Van Allen Lab (@vanallenlab)

Top repositories

1

comut

CoMut is a Python library for visualizing genomic and phenotypic information via comutation plots
Python
87
star
2

retained-intron-neoantigen-pipeline

Pipeline to call neoantigens from intron retention events derived from RNA-Seq data.
Python
28
star
3

schadendorf-pd1

code and data for Liu, Schilling, et al Nat Med 2019
Jupyter Notebook
18
star
4

moalmanac

Molecular Oncology Almanac, a clinical interpretation algorithm paired with a novel underlying knowledge base for precision cancer medicine
HTML
16
star
5

MutPanningV2

This repository contains the source code of the revised version of MutPanning. MutPanning is publicly available under the BSD3-Clause open source license.
Java
12
star
6

neoantigen_calling_pipeline

Pipeline to call somatic cancer neoantigens from mutations in patient tumor DNA
Python
12
star
7

facets

Implementation of FACETS for Terra
WDL
11
star
8

PyCloneTSVGeneration_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.
Python
6
star
9

moalmanac-db

Underlying content for the Molecular Oncology Almanac's database
5
star
10

moalmanac-paper

Analyses related to Reardon et al. 2021, Integrating molecular profiles into clinical frameworks through the Molecular Oncology Almanac to prospectively guide precision oncology
HTML
5
star
11

beanie

Tool for group biology estimation in single-cell RNAseq data
Python
5
star
12

VanAllen_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.
5
star
13

phial

Precision Heuristics for Interpreting the Alteration Landscape
R
4
star
14

pnet

Implementation of P-Net as a flexible deep learning tool to generate insights from genetic features.
Jupyter Notebook
4
star
15

deconstruct_sigs_py

DeconstructSigs algorithm in python.
Python
3
star
16

common_variant_filter

A simple filter to annotate and filter somatic or germline variants based on their observed allele counts in ExAC
Python
3
star
17

2017-tcga-mc3_phial

Cohort analysis of TCGA mc3 with PHIAL
Jupyter Notebook
2
star
18

OncoPathwayDraw

Jupyter Notebook
2
star
19

microhet-paper

Jupyter Notebook
2
star
20

2016-Mouw_ASCC

Mouw et. al 2016, Genomic Evolution After Chemoradiotherapy in Anal Squamous Cell Carcinoma
Jupyter Notebook
2
star
21

mc_lightning_public

Python
2
star
22

ped_germline_SV

Analysis of germline SVs in pediatric cancers
Jupyter Notebook
2
star
23

EnsemblToHGNC

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
2
star
24

automated_DbGaP_DataRetrieval

FireCloud method that Retrieves DbGaP SRA files and converts them to BAM files
Dockerfile
1
star
25

mpcproject-paper

A repository that contains code and data used to generate the figures for the MPCproject manuscript
Jupyter Notebook
1
star
26

VALab_Bi_He_ccRCC_scRNASeq_2021

HTML
1
star
27

r2d2

R2D2: RNA Normal/RNA Tumor, DNA Normal/DNA Tumor Analysis
Jupyter Notebook
1
star
28

mapq_plotter

Python
1
star
29

single_cell_help

Vignettes and scripts for pre-processing and analysis of single-cell and single-nuclei RNA-Seq data
Jupyter Notebook
1
star
30

training_with_abstention

Code supporting manuscript doi: https://doi.org/10.1101/2021.09.14.460365
Jupyter Notebook
1
star
31

SpliceJunctionVisualization

FireCloud method: high-throughput visualization of splice junctions using ggsashimi package
Python
1
star
32

moalmanac-portal

A cloud-based web portal for accessible clinical interpretation of integrative cancer genomics.
HTML
1
star
33

moalmanac-browser

Web portal interface for browsing the Molecular Oncology Almanac
Python
1
star
34

abs_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.
Python
1
star
35

2017-aacr_phial2

Computational analysis of clinically actionable genomic features: Precision Heuristics for Interpreting the Alteration Landscape (PHIAL) - AACR 2017
Jupyter Notebook
1
star
36

miniconda

Dockerfiles for Miniconda
Dockerfile
1
star