AUTHOR=Qian Xinye , Wang Jun , Wang Meng , Igelman Austin D. , Jones Kaylie D. , Li Yumei , Wang Keqing , Goetz Kerry E. , Birch David G. , Yang Paul , Pennesi Mark E. , Chen Rui TITLE=Identification of Deep-Intronic Splice Mutations in a Large Cohort of Patients With Inherited Retinal Diseases JOURNAL=Frontiers in Genetics VOLUME=12 YEAR=2021 URL=https://www.frontiersin.org/journals/genetics/articles/10.3389/fgene.2021.647400 DOI=10.3389/fgene.2021.647400 ISSN=1664-8021 ABSTRACT=
High throughput sequencing technologies have revolutionized the identification of mutations responsible for a diverse set of Mendelian disorders, including inherited retinal disorders (IRDs). However, the causal mutations remain elusive for a significant proportion of patients. This may be partially due to pathogenic mutations located in non-coding regions, which are largely missed by capture sequencing targeting the coding regions. The advent of whole-genome sequencing (WGS) allows us to systematically detect non-coding variations. However, the interpretation of these variations remains a significant bottleneck. In this study, we investigated the contribution of deep-intronic splice variants to IRDs. WGS was performed for a cohort of 571 IRD patients who lack a confident molecular diagnosis, and potential deep intronic variants that affect proper splicing were identified using SpliceAI. A total of six deleterious deep intronic variants were identified in eight patients. An