-
![1280851631](https://user-images.githubusercontent.com/10949202/108296873-4d131100-71d5-11eb-8162-7da17a4c3c8d.jpg)
在表面加一层水,跑到6ps的时候出现这种情况,这是不是水分子解离了?
-
Hi,
I am processing an scRNA-seq dataset containing 14 samples. For each sample, I performed the standard QC filtering based on nFeatures and mitochondrial gene percentage, followed by the identifi…
-
Hi drneavin,
contacting you here since it's the only way I found ;)
I read the Demuxafy preprint with much interest (very nice work), and had a question. One area of the field which I feel still nee…
plger updated
2 years ago
-
As pointed out by @nafisa-valieva , the difference between the records LIT1932Mashaf and LIT5654MGessew (used for instance in ESmy022) does not become clear from the records. A difference is encoded i…
-
See
1. https://eartharxiv.org/repository/view/7665/
2. https://www.resfrac.com/blog/digesting-the-bonkers-incredible-off-the-charts-spectacular-results-from-the-fervo-and-forge-enhanced-geothermal-p…
-
Scanning with my Jenkins i get following page title.
"/var/lib/jenkins/workspace/crawler_ci_report"
I would like it to be configurable.
-
HI,
I am interested in applying C-SIDE to a dataset where I did the celltype deconvolution without a reference scRNA-seq dataset due to a lack of a good reference. From my reading of the method thi…
-
Based upon previous exploration of the data, I suspect that some cells with high cell cycle related gene expression are being called as doublets (likely because I have 2 or 3 different clusters that a…
-
Hi,
Great tool, thank you for making it available to the community.
I have run souporcell on a number of scRNA-seq samples. Everything appears to go fine and the program runs to completion provi…
-
@xiaoyeye great tool! when I run analysis get error like this.
The adata file is a subset of a big file and then merge with the velocyto file.
```
(TFvelo_env) dengzhen@dengzhen-Super-Server:~/co…