The Neurodegenerative Disease Knowledge Portal: Propelling Discovery Through the Sharing of Neurodegenerative Disease Genomic Resources.

IF 3 3区 医学 Q2 CLINICAL NEUROLOGY
Neurology-Genetics Pub Date : 2025-02-21 eCollection Date: 2025-04-01 DOI:10.1212/NXG.0000000000200246
Allison A Dilliott, Maria C Costanzo, Sara Bandres-Ciga, Cornelis Blauwendraat, Bradford Casey, Quy Hoang, Hirotaka Iwaki, Dongkeun Jang, Jonggeol Jeffrey Kim, Hampton L Leonard, Kristin S Levine, Mary Makarious, Trang T Nguyen, Guy A Rouleau, Andrew B Singleton, Patrick Smadbeck, J Solle, Dan Vitale, Mike Nalls, Jason Flannick, Noël P Burtt, Sali M K Farhan
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引用次数: 0

Abstract

Although large-scale genetic association studies have proven useful for the delineation of neurodegenerative disease processes, we still lack a full understanding of the pathologic mechanisms of these diseases, resulting in few appropriate treatment options and diagnostic challenges. To mitigate these gaps, the Neurodegenerative Disease Knowledge Portal (NDKP) was created as an open-science initiative with the aim to aggregate, enable analysis, and display all available genomic datasets of neurodegenerative disease, while protecting the integrity and confidentiality of the underlying datasets. The portal contains 218 genomic datasets, including genotyping and sequencing studies, of individuals across 10 different phenotypic groups, including neurologic conditions such as Alzheimer disease, amyotrophic lateral sclerosis, Lewy body dementia, and Parkinson disease. In addition to securely hosting large genomic datasets, the NDKP provides accessible workflows and tools to effectively use the datasets and assist in the facilitation of customized genomic analyses. Here, we summarize the genomic datasets currently included within the portal, the bioinformatics processing of the datasets, and the variety of phenotypes captured. We also present example use cases of the various user interfaces and integrated analytic tools to demonstrate their extensive utility in enabling the extraction of high-quality results at the source, for both genomics experts and those in other disciplines. Overall, the NDKP promotes open science and collaboration, maximizing the potential for discovery from the large-scale datasets researchers and consortia are expending immense resources to produce and resulting in reproducible conclusions to improve diagnostic and therapeutic care for patients with neurodegenerative disease.

神经退行性疾病知识门户:通过共享神经退行性疾病基因组资源推动发现。
尽管大规模的遗传关联研究已被证明对描述神经退行性疾病的过程是有用的,但我们仍然缺乏对这些疾病的病理机制的充分理解,导致很少有适当的治疗选择和诊断挑战。为了缓解这些差距,神经退行性疾病知识门户(NDKP)被创建为一项开放科学倡议,旨在汇总、分析和显示所有可用的神经退行性疾病基因组数据集,同时保护基础数据集的完整性和机密性。该门户网站包含218个基因组数据集,包括基因分型和测序研究,涉及10个不同表型组的个体,包括阿尔茨海默病、肌萎缩侧索硬化症、路易体痴呆和帕金森病等神经系统疾病。除了安全托管大型基因组数据集外,NDKP还提供可访问的工作流程和工具,以有效使用数据集并协助促进定制基因组分析。在这里,我们总结了目前包含在门户网站中的基因组数据集,数据集的生物信息学处理以及捕获的各种表型。我们还提供了各种用户界面和集成分析工具的示例用例,以展示它们在从源头提取高质量结果方面的广泛实用性,适用于基因组学专家和其他学科的专家。总体而言,NDKP促进开放科学和合作,最大限度地发挥从大规模数据集中发现的潜力,研究人员和联盟正在花费大量资源来得出可重复的结论,以改善神经退行性疾病患者的诊断和治疗护理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Neurology-Genetics
Neurology-Genetics Medicine-Neurology (clinical)
CiteScore
6.30
自引率
3.20%
发文量
107
审稿时长
15 weeks
期刊介绍: Neurology: Genetics is an online open access journal publishing peer-reviewed reports in the field of neurogenetics. Original articles in all areas of neurogenetics will be published including rare and common genetic variation, genotype-phenotype correlations, outlier phenotypes as a result of mutations in known disease-genes, and genetic variations with a putative link to diseases. This will include studies reporting on genetic disease risk and pharmacogenomics. In addition, Neurology: Genetics will publish results of gene-based clinical trials (viral, ASO, etc.). Genetically engineered model systems are not a primary focus of Neurology: Genetics, but studies using model systems for treatment trials are welcome, including well-powered studies reporting negative results.
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