challengingclockuniversality
Challenging Clock Universality: A Comprehensive Analysis of Tissue-Specific Methylation Patterns in Mammalian Epigenetic Clocks
Science Score: 44.0%
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Low similarity (0.8%) to scientific vocabulary
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Repository
Challenging Clock Universality: A Comprehensive Analysis of Tissue-Specific Methylation Patterns in Mammalian Epigenetic Clocks
Basic Info
Statistics
- Stars: 0
- Watchers: 1
- Forks: 0
- Open Issues: 0
- Releases: 2
Created about 2 years ago
· Last pushed about 1 year ago
Metadata Files
Readme
Citation
README.md
MScProjectScripts
Scripts and files associated to the MSc Thesis: "Challenging Clock Universality: A Comprehensive Analysis of Tissue-Specific Methylation Patterns in Mammalian Epigenetic Clocks"
Owner
- Name: Catia Antunes
- Login: AntunesCSR
- Kind: user
- Location: Reading, UK
- Company: University of Reading
- Repositories: 1
- Profile: https://github.com/AntunesCSR
Citation (CITATION.cff)
cff-version: 1.2.0
message: "If you use this software, please cite it as below."
authors:
- family-names: "Antunes"
given-names: "Cátia"
title: "Challenging Clock Universality Repository"
version: 1.0.0
date-released: 2024-09-01 # Replace with the actual release date
url: "https://github.com/AntunesCSR/ChallengingClockUniversality"
type: software
keywords:
- bioinformatics
- epigenetic clock
- aging
license: MIT License
repository-code: "https://github.com/AntunesCSR/ChallengingClockUniversality"
abstract: "This repository houses the computational framework and comprehensive analysis developed for a Master's thesis
in Bioinformatics. The research focuses on critically examining the universality principle of the pan-mammalian epigenetic clocks, a key
concept in the field of aging biology. Through statistical analyses and computational approaches, this
work challenges existing paradigms and explores the tissue-specific nature of epigenetic aging markers. The repository
includes custom Python scripts, R notebooks, and data processing pipelines designed to interrogate methylation
datasets across diverse tissue types. This research contributes to the ongoing scientific discourse on the
mechanisms of biological aging and the development of more accurate, context-specific epigenetic biomarkers."
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