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# Issue Report
I have previously basecalled data with the Rapid Sequencing kit (SQK-RAD114), and I sequenced now some samples with the Rapid Barcoding kit (SQK-RBK114.24)
I ran
## Run environme…
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Hello,
I have a question regarding the use of DeepSignal2 on the new version of nanopore sequencing. Since the sequencing data is no longer in the fast5 format, but in the pod5 format, I would like …
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**Context:**
I'm very new to DNA sequencing and bioinformatics, and I'm currently following the DADA2 tutorial for primer identification and removal. My sequence data was generated using Illumina Mi…
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Hi all,
EagleC had offered structural variants with great precision.
We did a high-depth sequencing of several well-known cell lines to test our hi-c experiments modified from classic in-situ …
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Hi, Developer.
Thank you for developing a useful tool.
I wanted to identify m6a sites from nanopore sequencing data. Before analyzing my data, I tried going through the steps in the document https…
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Hi,
Great tool and documentation! I've read on your documentation page that the tool might work with whole exome data - could you please provide more information on that? Is possible and is it rec…
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The genome size of the species I'm assembling is 2.6Gb, and the ONT data comes from dorado sup v5.0.0 (R10).
When I used 167GB data (>Q7, >10Kb) with "Nanopore-UL-May2022.conf", I got an assembly o…
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Hi,
I have successfully used DISCOVER with data from whole-exome sequencing. I am wondering whether I can use it with data from targeted sequencing data generated by MSK IMPACT or DFCI OncoPanel. A…
jud-b updated
5 months ago
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Hello!
I have ONT data of a single amplicon that is ~4500 bp in length and would like to identity SVs. I am interested in any SVs present, but specifically, there may be repeats introduced by a h…
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Dear developers,
Many thanks for such a great tool!
I have 32 fastq files sequenced from direct cDNA sequencing by nanopore, and compressed them into a fastq.gz file.
When running the rattle cluste…