Interdisciplinary PSP Bioinformatics and Neuroinformatics (BNP), School of Science and Technology, Hellenic Open University, Patras, Greece.
Bioinformatics and Human Electrophysiology Lab (BiHELab), Department of Informatics, Ionian University, Corfu, Greece.
Adv Exp Med Biol. 2023;1423:251-256. doi: 10.1007/978-3-031-31978-5_25.
The development in the field of biomedical technology has brought significant progress in the diagnosis and prediction of many complex diseases. Part of this development is the single-cell RNA sequencing analysis, which allows the study of a complex disease in great depth at the cellular level. Such analyses can decipher the mechanisms that cause complex diseases, such as Alzheimer's disease (AD). However, the increasing depth in the collection of single-cell RNA sequencing data implies, in addition to greater challenges, the production of a large amount of information, which needs careful analysis. Toward this direction, we examine the approach to single-cell RNA sequencing data through the development of an exploratory data analysis methodology. For this purpose, a combination of various tools is presented for their effective and efficient processing. At the same time, reference is made to the relevant biological concepts, the goals and challenges of the studies, and the workflows of sequencing, preprocessing, and analysis of the data. Our framework is applied to Alzheimer's disease data providing evidence that such data are quite complex while the appropriate preprocess step can boost the machine learning processes for identifying AD signatures.
生物医学技术领域的发展在许多复杂疾病的诊断和预测方面带来了重大进展。其中一部分发展是单细胞 RNA 测序分析,它允许在细胞水平上深入研究复杂疾病。这种分析可以揭示导致复杂疾病的机制,如阿尔茨海默病 (AD)。然而,单细胞 RNA 测序数据的采集深度不断增加,不仅带来了更大的挑战,还产生了大量需要仔细分析的信息。为此,我们通过开发探索性数据分析方法来研究单细胞 RNA 测序数据。为此,提出了各种工具的组合,以实现其有效和高效的处理。同时,还参考了相关的生物学概念、研究的目标和挑战,以及测序、预处理和数据分析的工作流程。我们的框架应用于阿尔茨海默病数据,证明了这些数据非常复杂,而适当的预处理步骤可以增强机器学习过程,以识别 AD 特征。