Construction of A Dataset for All Expressed Transcripts for Alzheimer’s Disease Research DOI Creative Commons
Zhenyu Huang,

Bocheng Shi,

Xuechen Mu

и другие.

Brain Sciences, Год журнала: 2024, Номер 14(12), С. 1180 - 1180

Опубликована: Ноя. 25, 2024

Accurate identification and functional annotation of splicing isoforms non-coding RNAs (lncRNAs), alongside full-length protein-encoding transcripts, are critical for understanding gene (mis)regulation metabolic reprogramming in Alzheimer’s disease (AD). This study aims to provide a comprehensive accurate transcriptome resource improve existing AD transcript databases. Background/Objectives: Gene mis-regulation play key role AD, yet databases lack lncRNAs. generate refined dataset, expanding the onset progression. Methods: Publicly available RNA-seq data from pre-AD tissues were utilized. Advanced bioinformatics tools applied assemble annotate including lncRNAs, with an emphasis on correcting errors enhancing accuracy. Results: A significantly improved dataset was generated, which includes detailed annotations expands scope provides new insights into molecular mechanisms underlying AD. The findings demonstrate that captures more relevant details about progression compared publicly data. Conclusions: newly developed associated analysis offer valuable contribution research, providing deeper disease’s mechanisms. work supports future research regulation serves as foundation exploring novel therapeutic targets.

Язык: Английский

Elucidating the Functional Roles of Long Non-coding RNAs in Alzheimer's Disease DOI Open Access
Zhenyu Huang,

Qiufen Chen,

Xuechen Mu

и другие.

Опубликована: Июль 10, 2024

Alzheimer's disease (AD) is a multifaceted neurodegenerative disorder characterized by cognitive decline and neuronal loss, representing most challenging health issue. We present computational analysis of transcriptomic data AD tissues vs. healthy controls, focused on elucidation functional roles played long non-coding RNAs (lncRNAs) throughout the progression. first assembled our own lncRNA transcripts from raw RNA-Seq generated 527 samples dorsolateral prefrontal cortex, resulting in identification 31,574 novel genes. Based co-expression analyses between mRNAs lncRNAs, network constructed. Maximal subnetworks with dense connections are identified as clusters. Pathway enrichment conducted over lncRNAs each cluster, which serve basis for inference involved key steps an development model that we have previously build based protein-encoding Detailed information presented about activities related to stress response, reprogrammed metabolism, cell-polarity, development. Our also revealed discerning power distinguishing stage controls. This study represents its kind.

Язык: Английский

Процитировано

4

Optimizing Model Performance and Interpretability: Application to Biological Data Classification DOI Open Access
Zhenyu Huang,

Xuechen Mu,

Yangkun Cao

и другие.

Genes, Год журнала: 2025, Номер 16(3), С. 297 - 297

Опубликована: Фев. 28, 2025

This study introduces a novel framework that simultaneously addresses the challenges of performance accuracy and result interpretability in transcriptomic-data-based classification. Background/objectives: In biological data classification, it is challenging to achieve both high at same time. presents address The goal select features, models, meta-voting classifier optimizes classification interpretability. Methods: consists four-step feature selection process: (1) identification metabolic pathways whose enzyme-gene expressions discriminate samples with different labels, aiding interpretability; (2) expression variance largely captured by first principal component gene matrix; (3) minimal sets genes, collective discerning power covers 95% pathway-based power; (4) introduction adversarial identify filter genes sensitive such samples. Additionally, are used optimal model, constructed based on optimized model results. Results: applied two cancer problems showed binary prediction was comparable full-gene F1-score differences between −5% 5%. ternary significantly better, ranging from −2% 12%, while also maintaining excellent selected genes. Conclusions: effectively integrates selection, sample handling, optimization, offering valuable tool for wide range problems. Its ability balance makes highly applicable field computational biology.

Язык: Английский

Процитировано

0

A Map of Transcriptomic Signatures of Different Brain Areas in Alzheimer’s Disease DOI Open Access
Riccardo Rocco Ferrari, Valentina Fantini, Maria Garofalo

и другие.

International Journal of Molecular Sciences, Год журнала: 2024, Номер 25(20), С. 11117 - 11117

Опубликована: Окт. 16, 2024

Alzheimer’s disease (AD) is a neurodegenerative disorder that progressively involves brain regions with an often-predictable pattern. Damage to the appears spread and worsen time, but molecular mechanisms underlying region-specific distribution of AD pathology at different stages are still under-investigated. In this study, whole-transcriptome analysis was carried out on samples from hippocampus (HI), temporal parietal cortices (TC PC, respectively), cingulate cortex (CG), substantia nigra (SN) six subjects definite diagnosis three healthy age-matched controls in duplicate. The transcriptomic results showed greater number differentially expressed genes (DEGs) TC (1571) CG (1210) smaller DEGs HI (206), PC (109), SN (60). Furthermore, GSEA difference between group areas affected early (HI TC) were subsequently involved (PC, CG, SN). Notably, TC, there significant downregulation shared primarily synaptic transmission, while SN, protein folding trafficking. course could follow time- severity-related pattern arises misfolding, as observed leads impairment, TC. Therefore, map biological processes pathogenesis may be traced. This aid discovery novel targets order develop effective well-timed therapeutic approaches.

Язык: Английский

Процитировано

2

Construction of A Dataset for All Expressed Transcripts for Alzheimer’s Disease Research DOI Creative Commons
Zhenyu Huang,

Bocheng Shi,

Xuechen Mu

и другие.

Brain Sciences, Год журнала: 2024, Номер 14(12), С. 1180 - 1180

Опубликована: Ноя. 25, 2024

Accurate identification and functional annotation of splicing isoforms non-coding RNAs (lncRNAs), alongside full-length protein-encoding transcripts, are critical for understanding gene (mis)regulation metabolic reprogramming in Alzheimer’s disease (AD). This study aims to provide a comprehensive accurate transcriptome resource improve existing AD transcript databases. Background/Objectives: Gene mis-regulation play key role AD, yet databases lack lncRNAs. generate refined dataset, expanding the onset progression. Methods: Publicly available RNA-seq data from pre-AD tissues were utilized. Advanced bioinformatics tools applied assemble annotate including lncRNAs, with an emphasis on correcting errors enhancing accuracy. Results: A significantly improved dataset was generated, which includes detailed annotations expands scope provides new insights into molecular mechanisms underlying AD. The findings demonstrate that captures more relevant details about progression compared publicly data. Conclusions: newly developed associated analysis offer valuable contribution research, providing deeper disease’s mechanisms. work supports future research regulation serves as foundation exploring novel therapeutic targets.

Язык: Английский

Процитировано

1