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- Used BASH to carry out basic and introductory tasks
- Worked with simple biological datasets
- Softwares used:
- fastqc (quality control)
- multiQC (assembling quality control reports)
- fastp (trimming sequence adapters)
- fastx (fastq_to_fasta : convert fastq to fasta)
- bwa (assembling genomes)
- samtools (manipulating sam/bam/cram files)
Note: All the results are stored in output file and the sample datasets are in the raw_reads file
- Followed the tutorial from:
- https://github.com/Fredrick-Kakembo/Somatic-and-Germline-variant-Identification-from-Tumor-and-normal-Sample-Pairs/blob/main/README.md
- https://training.galaxyproject.org/training-material/topics/variant-analysis/tutorials/somatic-variants/tutorial.html
- Prepared a summary report of the task