FAQ¶
Pipeline initialisation¶
Workflow defines configfile config_chip.yml but it is not present or accessible.¶
This error occurs when the pipeline is run without a config file present in the working directory. Ensure that seqnado-config has been run before starting the pipeline and that you are in the new directory created by seqnado-config.
Follow the Configuration Guide instructions to create a config file.
Singularity configuration¶
Workflow Error¶
Failed to pull singularity image from library://asmith151/seqnado/seqnado_pipeline:latest:
FATAL: Unable to get library client configuration:
remote has no library client (see https://apptainer.org/docs/user/latest/endpoint.html#no-default-remote)
Fix:
re-run seqnado init: See the Initialisation Guide
or
Optional configuration¶
Can I merge multiple samples into a single sample?¶
Yes, you can merge multiple samples into a single sample to generate merged bigWig files and consensus peaks. To do this, you need to create a design file that specifies the samples to be merged. The design file should have a column named "merge" that specifies the samples to be merged e.g.:
| sample | r1 | r2 | merge |
|---|---|---|---|
| sample-control-rep1 | /path/to/sample-control-rep1_R1.fastq.gz | /path/to/sample-control-rep1_R2.fastq.gz | control |
| sample-control-rep2 | /path/to/sample-control-rep2_R1.fastq.gz | /path/to/sample-control-rep2_R2.fastq.gz | control |
| sample-control-rep3 | /path/to/sample-control-rep3_R1.fastq.gz | /path/to/sample-control-rep3_R2.fastq.gz | control |
| sample-treated-rep1 | /path/to/sample-treated-rep1_R1.fastq.gz | /path/to/sample-treated-rep1_R2.fastq.gz | treated |
| sample-treated-rep2 | /path/to/sample-treated-rep2_R1.fastq.gz | /path/to/sample-treated-rep2_R2.fastq.gz | treated |
| sample-treated-rep3 | /path/to/sample-treated-rep3_R1.fastq.gz | /path/to/sample-treated-rep3_R2.fastq.gz | treated |