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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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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 \
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### Data Owner Name
DNAstack terms of use,Creative Commons Attribution 4.0 International,CC BY-4.0
### Data Owner Country/Region
United States
### Data Owner Industry
Life Science / Healthcare
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*************edited November 20***************
**TRACKER**
BA.2.86: -C6541T,A7842, C8293T, G8393A (new query thx to @aviczhl2 )
JN.1 QUERY: C18894T, T15756A, A7842, -C6541T
XDD Query : C6541T…
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Hello,
I'm running MOP2 on a Macintosh computer with Nextflow 21.10.6 build 5660 and Guppy 6.0.1. MOP2 will run if I start it with the fastq files, but if I try to run basecalling with fast5 files …