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comut
CoMut is a Python library for visualizing genomic and phenotypic information via comutation plotsretained-intron-neoantigen-pipeline
Pipeline to call neoantigens from intron retention events derived from RNA-Seq data.schadendorf-pd1
code and data for Liu, Schilling, et al Nat Med 2019moalmanac
Molecular Oncology Almanac, a clinical interpretation algorithm paired with a novel underlying knowledge base for precision cancer medicineMutPanningV2
This repository contains the source code of the revised version of MutPanning. MutPanning is publicly available under the BSD3-Clause open source license.neoantigen_calling_pipeline
Pipeline to call somatic cancer neoantigens from mutations in patient tumor DNAfacets
Implementation of FACETS for TerraPyCloneTSVGeneration_FACETS_or_TITAN
Combine snv maf, indel maf, and titan allelic copy number calls, from either FACETS or TITAN, into the .tsv input PyClone requires.moalmanac-db
Underlying content for the Molecular Oncology Almanac's databasemoalmanac-paper
Analyses related to Reardon et al. 2021, Integrating molecular profiles into clinical frameworks through the Molecular Oncology Almanac to prospectively guide precision oncologybeanie
Tool for group biology estimation in single-cell RNAseq dataVanAllen_CTLA4_Science_RNASeq_TPM
Contains TPM matrix (produced by RSEM) for pre-treatment samples from N = 42 ipilimumab-treated melanoma patients published in Van Allen et al. Science 2015.phial
Precision Heuristics for Interpreting the Alteration Landscapepnet
Implementation of P-Net as a flexible deep learning tool to generate insights from genetic features.deconstruct_sigs_py
DeconstructSigs algorithm in python.common_variant_filter
A simple filter to annotate and filter somatic or germline variants based on their observed allele counts in ExAC2017-tcga-mc3_phial
Cohort analysis of TCGA mc3 with PHIALOncoPathwayDraw
microhet-paper
2016-Mouw_ASCC
Mouw et. al 2016, Genomic Evolution After Chemoradiotherapy in Anal Squamous Cell Carcinomaped_germline_SV
Analysis of germline SVs in pediatric cancersEnsemblToHGNC
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.automated_DbGaP_DataRetrieval
FireCloud method that Retrieves DbGaP SRA files and converts them to BAM filesmpcproject-paper
A repository that contains code and data used to generate the figures for the MPCproject manuscriptVALab_Bi_He_ccRCC_scRNASeq_2021
r2d2
R2D2: RNA Normal/RNA Tumor, DNA Normal/DNA Tumor Analysismapq_plotter
single_cell_help
Vignettes and scripts for pre-processing and analysis of single-cell and single-nuclei RNA-Seq datatraining_with_abstention
Code supporting manuscript doi: https://doi.org/10.1101/2021.09.14.460365SpliceJunctionVisualization
FireCloud method: high-throughput visualization of splice junctions using ggsashimi packagemoalmanac-portal
A cloud-based web portal for accessible clinical interpretation of integrative cancer genomics.moalmanac-browser
Web portal interface for browsing the Molecular Oncology Almanacabs_maf_clustering_vis
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.2017-aacr_phial2
Computational analysis of clinically actionable genomic features: Precision Heuristics for Interpreting the Alteration Landscape (PHIAL) - AACR 2017miniconda
Dockerfiles for MinicondaLove Open Source and this site? Check out how you can help us