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    • Germline WGS variant calling across cancer types
      WDL
      GNU General Public License v2.0
      0001Updated Oct 11, 2024Oct 11, 2024
    • Underlying content for the Molecular Oncology Almanac's database
      GNU General Public License v2.0
      1500Updated Oct 3, 2024Oct 3, 2024
    • moalmanac

      Public
      Molecular Oncology Almanac, a clinical interpretation algorithm paired with a novel underlying knowledge base for precision cancer medicine
      HTML
      GNU General Public License v2.0
      41601Updated Oct 1, 2024Oct 1, 2024
    • Analysis of germline SVs in pediatric cancers
      Jupyter Notebook
      GNU General Public License v2.0
      0200Updated Sep 19, 2024Sep 19, 2024
    • comut

      Public
      CoMut is a Python library for visualizing genomic and phenotypic information via comutation plots
      Python
      MIT License
      2687104Updated Aug 1, 2024Aug 1, 2024
    • code and data for Liu, Schilling, et al Nat Med 2019
      Jupyter Notebook
      GNU General Public License v2.0
      61810Updated Aug 1, 2024Aug 1, 2024
    • Implementation repository for SigProfilerAssignment
      Python
      GNU General Public License v2.0
      0000Updated Jul 12, 2024Jul 12, 2024
    • Jupyter Notebook
      MIT License
      0000Updated May 30, 2024May 30, 2024
    • Terra storage helper
      Python
      GNU General Public License v2.0
      0042Updated May 21, 2024May 21, 2024
    • Web portal interface for browsing the Molecular Oncology Almanac
      Python
      GNU General Public License v2.0
      1112Updated Apr 11, 2024Apr 11, 2024
    • moalmanac-paper

      Public archive
      Analyses related to Reardon et al. 2021, Integrating molecular profiles into clinical frameworks through the Molecular Oncology Almanac to prospectively guide precision oncology
      HTML
      GNU General Public License v2.0
      4501Updated Mar 13, 2024Mar 13, 2024
    • pnet

      Public
      Implementation of P-Net as a flexible deep learning tool to generate insights from genetic features.
      Jupyter Notebook
      GNU General Public License v2.0
      4610Updated Feb 12, 2024Feb 12, 2024
    • Pilot exploration of overlap between germline and somatic alterations in common adult solid tumors
      R
      GNU General Public License v2.0
      0000Updated Feb 1, 2024Feb 1, 2024
    • Jupyter Notebook
      GNU General Public License v2.0
      0200Updated Jan 17, 2024Jan 17, 2024
    • A cloud-based web portal for accessible clinical interpretation of integrative cancer genomics.
      HTML
      GNU General Public License v2.0
      3135Updated Oct 3, 2023Oct 3, 2023
    • miniconda

      Public
      Dockerfiles for Miniconda
      Dockerfile
      GNU General Public License v2.0
      0300Updated Sep 14, 2023Sep 14, 2023
    • .github

      Public
      About the Van Allen lab at Dana-Farber Cancer Institute
      GNU General Public License v2.0
      0000Updated Sep 6, 2023Sep 6, 2023
    • beanie

      Public
      Tool for group biology estimation in single-cell RNAseq data
      Python
      GNU General Public License v2.0
      1500Updated Aug 16, 2023Aug 16, 2023
    • 2023-cgc

      Public
      Repository with notebook and slides for 2023 Cancer Genome Consortium workshop on the Molecular Oncology Almanac (moalmanac.org)
      HTML
      GNU General Public License v2.0
      0000Updated Aug 13, 2023Aug 13, 2023
    • Computational analysis of clinically actionable genomic features: Precision Heuristics for Interpreting the Alteration Landscape (PHIAL) - AACR 2017
      Jupyter Notebook
      GNU General Public License v2.0
      0100Updated Feb 16, 2023Feb 16, 2023
    • Cohort analysis of TCGA mc3 with PHIAL
      Jupyter Notebook
      GNU General Public License v2.0
      1200Updated Feb 16, 2023Feb 16, 2023
    • Algorithm for quantifying the number of translocation reads and wild-type reads in plasma samples with detectable ctDNA
      Shell
      GNU General Public License v2.0
      0000Updated Feb 16, 2023Feb 16, 2023
    • This workflow can be used to visualize the data from an *ABS_MAF.txt absolute file output. Both detection power and genomic locus are plotted for all SNPs, along with clustering information based on cancer cell fraction.
      Python
      GNU General Public License v2.0
      2100Updated Feb 16, 2023Feb 16, 2023
    • A class for calculating maf set intersections, with example scripts demonstrating usage.
      Python
      GNU General Public License v2.0
      0000Updated Feb 16, 2023Feb 16, 2023
    • Combine snv maf, indel maf, and titan allelic copy number calls, from either FACETS or TITAN, into the .tsv input PyClone requires.
      Python
      GNU General Public License v2.0
      6600Updated Feb 16, 2023Feb 16, 2023
    • This script takes in a tab-separated file containing at least one column of Ensembl IDs and a string indicating the header for this column, and outputs a tab-separated file identical to the input file except that it has an additional column containing mapped HGNC gene symbols for each row.
      Python
      GNU General Public License v2.0
      5200Updated Feb 16, 2023Feb 16, 2023
    • r2d2

      Public
      R2D2: RNA Normal/RNA Tumor, DNA Normal/DNA Tumor Analysis
      Jupyter Notebook
      GNU General Public License v2.0
      0100Updated Feb 16, 2023Feb 16, 2023
    • armbander

      Public
      A script that adds columns with arm and band-level information to any tab-separated file. Intended primarily for use with .seg-format files, but applicable across formats.
      Python
      GNU General Public License v2.0
      0000Updated Feb 16, 2023Feb 16, 2023
    • Python
      GNU General Public License v2.0
      0100Updated Feb 16, 2023Feb 16, 2023
    • FireCloud method: high-throughput visualization of splice junctions using ggsashimi package
      Python
      GNU General Public License v2.0
      0100Updated Feb 16, 2023Feb 16, 2023