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    • FREEC

      Public
      Control-FREEC: Copy number and genotype annotation in whole genome and whole exome sequencing data
      C++
      491478710Updated Aug 22, 2024Aug 22, 2024
    • Python
      BSD 3-Clause "New" or "Revised" License
      0150Updated Jul 16, 2024Jul 16, 2024
    • survboard

      Public
      R
      MIT License
      0620Updated Jul 15, 2024Jul 15, 2024
    • Infer copy number variation (CNV) from scRNA-seq data. Plays nicely with Scanpy.
      Python
      BSD 3-Clause "New" or "Revised" License
      27101Updated May 21, 2024May 21, 2024
    • scalop

      Public
      Single Cell Analysis Operations
      R
      MIT License
      19000Updated May 16, 2024May 16, 2024
    • Jupyter Notebook
      0000Updated Apr 29, 2024Apr 29, 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
      MIT License
      0000Updated Feb 20, 2024Feb 20, 2024
    • CHIPIN

      Public
      ChIP-seq Intersample Normalization
      R
      GNU General Public License v3.0
      6731Updated Feb 1, 2024Feb 1, 2024
    • More data, more problems? On noise resistance in multi-omics cancer survival models
      Python
      MIT License
      1600Updated Jul 29, 2023Jul 29, 2023
    • CanSig

      Public
      Discovering de novo shared transcriptional programs in single cancer cells
      Python
      BSD 3-Clause "New" or "Revised" License
      312120Updated Jul 26, 2023Jul 26, 2023
    • HMCan

      Public
      C++
      4710Updated Jun 9, 2023Jun 9, 2023
    • Teaching

      Public
      Teaching materials
      Jupyter Notebook
      0200Updated May 16, 2023May 16, 2023
    • LILY

      Public
      Detection of super-enhancers in cancer data
      R
      92001Updated Apr 10, 2023Apr 10, 2023
    • This repository supplements the CanSig tool (https://github.com/boevaLab/cansig), providing additional information on performed experiments.
      Jupyter Notebook
      MIT License
      0100Updated Mar 27, 2023Mar 27, 2023
    • Python
      0000Updated Mar 9, 2023Mar 9, 2023
    • a package to simulate cancer single cells with joint CNV profiles based on Splatter
      Jupyter Notebook
      BSD 3-Clause "New" or "Revised" License
      1100Updated Jan 17, 2023Jan 17, 2023
    • This is the code collection for Hongzhe Li's Lab rotation project
      Jupyter Notebook
      0000Updated Jan 3, 2023Jan 3, 2023
    • latte

      Public
      Data analysis of latent representations
      Python
      MIT License
      1311Updated Dec 30, 2022Dec 30, 2022
    • ONCOCNV

      Public
      ONCOCNV - a package to detect copy number changes in Targeted Deep Sequencing and Exome-seq data
      R
      1224131Updated Nov 2, 2022Nov 2, 2022
    • TFCox

      Public
      Tensorflow implementation of the Cox Proportional Hazards model
      Jupyter Notebook
      0100Updated Jun 9, 2022Jun 9, 2022
    • Supporting code for the analysis in "Deciphering the etiology and role in oncogenic transformation of the CpG island methylator phenotype (CIMP): a pan-cancer analysis
      Jupyter Notebook
      MIT License
      1100Updated Feb 23, 2022Feb 23, 2022
    • Clonal reconstruction from HTS data
      R
      6000Updated Oct 26, 2021Oct 26, 2021
    • Python
      1100Updated Sep 2, 2021Sep 2, 2021
    • Jupyter Notebook
      0000Updated Nov 16, 2020Nov 16, 2020
    • Code for the CIMP in ACC paper
      1000Updated Apr 4, 2020Apr 4, 2020
    • sci

      Public
      Python
      Other
      6000Updated Mar 18, 2020Mar 18, 2020
    • SV-Bay

      Public
      Detection of structural variants in cancer mate-pair and paired-end data
      Python
      21240Updated May 3, 2019May 3, 2019
    • MasterTF

      Public
      Python
      1100Updated Aug 20, 2018Aug 20, 2018
    • ChIPseqReadSimulator: a tool to simulate ChIP-seq signal
      C++
      0000Updated Feb 14, 2017Feb 14, 2017