I noticed that after running the same workflow (v1.7.1) on the same data that output files differ. For example 'wc -l' results:
111935 de_analysis/filtered_transcript_counts_with_genes.tsv #Run 1
111922 de_analysis/filtered_transcript_counts_with_genes.tsv #Run 2
I am not sure when the analyses start diverging (probably during Stringtie). However, output BAM files are the same.
Is there a way of being able to rerun the workflow and get exactly the same output? The intention is to be able to delete large fastq and fasta files, and recreate in the future if needed.
I noticed that after running the same workflow (v1.7.1) on the same data that output files differ. For example 'wc -l' results:
111935 de_analysis/filtered_transcript_counts_with_genes.tsv #Run 1
111922 de_analysis/filtered_transcript_counts_with_genes.tsv #Run 2
I am not sure when the analyses start diverging (probably during Stringtie). However, output BAM files are the same.
Is there a way of being able to rerun the workflow and get exactly the same output? The intention is to be able to delete large fastq and fasta files, and recreate in the future if needed.