Dear Ajay and Dan,
You have proposed that your first limitation is that you are only limited to coding variants, and you do not quantify the contribution of rare non-coding variants. So if I can use BHR to estimate the heritability in non-cosing regions. Moreover, can I use BHR to estimate heritability for structural variants, such as SV and CNV?
Sorry for all the questions. I am keen to get this working, but am a relative novice at this!
Best wishes,
Bob
Dear Ajay and Dan,
You have proposed that your first limitation is that you are only limited to coding variants, and you do not quantify the contribution of rare non-coding variants. So if I can use BHR to estimate the heritability in non-cosing regions. Moreover, can I use BHR to estimate heritability for structural variants, such as SV and CNV?
Sorry for all the questions. I am keen to get this working, but am a relative novice at this!
Best wishes,
Bob