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First step is to figure out which services are offered for each provider. We should look at each product as well, in case the analysis services also differ by product.
- [ ] Nebula Genomics
- [x] …
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Dear Nicolas,
Just a follow up question for the issue #216
How do I know the right % of mtDNA reads of the total sequence reads that mapped to the whole mtDNA? I'm doing a comparison between the…
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Hello,
I have been using Exomiser for some time but have a specific issue that is causing some confusion:
I have a list of a handful of variants (1-3) that I want to input into Exomiser and esse…
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Dears,
Thanks for making a great program. I've run into an error message and I am looking for guidance on how to resolve it.
I have installed MitoFlex on my Linux Ubuntu OS and have installed al…
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Hi,
I actually succeeded before in setting up the environment, but recently I changed my virtual machine because the former one will be offline for a week.
Here some errors were reported:
[ini…
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Hi, I am working with very small bacterial genomes, and when trying to annotate the smallest of them using the latest Prokka I came upon a curious error.
Contigs above a certain length (120kb is OK)…
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Reads which have a relatively short sequence that does not map to a reference sequence and a relatively long sequence which maps perfectly to one end of a reference sequence aren't mapped. Is there an…
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The error occurs because environment.yaml is missing. How can I solve this?
The same thing happened with docker.
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Hi there! I have been getting the error while completion of final assembly on two separate data-sets. The error is as following "Checking coverage of final assembly. Final assembly is the last afin it…
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Funannotate implements a strict word limit for FASTA headers. This doesn't correspond with some of the current NCBI requirements. For example, when indicating that a contig is a mitochondrion, they r…