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This hands-on workshop is designed for HDRs and Staff at QUT with no command line or bioinformatics experience and for those with Bioinformatics skills interested in running reproducible, scalable, and portable Nextflow pipelines for variant calling and metagenomics analyses. The workshops will allow participants to use and run bioinformatics pipelines using basic command line skills and Jupyter Notebooks.

Date: 7th May - 4th June 2024

Venue: GP S506

Short URL link:

https://eresearchqut.atlassian.net/l/cp/WU1ru1e0

HPC Account

The first session is all about using the HPC. You will need a HPC account to take part in the session. If you do not have one, please request one here.

Brief Survey 

 Fill a short survey by Monday 6 May 2024. Alternatively, scan the following QR code to access the survey:

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Workshop Sessions

Five workshop sessions will introduce participants to using QUT’s HPC, running bioinformatics pipelines for variant calling and metagenomics analyses. Find below information on individual sessions. In case you have not yet registered for all sessions of interest, feel free to register using the direct UniHub links below:

Session

Description

Date

Time

Location

UniHub

1

Bioinformatics - Introduction to the HPC and basic Unix commands

7 May

9.00 am – 12.00 noon

GP-S-506

N/A

2

Bioinformatics - Variant calling data analysis using Illumina datasets

14 May

9.00 am – 12.00 noon

GP-S-506

Book

3

Bioinformatics - Variant calling using Oxford Nanopore data

21 May

9.00 am – 12.00 noon

GP-S-506

Book

4

Bioinformatics - Introduction to metagenomics using Illumina data

28 May

9.00 am – 12.00 noon

GP-S-506

Book

5

Bioinformatics - Metagenomics using Nanopore and downstream analysis in R

4 June

9.00 am – 12.00 noon

GP-S-506

Book

Hands-on training materials

Session 1 - Intro to HPC

Session 2 - Variant calling analysis

Session 3 - Variant analysis using Nanopore data

Session 4: Metagenomics (amplicon sequencing analysis)

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