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Dear @alekseyzimin,
which is the optimal fragment mean size and short-read size of the Illumina paired end reads in order to get the best results in a hybrid assembly using nanopore long-reads? Accor…
ghost updated
4 years ago
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Can I use this software on an already assembled partial mitogenome. The genome was sequenced as metagenomic environmental sample using Oxford Nanopore long read technology. Any help is appreciated
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This issue will track some issues with porting the 64-bit kernel to pcrel addressing. Once we have something reasonably working and found no good way to solve these, they should be raised with relevan…
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### Goal
Provide an optional Just-in-time compilation that dynamically translates the instructions into x86-64 instructions.
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Hi Sébastien,
I am not getting any results for -gene-ontology and I have followed the instructions from your 2012 paper git repo. It seems that the cds sequence part of the script was not working due…
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Hello.
Skesa is awesome assembler. But, I have stumbled on an issue and I was hoping you may be able to help. I detail what I have done so far and where I think the problem is below. Please let me …
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It would be helpful to have a bit in here describing specifying ordering for atomic instructions. I've looked around, and while I've determined that you can set the rl bit by adding a .rl on an atomic…
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# Critical Assesment of Metagenome Interpretation (CAMI)
CAMI is an open challenge for meta-omic's programs where the developers of said programs test out their programs on multiple different dataset…
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Hello, I am trying to align metagenomic sequences, when I run initPipeline with the following command I get the expected output:
`initPipeline -q -1 Unmapped.out.mate1 -d projectDir -i 300:800`
Pr…