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This repository was archived by the owner on Jul 25, 2024. It is now read-only.
Hi,
I tried to run poreplex on a minION run using the follwing command to basecall and demultiplex barcodes from direct RNA sequencing: poreplex -i 20191122_1000_MN24929_FAL01495_e9928ec8/fast5/ -o poreplex_demultiplex --barcoding --fast5 --basecall --parallel 20
This results in an error:
== Analysis settings ======================================
* Input: fast5/20191122_1000_MN24929_FAL01495_e9928ec8/fast5/
* Output: poreplex_demultiplex
* Processes: 20
* Presets: rna-r941.cfg
* Basecall on-the-fly: Yes (albacore 2.3.4)
* Trim 3' adapter: No
* Filter concatenated read: No
* Separate by barcode: Yes
* Real-time alignment: No
* FASTQ in output: Yes
* FAST5 in output: Yes
* Basecall table in output: No
===========================================================
==> Processing FAST5 files
ERROR: [signal_analyzer.py:48] Unhandled exception ValueError: Unknown entries in loss dictionary: ['config', 'class_name']. Only expected following keys: ['dense_2']Task exception was never retrieved
future: <Task finished coro=<ProcessingSession.run_process_batch() done, defined at /home/graf/.local/lib/python3.6/site-packages/poreplex/pipeline.py:193> exception=CancelledError()>
concurrent.futures._base.CancelledError
Is there anything I need to do to get around that error?
First I tried the Fast5 files basecalled with Guppy with the same result. So I thought running the internal albacore basecalling will help, but unfortunately no luck!
Could you give me a hint what to do to solve that issue?