Open karlnyr opened 7 months ago
Plan is to analyse eternaltahr with its negative control ACC9713A25 which has reads and of low quality, requesting flow cell HVNHGDSX2 to fetch the data back to hasta so that we can add it to ACC9713A25 temporarily.
ACC9713A25
Analysis completed without any issues. This means that we can now begin the process of adding data for all negative controls to hk as well! @Clinical-Genomics/sysdev, could you prioritize this? The current situation is very prone to mistakes, and the metagenomic samples are quite time-sensitive.
It is not pipeline relevant. This is on an organisation level where we would like to store all reads for samples that are negative controls @diitaz93
@karlnyr What issue would this resolve? Is it a requirement for taxprofiler being implemented in production?
This would resolve two things:
Edited issue, as this would be changed for all negative controls, not specifically for metagenomic ones.
Changes reverted.
Blocked until the changes can be implemented in LIMS.
Description
Negative controls require all reads linked to their housekeeper bundle and have the read counts added to the sample in statusdb and LIMS.
Suggested solution
When we parse the demultiplexing stats we do get the number of reads from the sample, the next step would be to (a) check if a sample is a negative control or (b) find the metagenomic negative control on a flow cell, and handle it differently.This can be closed when
Negative controls have their reads added to the sample bundle, statusdb, and LIMS disregarding read quality.
Clarification
Negative controls by definition won't pass our QC after sequencing and won't have the fastq files linked to them. Negative controls should always have their data transferred. These can be used by the customer to filter out any noise from the prep. Also, in the new metagenomic analyses they are needed.
The above four steps are required to pass.
Second Clarification