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      Leveraging clinical intuition to improve accuracy of phenotype-driven prioritization

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          Abstract

          Purpose:

          Clinical intuition is commonly incorporated into the differential diagnosis as an assessment of the likelihood of candidate diagnoses based either on the patient population being seen in a specific clinic or on the signs and symptoms of the initial presentation. Algorithms to support diagnostic sequencing in individuals with a suspected rare genetic disease do not yet incorporate intuition and instead assume that each Mendelian disease has an equal pretest probability.

          Methods:

          The LIkelihood Ratio Interpretation of Clinical AbnormaLities (LIRICAL) algorithm calculates the likelihood ratio of clinical manifestations represented by Human Phenotype Ontology terms to rank candidate diagnoses. The initial version of LIRICAL assumed an equal pretest probability for each disease in its calculation of the posttest probability (where the test is diagnostic exome or genome sequencing). We introduce Clinical Intuition for Likelihood Ratios (ClintLR), an extension of the LIRICAL algorithm that boosts the pretest probability of groups of related diseases deemed to be more likely.

          Results:

          The average rank of the correct diagnosis in simulations using ClintLR showed a statistically significant improvement over a range of adjustment factors.

          Conclusion:

          ClintLR successfully encodes clinical intuition to improve ranking of rare diseases in diagnostic sequencing. ClintLR is freely available at https://github.com/TheJacksonLaboratory/ClintLR.

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          Most cited references32

          • Record: found
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          OMIM.org: leveraging knowledge across phenotype–gene relationships

          Abstract For over 50 years Mendelian Inheritance in Man has chronicled the collective knowledge of the field of medical genetics. It initially cataloged the known X-linked, autosomal recessive and autosomal dominant inherited disorders, but grew to be the primary repository of curated information on both genes and genetic phenotypes and the relationships between them. Each phenotype and gene is given a separate entry assigned a stable, unique identifier. The entries contain structured summaries of new and important information based on expert review of the biomedical literature. OMIM.org provides interactive access to the knowledge repository, including genomic coordinate searches of the gene map, views of genetic heterogeneity of phenotypes in Phenotypic Series, and side-by-side comparisons of clinical synopses. OMIM.org also supports computational queries via a robust API. All entries have extensive targeted links to other genomic resources and additional references. Updates to OMIM can be found on the update list or followed through the MIMmatch service. Updated user guides and tutorials are available on the website. As of September 2018, OMIM had over 24,600 entries, and the OMIM Morbid Map Scorecard had 6,259 molecularized phenotypes connected to 3,961 genes.
            • Record: found
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            Extensive sequencing of seven human genomes to characterize benchmark reference materials

            The Genome in a Bottle Consortium, hosted by the National Institute of Standards and Technology (NIST) is creating reference materials and data for human genome sequencing, as well as methods for genome comparison and benchmarking. Here, we describe a large, diverse set of sequencing data for seven human genomes; five are current or candidate NIST Reference Materials. The pilot genome, NA12878, has been released as NIST RM 8398. We also describe data from two Personal Genome Project trios, one of Ashkenazim Jewish ancestry and one of Chinese ancestry. The data come from 12 technologies: BioNano Genomics, Complete Genomics paired-end and LFR, Ion Proton exome, Oxford Nanopore, Pacific Biosciences, SOLiD, 10X Genomics GemCode WGS, and Illumina exome and WGS paired-end, mate-pair, and synthetic long reads. Cell lines, DNA, and data from these individuals are publicly available. Therefore, we expect these data to be useful for revealing novel information about the human genome and improving sequencing technologies, SNP, indel, and structural variant calling, and de novo assembly.
              • Record: found
              • Abstract: found
              • Article: found
              Is Open Access

              Expansion of the Human Phenotype Ontology (HPO) knowledge base and resources

              Abstract The Human Phenotype Ontology (HPO)—a standardized vocabulary of phenotypic abnormalities associated with 7000+ diseases—is used by thousands of researchers, clinicians, informaticians and electronic health record systems around the world. Its detailed descriptions of clinical abnormalities and computable disease definitions have made HPO the de facto standard for deep phenotyping in the field of rare disease. The HPO’s interoperability with other ontologies has enabled it to be used to improve diagnostic accuracy by incorporating model organism data. It also plays a key role in the popular Exomiser tool, which identifies potential disease-causing variants from whole-exome or whole-genome sequencing data. Since the HPO was first introduced in 2008, its users have become both more numerous and more diverse. To meet these emerging needs, the project has added new content, language translations, mappings and computational tooling, as well as integrations with external community data. The HPO continues to collaborate with clinical adopters to improve specific areas of the ontology and extend standardized disease descriptions. The newly redesigned HPO website (www.human-phenotype-ontology.org) simplifies browsing terms and exploring clinical features, diseases, and human genes.

                Author and article information

                Journal
                9815831
                22061
                Genet Med
                Genet Med
                Genetics in medicine : official journal of the American College of Medical Genetics
                1098-3600
                1530-0366
                14 February 2025
                January 2025
                10 October 2024
                21 February 2025
                : 27
                : 1
                : 101292
                Affiliations
                [1 ]The Jackson Laboratory for Genomic Medicine, Farmington, CT
                [2 ]William Harvey Research Institute, Queen Mary University of London, London, United Kingdom
                [3 ]Berlin Institute of Health, Charité-Universitätsmedizin Berlin, Berlin, Germany
                Author notes

                Author Contribution

                Conceptualization: P.N.R.; Data Curation: M.A.B., P.N.R.; Formal Analysis: M.A.B., Y.B., J.O.B.J., D.S., P.N.R.; Funding Acquisition: D.S., P.N.R.; Method: M.A.B., D.D., P.N.R.; Writing-original draft: M.A.B., P.N.R.; Writing-review and editing: M.A.B., D.D., Y.B., J.O.B.J., D.S., P.N.R.

                [* ]Correspondence and requests for materials should be addressed to Peter N. Robinson, The Jackson Laboratory for Genomic Medicine, 10 Discovery Drive, Farmington, CT 6032. peter.robinson@ 123456jax.org ; peter.robinson@ 123456bih-charite.de
                Author information
                http://orcid.org/0000-0002-0736-9199
                Article
                NIHMS2053850
                10.1016/j.gim.2024.101292
                11843448
                39396132
                e4c723e8-d78a-47f1-a72f-16e88405c62d

                This is an open access article under the CC BY license ( http://creativecommons.org/licenses/by/4.0/).

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                Categories
                Article

                Genetics
                genomic diagnostics,human phenotype ontology,likelihood ratio,mendelian disease
                Genetics
                genomic diagnostics, human phenotype ontology, likelihood ratio, mendelian disease

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