-
### Aims/objectives.
We currently have BID-seq, eTAM-seq, and GLORI, amounting to a total of 65 dataset. We need to add more data from the public domain, esp. if we aim for a publication. We cannot…
-
Dear nicheNetR Team,
Following my nichnetr analysis, I have generated a list of target genes and I am interested in assigning pathways to these genes. Could you kindly advise if there is a function…
-
cc: @lpantano @gurgese @ThomasDesvignes @mhalushka @mlhack @keilbeck @BastianFromm @ivlachos @TJU-CMC @sinanugur @Bastami @haebhardt
Let's discuss `Variant` attribute that will give the informatio…
-
Hi,
May I ask how does souporcell handle situations with extremely uneven (smth like 95% of cells from individual 1 and 5% - from individual 2, or even more skewed) ratios of cells from different i…
-
I have been trying to assemble a 10Mb genome with uncorrected nanopore data (3-4 chromosomes expected). We have a lot of data, is that the reason Flye fails at the end?
[2019-06-22 11:00:05] INFO: …
-
---
Author Name: **Bert Klauninger** (Bert Klauninger)
Original Redmine Issue: 2476, https://redmine.open-bio.org/issues/2476
Original Date: 2008-03-26
Original Assignee: Bioperl Guts
---
For some …
-
Here is the updated list they provided Dec 15 2023.
We are generally interested to find gene pairs where:
- there is a strong Cell Painting ORF pos or neg correlation (column E: ORF_similarity_ab…
-
# Migrating create react app to nextjs
```
yarn add next
```
and so it begins
Add .next/ to `.gitignore`.
Initially I thought I would have to change the directory structure, but ne…
-
This issue is a place to discuss how to create and collaborate on flexible scRNA-Seq workflows.
I've tried to collate the main points of the discussion that started [here](https://github.com/galax…
-
Hello!
I have run fastp twice, once outputting to a folder fastp/ and then using those fastq files as input to another fastp run which then outputs to a parallel folder fastp_trim36/. Running multi…