Demographic analysis of Brassica oleracea
Follows GATK4 best practices (https://software.broadinstitute.org/gatk/best-practices/workflow?id=11145)
Implemented as a Snakemake workflow (https://snakemake.readthedocs.io/en/stable/index.html)
- Clean up filtering steps
- Add adjustable parameters & metrics for filtering criteria (depth, missingness)
- More efficient use of scratch space
- Include sample ids & read groups in bwa-mem step (thanks, Michelle!): bwa mem -R
$(echo "@RG\tID:$ {LANE}_${SAMPLE}\tSM:$SAMPLE\tLB:${SAMPLE}.1\tPL:ILLUMINA") -a $B73FA $R1 $R2 - Add a config file to specify samples/reference/paths/etc. (will make workflow more general)
- include variable for scratch directory
- add rule for generating mappability mask using SNPable
- Find a better solution to create input for ADMIXTURE (right now requires manual edit of chr names and snp ids)
Snakefile provides general organization (names of samples, calls other scripts/rules)
/rules contains rules (*.smk) that tell snakemake what jobs to run; organized broadly into categories
-
mapping.smk - map reads to reference genome
- download fastq files (
fasterq-dump) - trim adapters (
Trimmomatic PE) - map to reference genome (
bwa mem; B. oleracea HDEM reference) - sort BAM files (
gatk/SortSam) - mark duplicates with Picard (
gatk/MarkDuplicates) - add read groups with Picard (
gatk/AddOrReplaceReadGroups)
- download fastq files (
-
calling.smk - call variants
- identify raw SNPs/indels (
gatk/HaplotypeCaller) - combine GVCFs (
gatk/GenomicsDBImport) - joing genotyping (
gatk/GenotypeGVCFs)
- identify raw SNPs/indels (
-
filtering.smk - filter SNPs
- select SNPs (
gatk/SelectVariants) - apply hard filters (
gatk/VariantFiltration) - export diagnostics (qual, quality depth, depth, marker quality, etc.) (
gatk/VariantsToTable) - remove sites with missing data and select biallelic SNPs (
gat/SelectVariants) - filter on individual sample depth (
gatk/VariantFiltration+gatk/SelectVariants) - export filtered depth for each accession (
gatk/VariantsToTable) - combine vcfs into a single file (
bcftools concat)
- select SNPs (
-
smc.smk - estimate population size history with
SMC++- convert vcf to smc format - requires mappability mask (
smc++ vcf2smc) - fit population size history with cross-validation (
smc++ cv) - fit population size history without cross-validation (
smc++ estimate)
- convert vcf to smc format - requires mappability mask (
-
admixture.smk - maximum likelihood estimation of individual ancestries
- create input file (some bash commands + LD pruning in
plink) - run admixture (
admixture)
- create input file (some bash commands + LD pruning in
To run the workflow:
- Create a conda environment (only need to do this once)
conda create -c conda-forge -c bioconda -n bodem snakemake
install the SLURM executor plugin
conda install -c bioconda snakemake-executor-plugin-slurm
install dadi python module
conda install -c conda-forge dadi
to access for future use, start a screen session with screen and use:
source activate bodem
-
If running on a cluster, update the cluster config file (submit.json)
-
Dry run to test that everything is in place...
snakemake -n -
Submit the workflow with
./submit.sh
├── LICENSE
├── Makefile <- Makefile with commands like `make data` or `make train`
├── README.md <- The top-level README for developers using this project.
├── data
│ ├── external <- Data from third party sources.
│ ├── interim <- Intermediate data that has been transformed.
│ ├── processed <- The final, canonical data sets for modeling.
│ └── raw <- The original, immutable data dump.
│
├── docs <- A default Sphinx project; see sphinx-doc.org for details
│
├── models <- Trained and serialized models, model predictions, or model summaries
│
├── notebooks <- Jupyter notebooks. Naming convention is a number (for ordering),
│ the creator's initials, and a short `-` delimited description, e.g.
│ `1.0-jqp-initial-data-exploration`.
│
├── references <- Data dictionaries, manuals, and all other explanatory materials.
│
├── reports <- Generated analysis as HTML, PDF, LaTeX, etc.
│ └── figures <- Generated graphics and figures to be used in reporting
│
├── requirements.txt <- The requirements file for reproducing the analysis environment, e.g.
│ generated with `pip freeze > requirements.txt`
│
├── src <- Source code for use in this project.
│ ├── data <- Scripts to download or generate data
│ ├── features <- Scripts to turn raw data into features for modeling
│ ├── models <- Scripts to train models and then use trained models to make
│ │ predictions
│ └── visualization <- Scripts to create exploratory and results oriented visualizations
Project based on the cookiecutter data science project template. #cookiecutterdatascience