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Chris1221/README.md

Hi there, I'm Chris.

I am currently a lead scientist at Deep Genomics in Toronto. My work involves using machine learning and AI to identify causal drug targets from human genetics data. I previously completed my DPhil working with Gerton Lunter and Thomas Milne at the University of Oxford. Check out my website for a breakdown of previous projects and repositories of interest.

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  1. luntergroup/smcsmc Public

    Demographic inference from whole genomes

    C++ 11 4

  2. goldi Public

    R Package for Gene Ontology Label Discernment and Identification.

    R 7 2

  3. popsim-consortium/stdpopsim Public

    A library of standard population genetic models

    Python 133 93

  4. genomic_interval_pipeline Public

    Pre-processing of genomic intervals for deep learning.

    Rust

  5. yamldoc Public

    Dependency-free YAML documentation engine.

    Python 10 3

  6. LHentges/LanceOtron Public

    Python 25 4

518 contributions in the last year

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Activity overview

Contributed to Chris1221/wdlfmt, Chris1221/Chris1221, Chris1221/yamldoc and 1 other repository
Loading A graph representing Chris1221's contributions from March 24, 2024 to March 24, 2025. The contributions are 57% commits, 25% code review, 18% pull requests, 0% issues.

Contribution activity

March 2025

19 contributions in private repositories Mar 4 – Mar 23
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