nextflow run nf-core/smrnaseq \
-profile <docker/singularity/.../institute> \
--input samplesheet.csv \
--genome 'GRCh37' \
--mirtrace_species 'hsa' \
--protocol 'illumina' \
--outdir <OUTDIR>
sample,fastq_1
Clone1_N1,s3://ngi-igenomes/test-data/smrnaseq/C9-N1-R1_S7_L001_R1_001.fastq.gz
Clone1_N2,s3://ngi-igenomes/test-data/smrnaseq/C9-N2-R1_S8_L001_R1_001.fastq.gz
Control_N1,s3://ngi-igenomes/test-data/smrnaseq/Ctl-N1-R1_S1_L001_R1_001.fastq.gz
Control_N2,s3://ngi-igenomes/test-data/smrnaseq/Ctl-N2-R1_S2_L001_R1_001.fastq.gz
{
"max_cpus": 4,
"max_memory": "12.GB",
"max_time": "6.h",
"input": "https://github.com/nf-core/test-datasets/raw/smrnaseq/samplesheet/v2.0/samplesheet.csv",
"fasta":"https://github.com/nf-core/test-datasets/raw/smrnaseq/reference/genome.fa",
"mature": "https://github.com/nf-core/test-datasets/raw/smrnaseq/reference/mature.fa",
"hairpin": "https://github.com/nf-core/test-datasets/raw/smrnaseq/reference/hairpin.fa",
"mirna_gtf": "https://github.com/nf-core/test-datasets/raw/smrnaseq/reference/hsa.gff3",
"mirtrace_species": "hsa",
"protocol": "illumina",
"skip_mirdeep": true
}
nextflow run smrnaseq/ -profile docker --input samplesheet.csv -params-file myParams.json --outdir results
Tutorial here.
Follow the instructions in the
Tower
documentation to launch the pipeline.
export TOWER_ACCESS_TOKEN=<token>
export TOWER_WORKSPACE_ID=<id>
Can store in $HOME/.nextflow/config
tower {
enabled = true
accessToken = '<token>'
workspaceId = '<id>'
}
Notes found here.