE MALE BRAIN: A GENETIC BASIS FOR SEX BIAS IN NEUROLOGICAL DISORDERS? (#159)

Identification and characterization of ncRNAs associated with chromatin in pluripotency (#160)

Alessandro Bonetti

Alternative splicing coupled with nonsense mediated mRNA decay contributes to thermal induction of floral transition. (#162)

Sureshkumar Balasubramanian

Genomic prediction of coronary heart disease (#163)

HOME: A HISTOGRAM BASED MACHINE LEARNING APPROACH TO IDENTIFY DIFFRENTIALLY METHYLATED REGIONS IN A GENOME (#164)

Akanksha Srivastava

Identifying novel genes from integrated SOX9 knockout RNAseq/SOX9 ChIPseq datasets (#165)

Reducing the search space for causal genetic variants in sequenced pedigrees with VASP (#166)

High temporal resolution of gene expression dynamics in developing mouse embryonic stem cells (#167)

The mechanisms of alternative 3'UTRs in the control of gene expression (#168)

NetRep: a scalable permutation approach for assessing replication and preservation of network modules in large datasets (#169)

Scott C Ritchie

Mechanistic Insight into the Epigenetic Regulator SMCHD1 and its Implication in Diseases (#170)

Global down-regulation of cellular communication components is a master hallmark of cancer. (#171)

Deciphering novel transcriptional roles for Argonaute proteins in Drosophila development (#172)

IQSEC2; when two Xs are not better than one. (#173)

Cheryl Shoubridge

Identifying synthetic lethal drugs for cohesin mutant AML (#174)

Homeodomain-interacting protein kinase 1 (HPK-1) regulates stress responses and aging in C. elegans (#175)

Hannah R Nicholas

BLM and SLX4 play opposing roles in break-induced replication at human telomeres (#176)

Alexander P Sobinoff

Investigating the Role of SET-32 and SET-25 in Transgenerational Epigenetic Inheritance in C. elegans (#177)

Rachel Woodhouse

Scaffolding and completing genome assemblies in real-time with nanopore sequencing (#178)

HDAC inhibitor mediated promoter histone deacetylation differs in healthy versus diabetic individuals. (#179)

Identifying nonlinear RNAs from single-molecule CAGEscan data (#181)

From Servant to Master: the Ribosome’s instructive role in cell fate determination (#183)

Loss of RMI2 destabilises the BLM complex in Bloom-like syndrome (#184)

Novel antisense therapy for multiple sclerosis (#185)

Genome-wide analysis of allelic expression imbalance detects cis-regulatory effect of breast cancer causal SNPs identified by OncoArray project (#186)

Mahdi Moradi Marjaneh

Klf1 mutations in the second linker cause congenital non-spherocytic hemolytic anemia due to global reduction of in vivo DNA-binding affinity (#187)

F28D1.2 influences meiosis to maintain germline chromosomal integrity in Caenorhabditis elegans (#188)

An epigenomic view of seed germination in Arabidopsis thaliana (#189)

RNA processing regulates megakaryocytes and platelet production (#190)

Nucleosome positioning as a potential driver of transcriptomic alterations in prostate cancer (#191)

Methylome profiling in prostate cancer cells following radiotherapy (#192)

Kate Brettingham-Moore

Mechanism of UBE3A silencing by an antisense transcript (#193)

Ingrid Macindoe

Ultra-high quality DNA synthesis improves representation and fidelity in pooled CRISPR libraries (#194)

Daniele Belluoccio

Hippocampal Transcriptional Networks Altered By Dehydration In Mice (#195)

Identification of novel epigenetic regulators of lung development (#196)

A Multi-omics Study to Identify Biomarkers of Retinoblastoma (#197)

Daniele Belluoccio