[svtoolkit-help] Genome STRiP software qustion

[王四华 <ws...@12...>]

Dear experts：
I have some doubt about Genome STRiP software.
As we all know:
To run discovery or genotyping on a single sequenced genome or a small set of genomes, you need to call your data against a background population, 
such as a set of genomes from the 1000 Genomes Project.  The background population does not need to be matched to the target individuals.
But how could I use the background population?  If I hava a single sequenced genome sample (named: Sample AA),and how can I use the background population? 
If I have 20 background sample.I did not find the parameter for the background population. I only know the parameter (- I) for the input bam file for target sample AA. 
Expect your reply! Thank you very much!