Skip to content
View davidenoma's full-sized avatar
🎯
Focusing
🎯
Focusing
67 followers · 51 following

Achievements

Achievement: Pull SharkAchievement: Arctic Code Vault Contributor

Achievements

Achievement: Pull SharkAchievement: Arctic Code Vault Contributor

Highlights

  • Pro

Block or report davidenoma

Block user

Prevent this user from interacting with your repositories and sending you notifications. Learn more about blocking users.

You must be logged in to block users.

Please don't include any personal information such as legal names or email addresses. Maximum 100 characters, markdown supported. This note will be visible to only you.
Report abuse

Contact GitHub support about this user’s behavior. Learn more about reporting abuse.

Report abuse
davidenoma/README.md
  • 👀 I research Machine Learning, Artificial intelligence, Statistical Genetics and Bioinformatics. This is applied to Genetics & Precision Medicine of Neuropsychiatric disorders, Cancers and Polygenic risk prediction.
  • 👨🏽‍💻 I write Python, R, Java, PHP, Bash, SQL, HTML and associated frameworks and libraries
  • 🚀 I build web, mobile, bioinformatics & data platforms and products.
  • 🌱 I’m currently learning Representation learning and Data engineering pipelines cloud platforms.
  • 💞️ I want to collaborate and consult on machine learning, data science and bioinformatics projects.
  • 📫 How to reach me davidenoma@gmail.com

Pinned Loading

  1. R-Language-scripts R-Language-scripts Public

    Comprehensive collection of scripts and pipelines in R for Bioinformatics & general use. Includes, R fundamentals, bayesian statistics, cancer genomics, data analysis, genomic analysis and targeted…

    R 9

  2. xMLGenoRisk xMLGenoRisk Public

    Machine Learning approach for genetic risk prediction. I applied a modified, XGBoost algorithm and an iterative SNP selection algorithm to find the top features (SNPs) that best predict the risk of…

    Jupyter Notebook 7 2

  3. DEMON-NEUROHACK/Challenge-1-London-Team-B-Genome-Wide-Association-Lovers- DEMON-NEUROHACK/Challenge-1-London-Team-B-Genome-Wide-Association-Lovers- Public

    We suggest a novel way of defining NCD as a continuous phenotype, and we employ a mixed linear model to account for pronounced population stratification in the South Asian sample, which is more div…

    HTML 6

  4. collaborativebioinformatics/Disease_subsetting collaborativebioinformatics/Disease_subsetting Public

    Colorectal cancer CMs subtyping and personalized medication recommendation based on RNA seq pathway analysis

    Jupyter Notebook 9 2

  5. breast-cancer-risk-prediction breast-cancer-risk-prediction Public

    Forked from hambeh/breast-cancer-risk-prediction

    Breast cancer risk prediction using genotyped data

    Python 1

  6. PRS_reporting PRS_reporting Public

    Forked from collaborativebioinformatics/PRS_reporting

    Clinical Reporting of Polygenic Risk Scores

    Jupyter Notebook 1