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Hello,
I have a doubt with the use of remora. I want to make a resquiggling, similar to what can be done with Tombo, to use it in other programs. However, I don't see a function similar to this, ev…
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Hi,
I tried to run f5c eventalign using the merged blow5 file that I created from slow5tools and here is the error I got:
```
[slow5_idx_init::INFO] Index file not found. Creating an index at '…
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Hello!
Could you please provide me with the information on your plan about adapter trimming incorporating to the Dorado. It is the feature I rely on in my workflow and it was that I used in guppy. No…
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Hi, developer.
Thank you for providing a useful tool!
I have run xpore and generated the result with HEK293T-WT-rep2 and HEK293T-Mettl3-KO-rep2 successfully.
I wanted to check whether I correctly…
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貼吧活動：(請查閱 [SARS-CoV-2 Timeline by 2020.02.21](https://github.com/agorahub/_meta/blob/agoran/theagora/sari/Memorandum_2020-02-21_SARS-CoV-2-Timeline_Nathan.pdf?raw=true), by Nathan :cloud: )
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Dear Canu team,
I have ultra-long read sequencing data (PromethiON flow cell from Oxford Nanopore) of _Drosophila erecta_ (genome size 145MB). Basecalling was done using Guppy version 6.5.7.
Prio…
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Hi!
I've come to realize that I ran canu with genomeSize set at double what I'm now expecting from my species (set 2.3Gb, reality ~1Gb). How much, if at all, would this affect the output? Metrics l…
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We have generated some sequencing data from short (50 bp) oligonucleotides with strand-specific modifications and I was wondering if there is a way to use Remora to identify signatures of these modifi…
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I completed the canu tutorial for the ONT data with no problems. I then tried to use my own data by running the following command:
`/home/hh/canu/Linux-amd64/bin/canu \
-p HBV -d HBV-oxford \
…