The 9th Annual Irish Next Generation Sequencing meeting will take place on 30th May 2019 in the Tercentenary Hall, Trinity Biomedical Sciences Institute (TBSI). This prestigious event provides a forum for a number of high profile speakers to outline research in all aspects of NGS, ranging from personalised medicine to data management. The meeting is aimed at anyone currently working with next-generation sequencing data, and has been structured to encourage open discussion on current technologies, their applications, associated problems and solutions. Registration is free for non-commercial attendees (please complete the form below or email 'trinseq@gmail.com' for any enquiries) and lunch will also be provided.
Programme
Printable Draft Programme/Flyer (PDF 1.083 kB)
Programme: 30th May 2019 (9.30am -5pm), Tercentenary Theatre, Trinity Biomedical Sciences Institute (TBSI) | ||
09.30 | Registration With Tea and Coffee |
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10.00 | Elaine Kenny (ELDAbiotech & TrinSeq) | What's 'NEXT' on the Horizon? Current NGS Technologies and Platforms |
10.20 |
Denise Harold (DCU) | Bioinformatics basics for NGS- How to spot the good, the bad and the ugly |
10.40 | Samuel Bouvet (Takarabio) | Most recent advents in single cell NGS to unravel biological complexity and disease |
10.55 |
David Simpson (QUB) | Molecular dissection of cell populations in culture and in vivo with scRNA-Seq |
11.15 | Simit Patel (Partek Inc) | How to make your NGS data analysis simple |
11.30 | Dan Hurley (UCD) | Bioinformatic approaches to rapidly screen >188,000 Salmonella WGS datasets during Irish dairy contamination event |
11.50 |
Yanxiang Zhou (Illumina Ventures) | Funding innovation in genomics and personalised health- A VC’s Perspective |
12.00 | Lunch | |
13.00 | Arun Decano (DCU) | The origin, evolution and population structure of 4,071 Escherichia coli ST131 genomes |
13.20 | Stephen Hague (10X Genomics) | 10X Genomics, Multi-Omic Applications |
13.35 |
Paul Smith (Teagasc) | Amplicon Sequencing - The Positives Of Being A Control Freak |
13.55 | Alex Stretton (Agilent) | Next Generation Sequencing with Agilent |
14.10 | Brenda McManus (TCD) | Characterisation of novel Arginine Catabolic Mobile Elements (ACMEs) in subgingival Staphylococcus epidermidis elucidated by short read and long-read whole genome sequencing |
14.30 | ||
14.50 | Tea & Coffee | |
15.20 | Naomi Walsh (DCU) | Transcriptomic characterisation of 3D organoid models to study pancreatic cancer development and progression |
15.40 | Gyongyi Lukacs (Biosciences) | What’s new in NGS from ThermoFisher Scientific: Collibri Stranded RNA Library Prep Kit for Illumina |
15.55 | Bruce Moran (UCD/SVUH) | Clinical benefits of sequencing rare cancer cases |
16.15 | Brennan Martin (Qiagen) | QIAseq FastSelect: Novel Method for rRNA and Globin Removal |
16.30 | Kathleen Gorman (CUH) | NGS in Paediatric Neurology - Impact on patient care |
16.50 | Elaine Kenny | Closing Remarks |