Open davmlaw opened 3 years ago
Might be nice to do per kit as well? So we know it has ever been seen in a kit?
Also per-patient, though it would be difficult to do this in a way that doesn't get super slow as you add more samples over time
Feature request for:
a node that filters on germline variants only or somatic variants only (each sample would have to be tagged beforehand as germline/somatic), and a node that filters on present in tumour + absent in germline (each tumour/germline pair would have to be tagged beforehand)
At the moment we have "Global variant zygosity count" which is non-germline samples
We can support multiple ones, we just only have 1 at the moment
Need to work out what people would like to split by, could be eg
Things that use the counts, ie "All variants node" and the analysis columns (db het count) need to choose what they join to