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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 databasebeanie
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 Carcinomamc_lightning_public
ped_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
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