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Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
Narrating uncertainty: Variants of uncertain significance (VUS) in clinical exome sequencingDOI 10.1057/s41292-016-0020-5
Variants of uncertain significance: At the crux of diagnostic odysseySemantic proximity
The scary world of variants of uncertain significance (VUS): A hitchhiker's guide to interpretation.Semantic proximity
Will variants of uncertain significance still exist in 2030?Semantic proximity
The Challenge of Genetic Variants of Uncertain Clinical Significance : A Narrative Review.Semantic proximity
Imprecision medicine: Systematic gaps in reporting variants of uncertain significance (VUS) and their reclassifications.Semantic proximity
“To Me, It Was Significant”: The Ethics of Returning Variants of Uncertain Significance from Clinical Exome SequencingSemantic proximity
Transcriptome analysis provides critical answers to the “variants of uncertain significance” conundrumSemantic proximity
Enhancing Variant of Uncertain Significance (VUS) Interpretation in Neurogenetics: Collaborative Experiences from a Tertiary Care CentreSemantic proximity
Lost in .*Vcf Translation. From Data Fragmentation to Precision Genomics: Technical, Ethical and Interpretive Challenges in the Post-Sequencing EraSemantic proximity
Sequence Variants of Uncertain Significance: What to Do When Genetic Test Results Are Not Definitive.Semantic proximity
The landscape of reported VUS in multi-gene panel and genomic testing: Time for a changeSemantic proximity
VUSVista: Enhancing the Curation of Variants of Uncertain SignificanceSemantic proximity
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