Abstract：
:Next generation sequencing is transforming clinical medicine and genome research, providing a powerful route to establishing molecular diagnoses for genetic conditions; however, challenges remain given the volume and complexity of genetic variation. A number of methods integrate patient phenotype and genotypic data to prioritise variants as potentially causal. Some methods have a clinical focus while others are more research-oriented. With clinical applications in mind we compare results from alternative methods using 21 exomes for which the disease causal variant has been previously established through traditional clinical evaluation. In this case series we find that the PhenIX program is the most effective, ranking the true causal variant at between 1 and 10 in 85% of these cases. This is a significantly higher proportion than the combined results from five alternative methods tested (p = 0.003). The next best method is Exomiser (hiPHIVE), in which the causal variant is ranked 1-10 in 25% of cases. The widely different targets of these methods (more clinical focus, considering known Mendelian genes, in PhenIX, versus gene discovery in Exomiser) is perhaps not fully appreciated but may impact strongly on their utility for molecular diagnosis using clinical exome data.
journal_name
Sci Repjournal_title
Scientific reportsauthors
Pengelly RJ,Alom T,Zhang Z,Hunt D,Ennis S,Collins Adoi
10.1038/s41598-017-13841-ysubject
Has Abstractpub_date
2017-10-18 00:00:00pages
13509issue
1issn
2045-2322pii
10.1038/s41598-017-13841-yjournal_volume
7pub_type
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