sofia
sofia
Hello, I am having troubles to interpretate the output from rankNet(cellchat, mode = "comparison", stacked = T, do.stat = TRUE)$data. I am attaching a pdf file to explain my workflow....
Hello, thanks for developing this package. I am trying to compare my clusters with the clusters of a previously published scRNA seq dataset. The reference clusters don't have the same...
Dear fgbio team, I would like to use AnnotateBamWithUmis, however I am not very sure about the steps to take. I couldn't find any tutorial that refers to AnnotateBamWithUmis. I...
Hello! Thanks for the great software. I am running fastp for paired end reads obtained from an Illumina machine, and feeding it with a list of adaptors. It worked good...
Hi, may I ask if it is normal (correct) to detect different adaptors sequence in the paired reads? (attached a picture with the example) Thanks for your help! [fastp.pdf](https://github.com/OpenGene/fastp/files/11868397/fastp.pdf)
Hi, Thanks for your great package. I have paired end RNA seq data, with three fastq files per samples. I used Hisat2 to align R1 and R2 reads, and then...
Hello, I'm currently working with spikeinterface using Maxwell data. While I haven't encountered any issues reading MaxOnw data, I'm facing a problem with MaxTwo data. My objective is to read...
Hi, I really want to try this package, but unfortunately I haven't been able to install it. I tried on a centos machine and an ubuntu machine, but in both...
## 1. Bug description I was previously using the following code to extract the GWAS summaries of **1)** Biological insights from 108 schizophrenia-associated genetic loci. Nature, 2014 **2)** Genome-wide association...
Hi, I have been using the function scur.get_potential_auto_merge() to get pairs f neurons to be merged and then I merge them with .merge(pairs). It works well most of the time,...