If your research study involves bioinformatics and genomics, we've got you covered! The Graduate School works with different providers to provide a range of sessions with esteemed providers such as QCIF.

Useful links

  • Queensland Facility for Advanced Bioinformatics (QFAB): Bioinformatics, biostatistics and biodata expertise
  • Hacky Hour (supported by RCC, QCIF, IMB and wonderful volunteer helpers!): RCC runs consultations every Tuesday at Cafe Nano. Come and ask IT questions such as: getting started with Python and R, stats, machine learning, bio-image, software tools, research data management (RDM), how to access high performance computing, cloud data storage and tools for data cleaning and data visualisation. Bring your project's IT problems or come along as a helper! Very occasionally Hacky Hour may not run; follow us on Twitter (@HackyHourStLuc​) to get the latest announcements. Aside from the usual IT research questions, 
    • First Tuesday of the monthBioinformatics Hacky Hour, ask bioinformatics analysis, software and pipeline questions
    • Last Tuesday of the monthBioLab Hacky Hour, ask about experimental design and technical sample processing questions to get started in the lab

Genome annotation with Apollo [webinar]

13 November 2024 9:00am12:30pm
Genome annotation is crucial to defining the function of genomic sequences. Apollo is a popular tool for facilitating real-time collaborative, manual curation and genome annotation editing. In this workshop we will learn how to use Apollo to refine genome annotations. Registration closes 6 November at 9am.

RNA Seq analysis using Galaxy (QCIF) [webinar]

24 October 2024 9:00am5:00pm
This practical workshop will introduce the specific skills and applications used in the analysis of RNA-Seq gene expression data.

Introduction to NGS platforms and bioinformatics analysis (QCIF) [webinar]

3 September 2024 9:00am5:00pm
This hands-on practical workshop is an introduction to next generation sequencing technologies and how they work, providers, common bioinformatics workflows, standardised file types, quality control and an introduction to Galaxy Australia.

Long-read assembly using Galaxy (QCIF) [webinar]

16 August 2024 9:00am12:30pm
Explore how long and short read data can be combined to produce a high-quality ‘finished’ bacterial genome sequence. Termed ‘hybrid assembly’, we will use read data produced from two different sequencing platforms, Illumina (short read) and Oxford Nanopore Technologies (long read), to carry out de novo genome assembly.

Single-cell RNA Seq analysis using Galaxy (QCIF) [webinar]

4 July 2024 9:00am5:00pm
This hands-on workshop will cover the basics of single-cell RNA-Seq analysis, using the Galaxy platform. Starting from a table of gene counts we will evaluate, filter, annotate and visualise the data. We will also cover clustering, cell type identification and differential expression. No prior experience with Galaxy required.