# ------------------------------------------------ # CITATION.cff file created with {cffr} R package # See also: https://docs.ropensci.org/cffr/ # ------------------------------------------------ cff-version: 1.2.0 message: 'To cite package "ClinicalVariantR" in publications use:' type: software license: MIT title: 'ClinicalVariantR: ACMG/AMP Germline Variant Interpretation from Annotated VCF Files' version: 0.99.0 abstract: ClinicalVariantR is an interactive Shiny platform for evidence-based germline variant classification under ACMG/AMP 2015 guidelines. It accepts VEP-, SnpEff-, or ANNOVAR-annotated VCF files, applies automated and curator-guided ACMG criteria, supports streaming analysis of large call sets, and exports structured per-criterion evidence with reproducibility metadata. authors: - family-names: Rafique given-names: Safa email: safa.sandhu@gmail.com orcid: https://orcid.org/0000-0003-2646-8106 - family-names: Mahmood given-names: Naeem email: naeem.sbb@pu.edu.pk - family-names: Sabar given-names: Muhammad Farooq email: farooq.sbb@pu.edu.pk preferred-citation: type: manual title: 'ClinicalVariantR: ACMG/AMP Germline Variant Interpretation from Annotated VCF Files' authors: - family-names: Rafique given-names: Safa orcid: https://orcid.org/0000-0003-2646-8106 email: safa.sandhu@gmail.com - family-names: Mahmood given-names: Naeem email: naeem.sbb@pu.edu.pk - family-names: Sabar given-names: Muhammad Farooq email: farooq.sbb@pu.edu.pk year: '2026' notes: R package version 0.99.0 url: https://github.com/safarafique/ClinicalVariantR repository: https://biocstaging.r-universe.dev repository-code: https://github.com/safarafique/ClinicalVariantR commit: 2c08894bfba4c5dd5aa1f1e066898d62a9918a13 url: https://github.com/safarafique/ClinicalVariantR date-released: '2026-07-08' contact: - family-names: Rafique given-names: Safa email: safa.sandhu@gmail.com orcid: https://orcid.org/0000-0003-2646-8106