kyook
commented
3 years ago I was thinking about this for the last couple of days. It actually might be easier for people to pick a phenotype first then be able to assign multiple genes and their alleles to the one phenotype, there should be an output line for each gene(allele) to match how things are captured in postgres.
valearna
[ ] include gene name with allele in variant column
[ ] need to figure out how to annotate NOT phenotypes. - this paper has NOT phenotypes 10.17912/micropub.biology.000367. perhaps we can add a column next after Phenotype terms called "Not observed" with a check box. The annotation would read for example. n728n398 dye filling abnormal NOT observed PHA/PHB
[x] when adding more than one term to the list, the highlighting makes the individual terms hard to read.
. perhaps add a more distinct border around the terms. This could be more about the longer terms, but most phenotype terms are going to be at least two words long
[x] I don't seem to be able to enter a phenotype statement, I'm using chrome if that matters