A tool to detect CLIP-seq peaks.
Please visit our wiki page to learn more about usage of clipper: https://github.com/YeoLab/clipper/wiki/CLIPper-Home
# recreate PYTHON3 conda environment
cd clipper
conda env create -f environment3.yml
conda activate clipper3
pip install .
guix install clipper
eclip
repository here.# shows all the options
clipper -h
# minimal command
clipper -b YOUR_BAM_FILE.bam -o YOUR_OUT_FILE.bed -s hg19
cd clipper/clipper/test
python -m unittest discover
Right now the test coverage is still not 100%. And some subprocess warnings are not handled.
How do use additional reference genome? See here for instructions: Supporting additional species
Where can I use specify the Input bam file? Currently CLIPper does include input normalization. The input normalization pipeline is in another repository: Merge Peaks
please open an issue in the repo. or email Charlene hsher@ucsd.edu
Yeo GW, Coufal NG, Liang TY, Peng GE, Fu XD, Gage FH. An RNA code for the FOX2 splicing regulator revealed by mapping RNA-protein interactions in stem cells. Nat Struct Mol Biol. 2009;16(2):130-137. doi:10.1038/nsmb.1545
Lovci MT, Ghanem D, Marr H, et al. Rbfox proteins regulate alternative mRNA splicing through evolutionarily conserved RNA bridges. Nat Struct Mol Biol. 2013;20(12):1434-1442. doi:10.1038/nsmb.2699