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Allow no reads to start #19
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I have handling for this in the ONT on-prem snakemake. Basically when the yaml is created, empty fastq_pass dirs are never included in the DAG. The script prints out all the failed barcodes and includes them in the "analyses beginning" email notification. This is, I assume, not the intended behavior for a GUI like MIRA since we still want to show said samples in our figures/etc? |
Correct. We still want the sampleID to show up in the IRMA summary table, but will have 0 reads to start…
From: Kristine Lacek ***@***.***>
Sent: Wednesday, June 21, 2023 11:03 AM
To: CDCgov/MIRA ***@***.***>
Cc: Rambo Martin, Benjamin (CDC/DDID/NCIRD/ID) ***@***.***>; Author ***@***.***>
Subject: Re: [CDCgov/MIRA] Allow no reads to start (Issue #19)
I have handling for this in the ONT on-prem snakemake. Basically when the yaml is created, empty fastq_pass dirs are never included in the DAG. The script prints out all the failed barcodes and includes them in the "analyses beginning" email notification. This is, I assume, not the intended behavior for a GUI like MIRA since we still want to show said samples in our figures/etc?
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This MR pulls my empty barcode dir branch into illumina-flu branch (big boy) |
reformat.sh
crashes snakemake if run on an empty fastq. Empty fastq can be generated fromcat
step when fastq_pass/barcodeXX directory exists and there are no fastqs within it. I assume the directory was created by Minknow but that all of barcodeXX reads were put in fastq_fail. Not sure...The text was updated successfully, but these errors were encountered: