2020plusClassifies genes as an oncogene, tumor suppressor gene, or as a non-driver gene by using Random Forests
MINTIEMethod for Identifying Novel Transcripts and Isoforms using Equivalence classes, in cancer and rare disease.
Front-EndFederated Learning based Deep Learning. Docs: https://fets-ai.github.io/Front-End/
RNAseq titration resultsCross-platform normalization enables machine learning model training on microarray and RNA-seq data simultaneously
civic-clientWeb client for CIViC: Clinical Interpretations of Variants in Cancer
OmiEmbedMulti-task deep learning framework for multi-omics data analysis
smartas📓Notebook of Climente-González et al. (2017), The Functional Impact of Alternative Splicing in Cancer.
shiny-iatlasAn interactive web portal for exploring immuno-oncology data
hotspot3d3D hotspot mutation proximity analysis tool
civicmineText mining cancer biomarkers for the CIVIC database
IARC-nfList of IARC bioinformatics nextflow pipelines
cpsrCancer Predisposition Sequencing Reporter (CPSR)
GeneFuseGene fusion detection and visualization
cancer-dataTCGA data acquisition and processing for Project Cognoma
arribaFast and accurate gene fusion detection from RNA-Seq data
ci4cc-informatics-resourcesCommunity-maintained list of resources that the CI4CC organization and the larger cancer informatics community have found useful or are developing.
mageriMAGERI - Assemble, align and call variants for targeted genome re-sequencing with unique molecular identifiers
cacaoCallable Cancer Loci - assessment of sequencing coverage for actionable and pathogenic loci in cancer