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/*
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
Nextflow config file for running minimal tests
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
Defines input files and everything required to run a fast and simple pipeline test.
Use as follows:
nextflow run nf-core/ampliseq -profile test,<docker/singularity> --outdir <OUTDIR>
----------------------------------------------------------------------------------------
*/
process {
resourceLimits = [
cpus: 4,
memory: '15.GB',
time: '1.h'
]
}
params {
config_profile_name = 'Test profile'
config_profile_description = 'Minimal test dataset to check pipeline function'
// Input data
primer_fwd = "GTGYCAGCMGCCGCGGTAA"
primer_rev = "GGACTACNVGGGTWTCTAAT"
input = params.pipelines_testdata_base_path + "ampliseq/samplesheets/Samplesheet_v3.tsv"
metadata = params.pipelines_testdata_base_path + "ampliseq/samplesheets/Metadata.tsv"
dada_ref_taxonomy = "gtdb=R07-RS207"
cut_dada_ref_taxonomy = true
qiime_ref_taxonomy = "greengenes85"
// ASV generation
sample_inference = "independent"
// ASV postprocessing
vsearch_cluster = true
decontam = "decontaminate"
filter_ssu = "bac"
max_len_asv = 255
//this is to remove low abundance ASVs to reduce runtime of downstream processes
min_samples = 2
min_frequency = 10
//produce average barplots
metadata_category_barplot = "treatment1"
//restrict ANCOM analysis to higher taxonomic levels
tax_agglom_max = 2
sbdiexport = true
qiime_adonis_formula = "treatment1,mix8"
diversity_rarefaction_depth = 500
// Test ANCOMBC
ancombc = true
ancombc_formula = "treatment1"
ancombc_formula_reflvl = "treatment1::b"
ancombc_effect_size = 2
ancombc_significance = 0.00001
// Test ANCOMBC2
ancombc2 = true
ancombc2_formula = "treatment1"
ancombc2_formula_reflvl = "treatment1::b"
}