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# Issue Report
## Please describe the issue:
Unable to run dorado basecaller with supv5.0.0 models. sup@v4.3.0 works fine.
## Steps to reproduce the issue:
*Please list any steps to repro…
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# Issue Report
Hello,
I was trying to get statistics of the % of pass and fail reads in a flow cell after parallelized basecalling by single pod5 on an HPC. I've seen that the number of reads ma…
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Hi, I used your tool to check the performance of porechop. After I ran porechop, I checked the adapter content in my result file with sequali. But I don't understand the "adapter content" item in the …
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[[Note: Please edit the title above and provide a description of the grid here.
Also check the ISO_3166-2 (https://en.wikipedia.org/wiki/ISO_3166-2)
codes if your grid uses countries or states/prov…
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# Issue Report
## Please describe the issue:
When using dorado to obtain methylated basecall info, the standard "a" and "c" methylation types but so does "21839".
What is this methylation ca…
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> Methylframe
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Now that modification calls are being rolled into Dorado's direct RNA basecalling models, we need ways to evaluate those calls, and set sane cutoffs for probabilities/likelihood scores where we trust …
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Hi I am trying to figure out all the models for all my fastq.gz files, but I am getting this error message when I run one sample:
```
(base) [kvigil@qbc141 medaka]$ medaka tools resolve_model --au…
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Hi,
I wondered if I could change the parameter `--trim` in Dorardo when running `wf-basecalling`. Based on the description in Dorado's documentation (https://github.com/nanoporetech/dorado?tab=read…
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I am interested in using Nano 3PSeq (https://www.nature.com/articles/s41592-022-01714-w) to sequence polyA'd and non-polyA'd transcripts. Previously this protocol used tailfindr for tail length callin…