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**Steps to Reproduce**
1. Switch to Macro mode -> Sequence mode
2. Add sequence letters and select any
3. Right-click on selected letters and choose 'Modify in RNA builder'
4. Press 'Esc' button
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### Please make sure these conditions are met
- [X] I have checked that this issue has not already been reported.
- [X] I have confirmed this bug exists on the latest version of scanpy.
- [x] (option…
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Hi Alex, I'm very new to github so please forgive me if I'm maybe not following the exact protocol for issues and questions.
I've been using STAR for aligning single cell RNA data for several years n…
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Hi, is it possible for RNA reads simulation to include parameters defining distribution of poly(A) lengths? (For simplicity it can be just mean+sd). Thanks!
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#### Which new datasets are being added with this release?
#### What is the sample breakdown (number of WGS, WXS, RNA-Seq, Panel, Methylation, other)?
https://d3b.atlassian.net/browse/BIXU-3767
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Hi,
I am trying the tool for the quantification of nuclear RNA, after my recent tweets with Lior Patcher.
Every commands in the Velocity tutorial seems to work, but I want only the quantificatio…
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I am getting the above error even though the region is present in my data. What could be wrong?
```bash
./LDBlockShow-1.40/bin/LDBlockShow -InVCF haplotype_gene_quantification/g3_variants/haptags_…
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Hi! I reached out to one of my colleagues who does some great work in the small RNA world (also specifically for Cancer) and he suggested this book/tutorial he wrote: [https://pubmed.ncbi.nlm.nih.gov/…
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How to download the RNA stralign datasets and the Achive II datasets from your paper
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Hello!
Is it possible to use SATC with RNA-seq data?