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I ran the pipeline (v3.3) on 6 paired end samples. It seems that the pipeline is not preserving the R2 sample name properly after trimming. See the fastq status check heatmaps before and after trimming. For example, JCV1_1 remains as JCV1_1 but JCV1_2 becomes JCV1. Same happens for all the samples.
Before:
After:
Also, this affects the General stats table where the FastQC trimmed values (the last three columns) are in the wrong row.
This issue also occurred on a different RNAseq project where I used v3.0 of the pipeline.
Here are the pre and post trimming FastQC results. looks like the 'sample' column in the Post FastQC is not named correctly for the R2 read
drpatelh
changed the title
R2 sample names are not preserved in the FastQC trimmed Status Check heatmap nor General Stats table
Error with post-trimmed read 2 sample names from FastQC in MultiQC
Sep 22, 2021
I ran the pipeline (v3.3) on 6 paired end samples. It seems that the pipeline is not preserving the R2 sample name properly after trimming. See the fastq status check heatmaps before and after trimming. For example, JCV1_1 remains as JCV1_1 but JCV1_2 becomes JCV1. Same happens for all the samples.
Before:

After:

Also, this affects the General stats table where the FastQC trimmed values (the last three columns) are in the wrong row.
This issue also occurred on a different RNAseq project where I used v3.0 of the pipeline.
Here are the pre and post trimming FastQC results. looks like the 'sample' column in the Post FastQC is not named correctly for the R2 read
Pre trimming:
Post trimming:
@drpatelh thinks the issue is due to this line
rnaseq/assets/multiqc_config.yaml
Line 62 in 8094c42
For reference, this issue was discussed on the rnaseq Slack channel on Monday Aug 16th 2021
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