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phylowgs
Application for inferring subclonal composition and evolution from whole-genome sequencing data.TrackSig
A framework to infer mutational signatures in cancer over timeqapa
RNA-seq Quantification of Alternative Polyadenylationpairtree
Pairtree is a method for reconstructing cancer evolutionary history in individual patients, and analyzing intratumor genetic heterogeneity. Pairtree focuses on scaling to many more cancer samples and cancer cell subpopulations than other algorithms, and on producing concise and informative interactive characterizations of posterior uncertainty.mlworkshop
Machine learning workshop presented at GLBIO 2016phylosub
submarine
Code for SubMARine.RNAcompete
Data analysis scripts for RNAcompete.rnascan
Python package for scanning RNA sequences with sequence and structure PFMsTrackSigFreq
R package for TrackSig and TrackSigFreqorchard
GenomeTrackSig
damuta
Tandem signatures of DNA damage and misrepair in cancersmchet-challenge
Data related to the ICGC-TCGA DREAM Somatic Mutation Calling - Tumour Heterogeneity Challenge.consensus-bp
Pipeline for creating consensus copy-number aberration (CNA) segmentation (breakpoints) for ICGC Pan Cancer Analysis of Whole Genomes project. Used in paper at https://www.biorxiv.org/content/10.1101/312041v5.submarine_data
Simulated data SubMARine was evaluated on.plos-medicine-joint-patterns
Source code for the juvenile idiopathic arthritis joint patterns paper published in PLOS Medicine, 2019.PAN-cODE
RNAcompete_classifier
This repository contains the code and data for training the RNAcompete experiment classifier used in Ray et al. 2022weme
Weighted Median subclonal consensus methodLove Open Source and this site? Check out how you can help us