-
Hello, zhengxia:
The Dapars is really useful and very nice for me to analysis APA in last days.
But recently I gained some strand-specific RNA-Seq data wich build like dUTP ways, does dapars sup…
-
### Objective: As a user with a pipette, I would like the DCP to process 10x v2 and v3 single-nuclei sequencing data (snRNA-seq) so that I can submit such data to the DCP and view the results in the d…
-
hello there,
I have encountered the Error : TypeError: __init__() got an unexpected keyword argument 'log_level' , while trying to analyse some NanoPore seq data.
i have implemented the steps presen…
-
I am presently engaged in studying the genome of Dalbergia, commonly known as Indian rosewood. Regrettably, I currently lack RNA-Seq data or protein files pertinent to this genome. Nonetheless, I ha…
-
Hi,
I got the following error message from kallisto quant, but kallisto seems to be on version 0.50.0 and it doesn't explain what those versions refer to.
```
[quant] fragment length distributio…
-
https://carpentries-incubator.github.io/bioc-intro/index.html
May be worth linking to or otherwise mentioning? Or at some point coordinating with.
-
I've been using STARsolo for single-cell RNA-seq analysis, and I have a question about how it handles SMART-seq data. I understand that SMART-seq does not employ UMIs or cell barcodes, which are typic…
-
Hi Authors,
I have tried to post-process the example-output with "run_blast_os_par.py" but failed. Any advice? I see that the original paper is now online on Nature Comms so I hope there will be m…
-
I am new to RNA seq analysis. I installed Linux in VirtualBox because I have Windows,and I read that Star does not run on windows. Howe, I can not get it to run on Linux from VirtualBox either. Can yo…
-
Hi,
I want to use ABIS for deconvolution of the RNA-Seq profiles generated from the whole blood ( only RBCs are removed by RBC lysis buffer) remaining all cells are their. I have run premilinary ana…