Open pontikos opened 7 years ago
what data would this include? And would it be one file per patient or for all patients?
Easiest solution would be to create another endpoint for the CSV (maybe using csv.DictWriter
) and then I can add the UI button and the accomplying JS...
DECIPHER requires, but a few of these will be blank for us:
Internal reference number or ID HGVS code Genome assembly Transcript Gene name Intergenic Chromosomal sex Open-access consent Age at last clinical assessment Prenatal age in weeks Note Mother's phenotype Father's phenotype Inheritance Pathogenicity Phenotypes Genotype Responsible contact
pat1 chr7:g.103969467C>G GRCh37/hg19 NM_199000 LHFPL3 No 46XX Yes 5 Some free text note Shares similar phenotype (dominant inheritance plausible) Shares similar phenotype (dominant inheritance plausible) De novo constitutive Definitely pathogenic 1249, 252, 1518, 1892 Homozygous Please see instructions
I agree I'll write an endpoint to export the data.
This would be useful for export our data and importing it in to DECIPHER for example.