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    • Graph augmentation strategies for self-supervised pretraining of graph neural networks in spatial omics
      Python
      0155Updated Oct 26, 2025Oct 26, 2025
    • CanSig: a package to compare methods for discovering shared transcriptional states in cancer.
      Jupyter Notebook
      0210Updated Oct 10, 2025Oct 10, 2025
    • Python
      01000Updated Oct 3, 2025Oct 3, 2025
    • Jupyter Notebook
      0000Updated Oct 1, 2025Oct 1, 2025
    • ANS_signature_scoring: A gene expression signature scoring Python package.
      Python
      31610Updated Sep 20, 2025Sep 20, 2025
    • CancerFoundation: A single-cell RNA sequencing foundation model to decipher drug resistance in cancer
      Jupyter Notebook
      42510Updated Sep 12, 2025Sep 12, 2025
    • survboard

      Public
      Python
      0700Updated Aug 1, 2025Aug 1, 2025
    • Jupyter Notebook
      1000Updated Jul 28, 2025Jul 28, 2025
    • UniversalEPI: Harnessing Attention Mechanisms to Decode Chromatin Interactions in Rare and Unexplored Cell Types
      Jupyter Notebook
      0400Updated Jul 19, 2025Jul 19, 2025
    • Jupyter Notebook
      0000Updated Jul 17, 2025Jul 17, 2025
    • Jupyter Notebook
      7001Updated Jul 8, 2025Jul 8, 2025
    • Python
      0000Updated Jul 2, 2025Jul 2, 2025
    • ASAP

      Public
      Early feature extraction determines performance: systematic evaluation of deep learning models for high-resolution chromatin accessibility prediction
      Python
      1210Updated Jun 17, 2025Jun 17, 2025
    • CDState

      Public
      Python
      0100Updated May 13, 2025May 13, 2025
    • Repository containing all the code necessary for reproducing the paper "Filtering cells with high mitochondrial content removes viable metabolically altered malignant cell populations in cancer single-cell studies" (Yates, Kraft, and Boeva)
      Jupyter Notebook
      1100Updated Mar 18, 2025Mar 18, 2025
    • HTML
      40000Updated Dec 19, 2024Dec 19, 2024
    • Benchmarking Self-Supervised Learning for Single-Cell Data
      Python
      0600Updated Oct 28, 2024Oct 28, 2024
    • FREEC

      Public
      Control-FREEC: Copy number and genotype annotation in whole genome and whole exome sequencing data
      C++
      511729310Updated Aug 22, 2024Aug 22, 2024
    • Python
      1371Updated Jul 16, 2024Jul 16, 2024
    • Infer copy number variation (CNV) from scRNA-seq data. Plays nicely with Scanpy.
      Python
      30102Updated May 21, 2024May 21, 2024
    • scalop

      Public
      Single Cell Analysis Operations
      R
      26100Updated May 16, 2024May 16, 2024
    • 0000Updated Apr 15, 2024Apr 15, 2024
    • CRCPolyp

      Public
      Supporting code for Identification of early DNA methylation field cancerization in normal colonic mucosa in patients with adenomas and neoplastic lesions
      Jupyter Notebook
      0000Updated Feb 20, 2024Feb 20, 2024
    • CHIPIN

      Public
      ChIP-seq Intersample Normalization
      R
      5851Updated Feb 1, 2024Feb 1, 2024
    • More data, more problems? On noise resistance in multi-omics cancer survival models
      Python
      2900Updated Jul 29, 2023Jul 29, 2023
    • HMCan

      Public
      C++
      3710Updated Jun 9, 2023Jun 9, 2023
    • Teaching

      Public
      Teaching materials
      Jupyter Notebook
      0500Updated May 16, 2023May 16, 2023
    • LILY

      Public
      Detection of super-enhancers in cancer data
      R
      92101Updated Apr 10, 2023Apr 10, 2023
    • This repository supplements the CanSig tool (https://github.com/boevaLab/cansig), providing additional information on performed experiments.
      Jupyter Notebook
      0100Updated Mar 27, 2023Mar 27, 2023
    • a package to simulate cancer single cells with joint CNV profiles based on Splatter
      Jupyter Notebook
      1100Updated Jan 17, 2023Jan 17, 2023