CLEAR:Composition of Likelihoods for Evolve And Resequence Experiments

##Overview CLEAR is a tool for identifying selection in time-series pooled-sequencing data. A bioRxiv preprint is available here.

##Requirements CLEAR is written in python which uses numba and pandas packages.You can install required packages by running

conda install pandas numba

##Running To obtain and run CLEAR simply execute

git clone https://github.com/bafnalab/CLEAR && cd CLEAR && python demo.py