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Dear @all
I think this question would be more appropriate here, so I referenced it here (https://github.com/nanoporetech/dorado/issues/1089)
Thank you for your time.
Kind regards
Zheng zhuqi…
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This shows up, when I am selecting RNAseq or other NGS (genomics). If I do genomics, it might be that I act…
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An R-CMD check error occurs when running this example code for `reverseOperonSeq()`:
```
❯ checking examples ... [14s/15s] ERROR
Running examples in ‘MolEvolvR-Ex.R’ failed
The error most like…
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We want to include genomics data in this workshop.
Pasting from #2 (@jorgepda )
I found this dataset from this [paper](http://science.sciencemag.org/content/347/6226/1138) and been running a co…
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Hi,
Is it possibe to use CRIS tool for WES data?
All the best!
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Hi @scottcain ,
There are some contextual data changes coming from our partners at Public Health Ontario (PHO) that'd require some changes in the virusseq data portal and its metadata schema.
B…
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Hi,
I tried integrating three PBMC snRNAseq data from 10X Genomics multiome datasets with two scRNA seq data from a 10X Genomics Public dataset. However, all the data from the multiome clusters sep…
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I actually found out about Squash through the page at http://jdlm.info/articles/2017/05/01/compression-pareto-docker-gnuplot.html and realized that the genomics dataset that is used for those tests wo…
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In order to import data to SKG backend, genomic data should be provided as CSV files
aim11 updated
1 month ago
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I want to use bamcoverage to produce some publication quality graphs with R. I got a bit puzzled how coverage is actually calculated, because it seems to be higher than what I see in IGV and also what…