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## Question
Hi Seqan-Team,
I just recently read about XOR Filters and that they were superior to Bloom Filters in regards to memory usage and query time. Do you plan (or maybe already started) t…
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I have noticed that the chloroplast and mitochondrion do not assemble with hifiasm. I am not expecting to get the full plastid assembled correctly, but I don't see anything. When I align the corrected…
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Hello,
I have an error `Segmentation fault` when I run arriba v2.4.0. I tried to debug with gdb.
Below, you can find all the logs.
```
(gdb) run -x /data/sample.bam -o /data/sample_arriba_st…
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Hi there!
I'm following the guidelines for the mixed oriented reads case, trying to demultiplex a bunch of 4 different files (x_R1.fastq.gz, x_R2.fastq.gz, y_R1.fastq.gz and y_R2.fastq.gz).
Afte…
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Hi there,
I installed precompiled ngmlr 0.2.7, copied the demo command for Nanopore run, and replaced with my own ref.fa and whole genome seq.fastq.gz files. It immediately gave "segmentation fault…
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Hi, I'm trying to do de novo assembly of a fungi genome that has an average size of 53Mbp.
I keep getting this error
```
[Wed Jan 29 14:52:12 CET 2020] Processing pe library reads
[Wed Jan 29 15:…
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## User story
>As a curator
>I want the post uploadscript to work as expected
>So that I can use it
## Acceptance criteria
>Given I have uploaded a dataset using the upload script
>Whe…
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Hi, all
I got the error message while using the command
pggb -i in.fa.gz -o output -n 3 -t 24 -p 90 -s 500 -M -V 'An-1:#'
The Error log message is as follows
[smoothxg::(1-3)::main] loadin…
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Hello,
I have HiFi data for a diploid insect, with an estimated genome size of ~425 Mb according to flow cytometry data. I used Kraken to filter reads and make sure there were no adapters in the re…