Before starting the Core, complete all of the following:
Checklist |
---|
Access Volac's genomics server |
Secure connection set up |
Raw data saved in a sub-folder inside input_core |
Sample sheet made and saved inside input_core |
Starting the Core
First enter this command:
cd ~/genome_tools/Core
Then enter one of the following commands, depending on the file extension of your raw read data.
If the file extension of your raw read data is .fastq.gz
, enter this command, replacing YYYY-MM-DD
with a date:
nextflow run core.nf --indexpath 'index_YYYY-MM-DD.csv' --inputfq 'YYYY-MM-DD/*_R{1,2}_001.fastq.gz'
If the file extension of your raw read data is .fq.gz
, enter this command, replacing YYYY-MM-DD
with a date:
nextflow run core.nf --indexpath 'index_YYYY-MM-DD.csv' --inputfq 'YYYY-MM-DD/*_R{1,2}_001.fq.gz'
The sample sheet
Use --indexpath 'index_YYYY-MM-DD.csv'
to tell the Core which sample sheet to use.
For example,
--indexpath 'index_2022-04-29.csv'
The raw data
Use --inputfq 'YYYY-MM-DD/*_R{1,2}_001.fastq.gz'
to tell the Core which raw data to use.
For example,
--inputfq '2022-04-29/*_R{1,2}_001.fastq.gz'
Example
The full entry will be:
nextflow run core.nf --indexpath 'index_2022-04-29.csv' --inputfq '2022-04-29/*_R{1,2}_001.fastq.gz'
Exception (for MiSeq raw data)
If your samples were sequenced using MiSeq technology (rather than NextSeq) an additional 5 characters are required to start the Core, _L001
.
Use --inputfq 'YYYY-MM-DD/*_L001_R{1,2}_001.fastq.gz'
to tell the Core which raw data to use.
Everything else remains the same.
MiSeq example
The full entry will be:
nextflow run core.nf --indexpath 'index_2022-04-29.csv' --inputfq '2022-04-29/*_L001_R{1,2}_001.fastq.gz'