Whole-exome sequencing in undiagnosed genetic diseases: interpreting 119 trios.
Whole-exome sequencing in undiagnosed genetic diseases: interpreting 119 trios.
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DOI：
10.1038/gim.2014.191
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发表时间：
2015-10
期刊：
影响因子：
--
通讯作者：
Goldstein DB
中科院分区：
文献类型：
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作者：
Zhu X;Petrovski S;Xie P;Ruzzo EK;Lu YF;McSweeney KM;Ben-Zeev B;Nissenkorn A;Anikster Y;Oz-Levi D;Dhindsa RS;Hitomi Y;Schoch K;Spillmann RC;Heimer G;Marek-Yagel D;Tzadok M;Han Y;Worley G;Goldstein J;Jiang YH;Lancet D;Pras E;Shashi V;McHale D;Need AC;Goldstein DB
Despite the recognized clinical value of exome-based diagnostics, methods for comprehensive genomic interpretation remain immature. Diagnoses are based on known or presumed pathogenic variants in genes already associated with a similar phenotype. Here, we extend this paradigm by evaluating novel bioinformatics approaches to aid identification of new gene–disease associations. Genet Med 17 10, 774–781. We analyzed 119 trios to identify both diagnostic genotypes in known genes and candidate genotypes in novel genes. We considered qualifying genotypes based on their population frequency and in silico predicted effects we also characterized the patterns of genotypes enriched among this collection of patients. Genet Med 17 10, 774–781. We obtained a genetic diagnosis for 29 (24%) of our patients. We showed that patients carried an excess of damaging de novo mutations in intolerant genes, particularly those shown to be essential in mice (P = 3.4 × 10−8). This enrichment is only partially explained by mutations found in known disease-causing genes. Genet Med 17 10, 774–781. This work indicates that the application of appropriate bioinformatics analyses to clinical sequence data can also help implicate novel disease genes and suggest expanded phenotypes for known disease genes. These analyses further suggest that some cases resolved by whole-exome sequencing will have direct therapeutic implications. Genet Med 17 10, 774–781.
