m+Medelevator.RU
← Поиск публикаций
Nature genetics · 2023

PhenoScore quantifies phenotypic variation for rare genetic diseases by combining facial analysis with other clinical features using a machine-learning framework.

СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод пока не подготовлен
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…

История · было → стало

Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.

Dingemans Alexander J M, Hinne Max, Truijen Kim M G, Goltstein Lia, van Reeuwijk Jeroen, de Leeuw Nicole, Schuurs-Hoeijmakers Janneke, Pfundt Rolph, Diets Illja J, den Hoed Joery, de Boer Elke, Coenen-van der Spek Jet, Jansen Sandra, van Bon Bregje W, Jonis Noraly, Ockeloen Charlotte W, Vulto-van Silfhout Anneke T, Kleefstra Tjitske, Koolen David A, Campeau Philippe M, Palmer Elizabeth E, Van Esch Hilde, Lyon Gholson J, Alkuraya Fowzan S, Rauch Anita, Marom Ronit, Baralle Diana, van der Sluijs Pleuntje J, Santen Gijs W E, Kooy R Frank, van Gerven Marcel A J, Vissers Lisenka E L M, de Vries Bert B A

Аннотация

Several molecular and phenotypic algorithms exist that establish genotype-phenotype correlations, including facial recognition tools. However, no unified framework that investigates both facial data and other phenotypic data directly from individuals exists. We developed PhenoScore: an open-source, artificial intelligence-based phenomics framework, combining facial recognition technology with Human Phenotype Ontology data analysis to quantify phenotypic similarity. Here we show PhenoScore's ability to recognize distinct phenotypic entities by establishing recognizable phenotypes for 37 of 40 investigated syndromes against clinical features observed in individuals with other neurodevelopmental disorders and show it is an improvement on existing approaches. PhenoScore provides predictions for individuals with variants of unknown significance and enables sophisticated genotype-phenotype studies by testing hypotheses on possible phenotypic (sub)groups. PhenoScore confirmed previously known phenotypic subgroups caused by variants in the same gene for SATB1, SETBP1 and DEAF1 and provides objective clinical evidence for two distinct ADNP-related phenotypes, already established functionally.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты