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Minor README changes
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Luquette committed May 10, 2019
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Expand Up @@ -115,9 +115,12 @@ scansnv \
See `scansnv -h` for more details on arguments.

After SCAN-SNV completes, single sample results are available in the
Rdata file
Rdata file `demo/scansnv/[single_cell_sample_name]/somatic_genotypes.rda`.
SNVs that pass SCAN-SNV's calling thresholds will have `pass=TRUE` in the
`somatic` data frame (see below).

**NOTE**: a VCF output option is forthcoming.
```
demo/scansnv/[single_cell_sample_name]/somatic_genotypes.rda
# Called sSNVs can be extracted from the data frame via
R> load('demo/scansnv/[single_cell_sample_name]/somatic_genotypes.rda')
R> somatic[somatic$pass,]
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