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Hi sorry to bother you I'm trying to use methylartist for my data, but I am encountering some problems.
First I have my chromosomes named as contig_1, contig_2 ect... in all my data is it a problem…
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Hi,
I am wondering if there is currenly a way to do barcode demultiplexing and duplex calling using only dorado, and if so, what would be the best way to do it?
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Hello, where could i find my system_id on my OceanStor Dorado 3000 V6 ?
Thanks for answering.
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Hello,
I process 6 different samples that I mapped against the same reference genome (the mitochondria) using Dorado. Using Samtool coverage, I checked that all my sample covered 100% of my genome …
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Hello,
Our lab currently trying the cDNA-PCR barcoding kit (PCB111.24) for our _de novo_ assembly transcriptome project. Our issue is that after using pychopper, we still somehow have the barcode se…
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# Issue Report
## Please describe the issue:
*Please provide a clear and concise description of the issue you are seeing and the result you expect.*
## Steps to reproduce the issue:
I used…
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dear author:
I submit the job to run on a single node of the cluster, but after a long time, there is no output. The single-node CPU is aarch64 architecture, the cpu model is kunpeng920, the GPU is A…
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Thank you for the excellent program. I am currently testing the latest version with several parameters for ONT ultra-long read datasets. However, I noticed a potential omission in usage options and ex…
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In the `fastq.gz` that Dorado outputs, I see that a semicolon is sometimes included as part of the read ID. A semicolon is used to separate attribute-value pairs in the `VCF` format. Could you please …
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I don't know if the author is aware of the issue with incomplete removal of sequence adaptors and barcodes.
Specifically, when using tools such as Dorado Demux, Porechop, and Guppy_barcoder to trim a…