Introduction to NGS Data
- Date: Tue, 1 Jan - Tue, 31 Dec 2019
- Location: TBC
- Contact: Bioinformatics Hub +61 8313 1207
- Email: firstname.lastname@example.org
This is a full day workshop introducing you to the basic layout of important files used in high-throughput sequencing applications, such as FASTQ, BAM, BED, VCF and GFF files.
- Postgraduate students can receive credit for 6 CaRST hours upon completion of the course.
- Undergraduate Students and other researchers are also welcome.
This is a full day workshop introducing you to the basic layout of important files used in high-throughput sequencing applications, such as fastq, bam, bed, vcf and gff files. In addition we will cover the key areas such as:
- Assessing the Quality of your data
- Aligning Reads to a Genome
- Inspecting Files using Bash
- Visualising Data
- Identifying Variants
Prerequisites and co-requisite courses
Attendance at Introduction to Bash, or alternatively prior experience with Bash or an HPC environment.
No dates for 2019 have been scheduled.
Please contact the Bioinformatics Hub to express your interest in attending the next event.