Note: genome.fa and genome-var.fa differ at positions 100, 600 and 1100.
You'll need khmer branch feature/collect-variants.
To run:
bash make.sh # produces reads.fa, reads2.fa, and mix.fa
bash do.sh # produces {reads,reads2,mix}.sorted.bam
bash readscorr.sh # correct reads.fa against self
bash varcorr.sh # correct mix.fa against self, retaining variants (!!)
bash vardown.sh # downsample mix.fa against self, adaptively oversampling variant containing regions (!!)