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"output_reads": r"INFO Number of reads out: (\d+)",
"positions_deduplicated": r"INFO Total number of positions deduplicated: (\d+)",
"mean_umi_per_pos": r"INFO Mean number of unique UMIs per position: ([\d\.]+)",
"max_umi_per_pos": r"INFO Max. number of unique UMIs per position: (\d+)",
"version": r"# UMI-tools version: ([\d\.]+)",
}
do not match the UMI-Tools log file output when using --extract_method regex (exact command via nf-core/rnaseqhere). The corresponding log file looks the following (full file attached):
2024-01-25 00:20:39,419 INFO Parsed 10000000 reads
2024-01-25 00:20:40,180 INFO Input Reads: 10077011
2024-01-25 00:20:40,180 INFO regex does not match read1: 9215286
2024-01-25 00:20:40,180 INFO regex matches read1: 861725
2024-01-25 00:20:40,180 INFO regex does not match read2: 752463
2024-01-25 00:20:40,180 INFO regex matches read2: 109262
2024-01-25 00:20:40,180 INFO Reads output: 109262
MultiQC version: 1.14 (but regexes are the same in latest)
UMI-Tools version: 1.1.4 (latest)
For the vis, I'd probably suggest a stacked bar graph with colors: (1) mismatched read1, (2) matched read1 but mismatched read 2, (3) matched both reads; total of these is the input read number
Description of bug
The regexes provided in the UMI-Tools module
MultiQC/multiqc/modules/umitools/umitools.py
Lines 105 to 114 in d26af5e
do not match the UMI-Tools log file output when using
--extract_method regex
(exact command via nf-core/rnaseq here). The corresponding log file looks the following (full file attached):MultiQC version:
1.14
(but regexes are the same in latest)UMI-Tools version:
1.1.4
(latest)File that triggers the error
RMGI_wt_250_48h-3.umi_extract.log
MultiQC Error log
No error, but UMI-Tools panel is absent.
Before submitting
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