Reproducibility
Learning outcomes
After having completed this chapter you will be able to:
- Understand the importance of reproducibility
- Apply some basic rules to support reproducibilty in computational research
Material
Some good practices for reproducibility
During the exercise you will be guided to adhere to the following basic principles for reproducibility:
- Execute the commands from a script in order to be able to trace back your steps
- Number scripts based on their order of execution (e.g.
01_download_reads.sh
) - Give your scripts a descriptive and active name, e.g.
06_build_bowtie_index.sh
- Make your scripts specific, i.e. do not combine many different commands in the same script
- Refer to directories and variables at the beginning of the script
Keep re-evaluating your code structure
If you start a project it can be difficult to know what kind of analyses you are going to run, and how they interrelate. While working on a project, therefore re-evaluate readability of your project structure, and do not hesitate to change script numbering, names or contents.
By adhering to these simple principles it will be relatively straightforward to re-do your analysis steps only based on the scripts, and will get you started to adhere to the Ten Simple Rules for Reproducible Computational Research.
Exercises
Throughout the exercises today and tomorrow we will work on three different ‘subprojects’:
- Preparing references by indexing
- Alignment and variant calling on one sample (‘mother’)
- Alignment, variant calling and filtering on all samples
We store the scripts required for these subprojects in different subdirectories of ~/workdir/scripts
named:
A-prepare_references
B-mother_only
C-all_samples
You can already create these directories now with:
cd ~/workdir/scripts/
mkdir -p \
A-prepare_references \
B-mother_only \
C-all_samples
By the end of day 2 ~/workdir/scripts
should look (something) like this:
scripts
├── A_prepare_references
│ ├── A01_download_course_data.sh
│ ├── A02_create_bwa_index.sh
│ ├── A03_create_vcf_indices.sh
│ └── A04_create_fasta_index.sh
├── B_mother_only
│ ├── B01_alignment.sh
│ ├── B02_get_alignment_statistics.sh
│ ├── B03_sort_alignment.sh
│ ├── B04_compress_alignment.sh
│ ├── B05_add_readgroups.sh
│ ├── B06_mark_duplicates.sh
│ ├── B07_get_alignment_stats_after_md.sh
│ ├── B08_index_alignment.sh
│ ├── B09_perform_bqsr.sh
│ ├── B10_run_haplotypecaller.sh
│ └── B11_variants_to_table.sh
└── C_all_samples
├── C01_alignment_sorting_compression.sh
├── C02_add_readgroups.sh
├── C03_mark_duplicates.sh
├── C04_index_alignment.sh
├── C05_perform_bqsr.sh
├── C06_run_haplotypecaller.sh
├── C07_create_genomicsdb.sh
├── C08_genotype_gvcfs.sh
├── C09_select_SNPs.sh
├── C10_select_INDELs.sh
├── C11_filter_SNPs.sh
├── C12_filter_INDELs.sh
├── C13_merge_filtered.sh
├── C14_extract_mother_only.sh
├── C15_evaluate_concordance.sh
├── C16_extract_mother_before_filtering.sh
└── C17_evaluate_concordance_before_filtering.sh