Wiki source code of Neurodiagnoses

Version 7.2 by manuelmenendez on 2025/01/27 23:22

Show last authors
1 (% class="jumbotron" %)
2 (((
3 (% class="container" %)
4 (((
5 = //A new tridimensional diagnostic framework for CNS conditions// =
6
7 This project is focused on developing a novel nosological and diagnostic framework for neurological diseases by using advanced AI techniques and integrating data from neuroimaging, biomarkers, and biomedical ontologies.
8 We aim to create a structured, interpretable, and scalable diagnostic tool.
9 )))
10 )))
11
12 (% class="row" %)
13 (((
14 (% class="col-xs-12 col-sm-8" %)
15 (((
16 = What is this about and what can I find here? =
17
18 ==== **Overview** ====
19
20 The //Tridimensional Diagnostic Framework// redefines how neurodegenerative diseases (NDDs) are classified by focusing on:
21
22 * **Axis 1**: Etiology (genetic/sporadic and environmental factors).
23 * **Axis 2**: Molecular Markers (biomarkers and proteinopathies).
24 * **Axis 3**: Neuroanatomoclinical correlations (linking clinical symptoms to structural changes in the nervous system).
25
26 This methodology enables:
27
28 * Greater precision in diagnosis.
29 * Integration of incomplete datasets using AI-driven probabilistic modeling.
30 * Stratification of patients for personalized treatment.
31
32 ==== **Diagnostic Axes** ====
33
34 * (((
35 **Axis 1: Etiology**
36
37 * //Description//: Focuses on genetic and sporadic causes, identifying risk factors and potential triggers.
38 * //Examples//: APOE ε4 as a genetic risk factor, or cardiovascular health affecting NDD progression.
39 * //Tests//: Genetic testing, lifestyle and cardiovascular screening.
40 )))
41 * (((
42 **Axis 2: Molecular Markers**
43
44 * //Description//: Analyzes primary (amyloid-beta, tau) and secondary biomarkers (NFL, GFAP) for tracking disease progression.
45 * //Examples//: CSF amyloid-beta concentrations to confirm Alzheimer’s pathology.
46 * //Tests//: Blood/CSF biomarkers, PET imaging (Tau-PET, Amyloid-PET).
47 )))
48 * (((
49 **Axis 3: Neuroanatomoclinical**
50
51 * //Description//: Links clinical symptoms to neuroanatomical changes, such as atrophy or functional impairments.
52 * //Examples//: Hippocampal atrophy correlating with memory deficits.
53 * //Tests//: MRI volumetrics, FDG-PET, neuropsychological evaluations.
54 )))
55
56 ==== **Applications** ====
57
58 This system enhances:
59
60 * **Research**: By stratifying patients, reduces cohort heterogeneity in clinical trials.
61 * **Clinical Practice**: Provides dynamic diagnostic annotations with timestamps for longitudinal tracking.
62
63 == Who has access? ==
64
65 We welcome contributions from the global community. Let’s build the future of neurological diagnostics together!
66
67 == How to Contribute: ==
68
69 * Access the `/docs` folder for guidelines.
70 * Use `/code` for the latest AI pipelines.
71 * Share feedback and ideas in the wiki discussion pages.
72
73 == Key Objectives: ==
74
75 * Develop interpretable AI models for diagnosis and progression tracking.
76 * Integrate data from Human Phenotype Ontology (HPO), Gene Ontology (GO), and other biomedical resources.
77 * Foster collaboration among neuroscientists, AI researchers, and clinicians.
78 )))
79
80
81 (% class="col-xs-12 col-sm-4" %)
82 (((
83 {{box title="**Contents**"}}
84 {{toc/}}
85 {{/box}}
86
87 == Main contents: ==
88
89 * `/docs`: Documentation and contribution guidelines.
90 * `/code`: Machine learning pipelines and scripts.
91 * `/data`: Sample datasets for testing.
92 * `/outputs`: Generated models, visualizations, and reports.
93 )))
94 )))