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Hi there,
I noticed that IsoQuant provide a parallelisation option within the DatasetProcessor class (more specifically in collect_reads method) but it is not entirely clear to me if the parallelisation is done at the read/read group level or at the chromosome level.
I was wondering if you can please clarify which parallelisation strategy was used? I tried to increase the number of threads in my IsoQuant run (using aligned BAM files as input and with a single chromosome only in the BAM, FASTA and GTF files), but when running htop, it looks like only one thread is running while the others stays suspended.
Thanks and kind regards,
Andrian
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