Comments (5)
Hi Jessie,
Thank you for using RASflow.
Snakemake will always check the final "output" (the input of rule end
) and if it finds that the required file is already there, it will do nothing but just say "Nothing to be done."
And the final "output" of QC is: config["FINALOUTPUT"] + "/" + config["PROJECT"]+ "/fastqc/report_quality_control.html"
(this can be found in workflow/quality_control.rules), and the first two paras are defined in the config file configs/config_main.yaml
. So I suggest to check whether that file is already there (even an empty file with that name) and delete it if it exists. And rerun the workflow.
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Thank you for the detail explanation Xiaokang! This issue is solved, but now I have another question: can we start the pipeline directly from DEA without alignment?
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Yes, but it's tricky. Because you need to make sure that the quantification of transcript/gene is already done and the files are organized in a way that RASflow can recognize (refer to the output from quantify_trans.rules
if transcriptome is used as ref, or align_count_genome.rules
if genome is used as ref. Then you can use the Snakemake file for DEA:
nice -5 snakemake -s workflow/dea_trans.rules 2>&1 | tee logs/log_dea_trans.txt
if you're using transcriptome as reference, or
nice -5 snakemake -s workflow/dea_genome.rules 2>&1 | tee logs/log_dea_genome.txt
if the genome is used as reference.
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Problem solved! Thanks a lot Xiaokang!
from rasflow.
Glad to hear that. I'll then close this issue. Feel free to open a new issue when you have another problem.
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