-
## Checklist before submitting the issue:
- [Kind of] The issue is strongly related to the MiXCR software
- [X] The issue can be reproduced with [the most recent version](https://github.com/mila…
-
Hi,
I am new learner of PASA and Trinity. I can not understand why 4 steps.
I found in the pipline "Build a Comprehensive Transcriptome Database Using Genome-guided and De novo RNA-Seq Assembly…
-
https://mp.weixin.qq.com/s/6DnwrIwxdX7q7c7ktkrVrg
ixxmu updated
2 years ago
-
Hi,
when I use " formatter_class" to subparsers$add_parser, it seems not work,but for ArgumentParser, it is OK 。
```
### the script
sub_st_deconv
-
Hi all,
I've seen a few whispers on the ABySS Google Groups pages indicating that it's possible to use Abyss for de novo assembly of whole exome (not genome) data. One thing Shaun has replied to a …
-
https://mp.weixin.qq.com/s/FhQfFkn29PwQtQlCYWsVSg
ixxmu updated
2 years ago
-
Hi, I analyzed a sample with trust, and used trust-barcoderep-to-10X.pl to convert barcode_report to 10X format (10X_report). According to the converted data, I counted the clonetypes of productive, b…
-
Hello, thank you for your fantastic toolkit . We would like to implement *Connectome* , but in your paper the usage seems to be restricted to Single Cell omics experiments. In our case, we have perfo…
-
I did the _scaden process_ step using a bulk RNA-seq dataset (named NewData) that has about 18,000 genes, and then ran _predict_ using an older dataset that shares only about 15,000 genes with NewData…
-
https://mp.weixin.qq.com/s/dEYKrM3oW3ILt7Zaumva_A
ixxmu updated
2 years ago