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66 changes: 66 additions & 0 deletions config/ZWU2022_VIBRIO_TIMECOURSE.config
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/*
* AREE :: run configuration for ZWU2022_VIBRIO_TIMECOURSE (PRJNA852380)
*
* Deposited by Zhejiang Wanli University, no publication found. 9-month-old
* intertidal oysters (Qingdao), digestive gland; untreated controls and
* oysters 1, 3, 6, 12 and 24 h after Vibrio exposure, three libraries per
* group. Vibrio species, dose and route are not in the deposit.
*
* Five prespecified comparisons, each time point vs the untreated controls.
* Default = the meta_analysis_primary one (24 h):
*
* nextflow run workflows/rnaseq -config config/ZWU2022_VIBRIO_TIMECOURSE.config \
* -profile local,workstation
*
* --comparison_id vibrio_12h_vs_control --treatment_level V12h
* --comparison_id vibrio_6h_vs_control --treatment_level V6h
* --comparison_id vibrio_3h_vs_control --treatment_level V3h
* --comparison_id vibrio_1h_vs_control --treatment_level V1h
*
* aree fetch-samplesheet --bioproject PRJNA852380 --study ZWU2022_VIBRIO_TIMECOURSE \
* --label-field sample_alias \
* --label-pattern '^(?P<group>control|V1h|V3h|V6h|V12h|V24h)_?(?P<replicate>[1-3])$' \
* --condition-attribute group --attribute replicate --attribute isolate --attribute tissue \
* --attribute age --attribute isolation_source --attribute collection_date
*/

includeConfig 'base.config'

params {
mode = 'raw_reanalysis'

rnaseq {
study_id = 'ZWU2022_VIBRIO_TIMECOURSE'
// Null so --comparison_id on the command line takes effect.
comparison_id = null
genome_assembly = 'GCF_963853765.1'
annotation_version = 'GCF_963853765.1-RS_2024_06'
processed_results = null
}

comparison_id = 'vibrio_24h_vs_control'

sample_sheet = 'data/studies/ZWU2022_VIBRIO_TIMECOURSE/samplesheet.tsv'

control_level = 'control'
treatment_level = 'V24h'

// FASTQ are not committed (59 GB for all 18 runs). Verify against ENA's MD5s
// from data/studies/ZWU2022_VIBRIO_TIMECOURSE/fastq_manifest.tsv.
reads = 'data/raw/ZWU2022_VIBRIO_TIMECOURSE/SRR*_{1,2}.fastq.gz'

transcript_fasta = 'data/reference/GCF_963853765.1/rna.fna'
gtf = 'data/reference/GCF_963853765.1/genomic.gtf'
tx2gene = 'data/reference/GCF_963853765.1/tx2gene.tsv'
salmon_index = null

outdir = 'results/rnaseq/ZWU2022_VIBRIO_TIMECOURSE'
}

process {
// 18 HiSeq X Ten 2x150 libraries, 20.6-27.6 M read pairs. Sized for a 16 GB machine.
withName: 'SALMON_INDEX' { cpus = 8; memory = '12 GB'; time = '4h' }
withName: 'SALMON_QUANT' { cpus = 8; memory = '12 GB'; time = '2h' }
withName: 'TRIM_FASTP' { cpus = 4; memory = '8 GB'; time = '2h' }
withName: 'FASTQC' { cpus = 2; memory = '4 GB'; time = '1h' }
}

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{
"workflow_name": "aree-rnaseq",
"workflow_version": "0.1.0-scaffold",
"mode": "raw_reanalysis",
"study_id": "ZWU2022_VIBRIO_TIMECOURSE",
"comparison_id": "vibrio_12h_vs_control",
"input_files": [
{
"name": "ZWU2022_VIBRIO_TIMECOURSE_vibrio_12h_vs_control_dge_standardized.tsv",
"sha256": "b859f699cec7ac7e68671c7fc2d822c2276b3561d62c26af901c9eea3dd3d96f"
}
],
"parameters": {
"mode": "raw_reanalysis",
"study_id": "ZWU2022_VIBRIO_TIMECOURSE",
"comparison_id": "vibrio_12h_vs_control",
"outdir": "results/rnaseq/ZWU2022_VIBRIO_TIMECOURSE",
"exclude_samples": [],
"control_levels": [
"control"
],
"treatment_levels": [
"V12h"
],
"replicate_unit": null,
"covariates": [],
"single_end": false,
"se_adapter": null,
"tag_seq": false,
"viral_reference": null
},
"deseq2_design": {
"design": "~condition",
"covariates_requested": [],
"covariates_used": [],
"covariates_dropped_constant": [],
"tag_seq": false,
"length_model": "tximport average transcript length offsets",
"n_libraries_or_units": 6,
"residual_df": 4
},
"software_versions": {
"DIFFERENTIAL_EXPRESSION_DESEQ2": {
"bioconductor-deseq2": "1.42.1",
"bioconductor-tximport": "1.30.0",
"r-base": "4.3.2"
},
"FASTQC": {
"fastqc": "0.12.1"
},
"SALMON_INDEX": {
"salmon": "2.3.4"
},
"SALMON_QUANT": {
"salmon": "2.3.4"
},
"SAMPLE_QC": {
"multiqc": "1.9"
},
"STANDARDIZE_OUTPUT": {
"pandas": "2.3.3",
"python": "3.9.6"
},
"TRIM_FASTP": {
"fastp": "1.3.6"
},
"EMIT_MANIFEST": {
"python": "3.9.6"
}
},
"software_versions_not_captured": {
"RENDER_REPORT": "renders this manifest, so it runs afterwards; its versions.yml is published to rnaseq/reports/"
},
"container_engine": null,
"reference": {
"genome_assembly": "GCF_963853765.1",
"annotation_version": "GCF_963853765.1-RS_2024_06",
"transcript_fasta": "data/reference/GCF_963853765.1/rna.fna",
"gtf": "data/reference/GCF_963853765.1/genomic.gtf",
"tx2gene": "data/reference/GCF_963853765.1/tx2gene.tsv",
"salmon_index": null,
"files": [
{
"name": "genomic.gtf",
"sha256": "ab5443f889932ef3e860d47e23801dd94a2b6a4a508f807e0349dfaccea79600"
},
{
"name": "rna.fna",
"sha256": "297d49baac2fd3187db957c3dcd150e58ed2a61c3867b61dbdd83ba9b683c386"
},
{
"name": "tx2gene.tsv",
"sha256": "170cae75beb05c1afd9b7b3dbed4bdeb4225c16f9aab757ccc00c2b449092d18"
}
],
"bundle": null
},
"workflow_start": "2026-10-16T20:13:54.448549-07:00",
"qc_metrics": {
"mean_reads_per_sample": null,
"mean_mapping_rate_percent": null,
"n_samples": null,
"note": "QC metrics are not populated in processed_results_harmonization mode or in this unexecuted scaffold run."
},
"viral_load": null,
"warnings": [
"reference_bundle_provenance_missing: no reference_provenance.json beside the reference files; fetch them with `aree fetch-reference` to record where they came from"
]
}
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