自动检测大型群组中的单亲畸形。

IF 3.8 2区 生物学 Q2 GENETICS & HEREDITY
Human Genetics Pub Date : 2024-08-01 Epub Date: 2024-07-16 DOI:10.1007/s00439-024-02687-w
Johanna Moch, Maximilian Radtke, Thomas Liehr, Thomas Eggermann, Christian Gilissen, Rolph Pfundt, Galuh Astuti, Julia Hentschel, Isabell Schumann
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引用次数: 0

摘要

单亲裂殖(UPD)是指染色体的两个同源染色体仅由父母一方遗传。在测序数据中检测 UPD 尚不成熟,这也是基因诊断中的一个常见缺陷。我们应用内部的 UPD 检测管道评估了一组 9212 个样本,包括多基因面板以及单人、双人或三人组的外显子组测序数据。我们利用这些结果来设计我们的公开网络应用 AltAFplotter。通过微卫星、多重连接依赖性探针扩增以及桑格测序,我们确定并验证了被归类为异位二体、全染色体或节段性等位二体的 UPDs。我们在 22 号染色体上发现了 14 个以前未诊断出的 UPD,包括 9 个等位二体、4 个节段性等位二体和 1 个异位二体。我们通过同卵致病变体或印记紊乱,将其中 8 项结果定性为潜在致病因素。总之,我们的研究证明了我们的 UPD 检测管道与我们的网络应用程序 altAFplotter 在可靠识别 UPD 方面的实用性。这不仅提高了对生长和代谢紊乱以及发育迟缓病例的诊断率,还增强了对可能与复发风险和遗传咨询相关的 UPDs 的了解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Automatized detection of uniparental disomies in a large cohort.

Automatized detection of uniparental disomies in a large cohort.

Uniparental disomy (UPD) is the inheritance of both homologues of a chromosome from only one parent. The detection of UPDs in sequencing data is not well established and a common gap in genetic diagnostics. We applied our in-house UPD detection pipeline to evaluate a cohort of 9212 samples, including multigene panels as well as exome sequencing data in a single, duo or trio constellation. We used the results to inform the design of our publicly available web app altAFplotter. UPDs categorized as heterodisomy, whole chromosome or segmental isodisomy were identified and validated with microsatellites, multiplex ligation-dependent probe amplification as well as Sanger sequencing. We detected 14 previously undiagnosed UPDs including nine isodisomies, four segmental isodisomies as well as one heterodisomy on chromosome 22. We characterized eight findings as potentially causative through homozygous pathogenic variants or imprinting disorders. Overall, our study demonstrates the utility of our UPD detection pipeline with our web app, altAFplotter, to reliably identify UPDs. This not only increases the diagnostic yield of cases with growth and metabolic disturbances, as well as developmental delay, but also enhances the understanding of UPDs that may be relevant for recurrence risks and genetic counseling.

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来源期刊
Human Genetics
Human Genetics 生物-遗传学
CiteScore
10.80
自引率
3.80%
发文量
94
审稿时长
1 months
期刊介绍: Human Genetics is a monthly journal publishing original and timely articles on all aspects of human genetics. The Journal particularly welcomes articles in the areas of Behavioral genetics, Bioinformatics, Cancer genetics and genomics, Cytogenetics, Developmental genetics, Disease association studies, Dysmorphology, ELSI (ethical, legal and social issues), Evolutionary genetics, Gene expression, Gene structure and organization, Genetics of complex diseases and epistatic interactions, Genetic epidemiology, Genome biology, Genome structure and organization, Genotype-phenotype relationships, Human Genomics, Immunogenetics and genomics, Linkage analysis and genetic mapping, Methods in Statistical Genetics, Molecular diagnostics, Mutation detection and analysis, Neurogenetics, Physical mapping and Population Genetics. Articles reporting animal models relevant to human biology or disease are also welcome. Preference will be given to those articles which address clinically relevant questions or which provide new insights into human biology. Unless reporting entirely novel and unusual aspects of a topic, clinical case reports, cytogenetic case reports, papers on descriptive population genetics, articles dealing with the frequency of polymorphisms or additional mutations within genes in which numerous lesions have already been described, and papers that report meta-analyses of previously published datasets will normally not be accepted. The Journal typically will not consider for publication manuscripts that report merely the isolation, map position, structure, and tissue expression profile of a gene of unknown function unless the gene is of particular interest or is a candidate gene involved in a human trait or disorder.
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