Closed Byronxy closed 4 years ago
Hi, thanks for the testing. BRIE2 takes a list of sam files in the -S
option instead of each sam file.
Please follow the quick start example: https://brie.readthedocs.io/en/latest/quick_start.html or the the new demo file: https://github.com/huangyh09/brie/blob/master/examples/brie2_demo.sh
Also, please upgrade to v2.0.2 from github
pip install -U git+https://github.com/huangyh09/brie
Let us know if it resolves your issue.
Yuanhua
Hi, I successfully run the brie_count. However, I got an error when running brie-quant
Good. It looks you only have three cells, and all genes are filtered out, as by default --minCell=30
, namely only genes having >= 30 cells with unique reads are kept. You could set --minCell=0
.
Thanks a lot! I got the result!
Hi, I set up the environment as you described. And I tested with the example data and got the error.