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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。

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

作者信息

Dilliott Allison A, Costanzo Maria C, Bandres-Ciga Sara, Blauwendraat Cornelis, Casey Bradford, Hoang Quy, Iwaki Hirotaka, Jang Dongkeun, Kim Jonggeol Jeffrey, Leonard Hampton L, Levine Kristin S, Makarious Mary, Nguyen Trang T, Rouleau Guy A, Singleton Andrew B, Smadbeck Patrick, Solle J, Vitale Dan, Nalls Mike, Flannick Jason, Burtt Noël P, Farhan Sali M K

机构信息

Department of Neurology and Neurosurgery, McGill University, Montreal, Quebec, Canada.

Montreal Neurological Institute-Hospital, McGill University, Montreal, Quebec, Canada.

出版信息

Neurol Genet. 2025 Feb 21;11(2):e200246. doi: 10.1212/NXG.0000000000200246. eCollection 2025 Apr.

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.

摘要

尽管大规模基因关联研究已被证明有助于描绘神经退行性疾病的进程,但我们仍未完全了解这些疾病的病理机制,这导致合适的治疗选择很少且存在诊断难题。为了弥补这些差距,神经退行性疾病知识门户(NDKP)作为一项开放科学倡议而创建,旨在汇总、便于分析并展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保密性。该门户包含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,其中包括阿尔茨海默病、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,以有效利用这些数据集,并协助促进定制的基因组分析。在此,我们总结了目前包含在门户中的基因组数据集、数据集的生物信息学处理以及所捕获的各种表型。我们还展示了各种用户界面和集成分析工具的示例用例,以证明它们在为基因组学专家和其他学科人员从源头上提取高质量结果方面具有广泛的实用性。总体而言,NDKP促进开放科学与合作,最大限度地挖掘研究人员和联盟投入大量资源所产生的大规模数据集的发现潜力,并得出可重复的结论,以改善神经退行性疾病患者的诊断和治疗护理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d425/11849525/cc0e47ea3612/NXG-2024-100157f1.jpg

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