Enhancing Variant Prioritization in VarFish through On-Premise Computational Facial Analysis

被引:0
|
作者
Bhasin, Meghna Ahuja [1 ]
Knaus, Alexej [1 ]
Incardona, Pietro [1 ,2 ]
Schmid, Alexander [1 ]
Holtgrewe, Manuel [3 ]
Elbracht, Miriam [4 ]
Krawitz, Peter M. [1 ]
Hsieh, Tzung-Chien [1 ]
机构
[1] Rhein Friedrich Wilhelms Univ Bonn, Univ Hosp Bonn, Inst Genom Stat & Bioinformat, D-53127 Bonn, Germany
[2] Univ Bonn, Med Fac, Core Unit Bioinformat Data Anal, D-53127 Bonn, Germany
[3] Berlin Inst Hlth, CUBI Core Unit Bioinformat, D-10117 Berlin, Germany
[4] Rhein Westfal TH Aachen, Inst Human Genet & Genom Med, Med Fac, D-52062 Aachen, Germany
关键词
variant prioritization; facial imaging analysis; next-generation phenotyping; rare diseases; exome sequencing analysis; CANDIDATE GENES; DIAGNOSTICS; GENETICS; GENOMICS;
D O I
10.3390/genes15030370
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Genomic variant prioritization is crucial for identifying disease-associated genetic variations. Integrating facial and clinical feature analyses into this process enhances performance. This study demonstrates the integration of facial analysis (GestaltMatcher) and Human Phenotype Ontology analysis (CADA) within VarFish, an open-source variant analysis framework. Challenges related to non-open-source components were addressed by providing an open-source version of GestaltMatcher, facilitating on-premise facial analysis to address data privacy concerns. Performance evaluation on 163 patients recruited from a German multi-center study of rare diseases showed PEDIA's superior accuracy in variant prioritization compared to individual scores. This study highlights the importance of further benchmarking and future integration of advanced facial analysis approaches aligned with ACMG guidelines to enhance variant classification.
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页数:11
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