Support for heterozygous/homozygous genotype categories?

[jpcartailler]

Greetings,

I found BnpC is while testing out infSCITE and think it might help us with deciphering our SCS data. I have an initial question - according to the docs All matrix entries must be of the following: 0|1|3/" ", where 0 indicates the absence of a mutation, 1 the presence, and a 3 or empty element a missing value..

I'm interested in running our categorical genotype data, which is very similar to your input requirements:

Our input	BnpC input
0-reference	0 indicates the absence of a mutation
1-heterozygous mutation	1 the presence
2-homozygous mutation	1 the presence
3-unknown	3 or empty element a missing value

Is there any facility, or plans, on including hetero/homozygous genotype distinction in BnpC?

Thanks! JP