Add guide on SNV filtering based on cell type information

The putative SNV call sets could be further filtered based on mutation distribution across the cell types derived from scRNA-seq data

accelerated mutation scanning at the single cell level

v1.5.0

Add files via upload

Add segment-based sequencing scan at single cell level

v1.1.0

include segment scan on somatic module

Monopogen-1.0.0

This is the first release including both germline and somatic SNV calling modules