{"id":"W2011094690","doi":"10.1086/424388","title":"Integrated Evaluation of DNA Sequence Variants of Unknown Clinical Significance: Application to BRCA1 and BRCA2","year":2004,"lang":"en","type":"article","venue":"The American Journal of Human Genetics","topic":"BRCA gene mutations in cancer","field":"Biochemistry, Genetics and Molecular Biology","cited_by":385,"is_retracted":false,"has_abstract":false,"ca_institutions":"","funders":"National Cancer Institute; Medical Research and Materiel Command; Canadian Institutes of Health Research; National Institutes of Health; Breast Cancer Research Foundation","keywords":"Genetics; Clinical significance; Biology; Sequence (biology); Disease; Family history; Computational biology; DNA sequencing; Gene; Bioinformatics; Medicine; Internal medicine","routes":{"ca_aff":false,"ca_fund":true,"ca_venue":false,"about_ca":false,"invisible_to_affiliation_only":true},"retraction":null,"screen":null,"machine_scores":{"provisional":true,"baseline":true,"maturity_gate_passed":false,"score_opus":0.047699188417183,"score_gpt":0.383924855429786,"score_spread":0.336225667012603,"validation_status":"score_only:v0-immature-baseline","note":"Baseline scores from an immature model (maturity gate not passed). Scores rank; they never assert a category."}}