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**Is your feature request related to a problem? Please describe.**
When trying to analyze nanopore sequencing data with CRISPResso2, the runs fails due to insufficient memory. I believe this is arisi…
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Hi i am running mity via docker but encountered with some bam error, could not able to rectify it, actually i was trying to find out INDELS for long read ONT generated data, using minimap2 aligned bam…
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Hello!
I would love your opinion or advice with our method, and I have a few questions about how UMItools extract with a regex works.
I have nanopore long reads with dual 18bp UMIs, one on eac…
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Hi i am running mity via docker but encountered with some bam error, could not able to rectify it, actually i was trying to find out INDELS for long read ONT generated data, using minimap2 aligned bam…
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Hi,
I am trying to run mtdna server by installing it offline, however i am using nextflow first time. i am able to install the process but encountered with the error:
ERROR ~ Unable to parse con…
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Hi,
can I use purge_dups for nanopore based assemblies as well?
Thanks,
Jacqueline
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Hi,
Does Melon accept FastQ files from long-read metabarcoded data?
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Hallo i am using wgbstools to visualize my Nanopore Data. So everything worked but i have a few questions regarding the Output. I segmented the Bam file and vis it with wgstools
wgbstools vis -r 1…
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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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Dear developer
i am trying to build a hybrid assembly with Illumina pair reads and nanopore data from sequence biofilms, so i expected a highly complex environment compare to human gut microbiota. …