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https://mp.weixin.qq.com/s/tV7SfHHf855vq8QW7ncSPg
ixxmu updated
2 years ago
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I downlowd xl and peak file from https://imaps.goodwright.com/collections/868/ and run: peka -i tardbp-egfp-hd-hek293-1-20201021-ju_mapped_to_genome_single.bed1 -x tardbp-egfp-hd-hek293-1-20201021-ju_…
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Hello! Thank you for this repository!
I apologize, I am very new to this and saying I am confused is an understatement. I am trying to determine regions of Non-B-DNA in the _Drosophila melanogaster…
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Hi, I´m fairly new with ONT data, and I want to run megadolon to call modified bases on Paspalum notatum (a grass). When I run it with default parameters it works just fine, but I was wondering if I c…
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Although this potential recombinant sublineage doesn't meet the minimum criteria of 50 sequences, I thought it's still worth proposing, considering:
- It first emerged back in January, and is stil…
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Hi,
After updating to 2.8.1 the drawing speed of Xquartz is extremely slow, basically almost impossible to work in a remote X11 Nedit window for example. It turned out to be the Xquartz version.
…
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The error showed up when runing pyscenic on step one using jupyter through python 3.8.2 version.
the detail posted below,
#Version
scanpy==1.4.4.post1 anndata==0.6.22.post1 umap==0.4.3 numpy==1.1…
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Hello,
At UMCCR, we use arriba as a fusion caller for WTS clinical samples for cancer patients. Arriba is part of our WTS production pipeline setup and works great.
We have recently encountered …
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Hello,
I'm planning on running nanodisco on isolate genomes that I have generated native and WGA data for recently. My lab has a fast Guppy GPU Docker image for demultiplexing and basecalling the r…
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Having issues figuring out the error message from flair correct. The command and error message are:
```
$python flair.py correct -f gencode.v30lift37.fixed.annotation.gtf -c hg19.chrom.sizes.fixed2…