A sequence analysis tool to detect emergent, rare mutations in sub-sets of cell populations
For full documentation please refer to DeepSNVMiner_documentation.pdf
If you use DeepSNVMiner please cite:
Andrews TD, Jeelall Y, Talaulikar D, Goodnow CC, Field MA. 2016. DeepSNVMiner: a sequence analysis tool to detect emergent, rare mutations in subsets of cell populations. PeerJ 4:e2074 https://doi.org/10.7717/peerj.2074