Closed nwhand closed 1 year ago
Dear @nwhand, you can use any of the fast5 file produced by run the run as all the fast5 files contain metadata about the run!
@jourdren, thank you, how do i isolate or extract a fast5 file from a folder of fast5 files? (the minion groups together 4000 fast5 files in one folder).
You just had to set the path of just one Fast5 file in the command line. As an example, see the --fast5-source
the argument in the following command line:
$ toulligqc --report-name FAF0256 \
--barcoding \
--fast5-source /path/to/the/run/no_sample/20220728_1551_MC-110337_FAT79338_15385417/fast5/ FAT79338_9a380b24_0.fast5 \
--sequencing-summary-source /path/to/basecaller/output/sequencing_summary.txt \
--sequencing-summary-source /path/to/basecaller/output/barcoding_summary_pass.txt \ # (optional)
--sequencing-summary-source /path/to/basecaller/output/barcoding_summary_fail.txt \ # (optional)
--sequencing-summary-1dsqr-source /path/to/basecaller/output/sequencing_1dsqr_summary.txt \ # (optional)
--sequencing-summary-1dsqr-source /path/to/basecaller/output/barcoding_summary_pass.txt \ # (optional)
--sequencing-summary-1dsqr-source /path/to/basecaller/output/barcoding_summary_fail.txt \ # (optional)
--html-report-path /path/to/output/report.html \
--data-report-path /path/to/output/report.data \ # (optional)
--barcodes BC01,BC02,BC03
Hi, A colleague has shown me reports generated with toulligQC that would be great for me. However I am just a wet lab person! The output from the Nanopore Mk1c does not include a 'sequencing_telemetry' file. I see from the Github page that a fast5 file would be a fine substitute. Assuming this is true and the fastest way for me to get a report is to add a fast5 file, how do i isolate a fast5 file from the package of 4000 that is generated by the minion? (i think the default size of fast5 folders is 4000 reads).
Thanks, Nick H.