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MutationalPatterns
R package for extracting and visualizing mutational patterns in base substitution cataloguesRNASeq
RNASeq pipelineCHORD
An R package for predicting HR deficiency from mutation contextsNextflowModules
UMCU Genetics Nextflow modulesIAP
Illumina analysis pipelinePolarMorphism
Discovery of genetic variants with shared effect across multiple phenotypes from GWAS summary statisticsprimary-met-wgs-comparison
Code repo for all analysis done for the 'Pan-cancer whole genome comparison of primary and metastatic solid tumors' study.hpcguix-web
The code that drives https://hpc.guix.info/browse.COLO829_somaticSV
Scripts and files used in the generation of the COLO829 somatic SV truthset.mutSigExtractor
An R package for extracting mutational signatures from vcf filesvcf-explorer
Database and interface for vcf files.guix-additions
RNASeq-NF
RNASeq-NF is an NGS analysis pipeline for RNA expression quantification.sparqling-genomics
Ontologies, RDF-generators, and a web interface for querying it all.SHARC
DxNextflowWES
Genome Diagnostics Nextflow WES workflowexomedepth_scripts
scripts and tools for exomedepth based pipelineAdvancedBioinformaticsCourse
ExonCov
ExonCov: Exon coverage statistics from BAM filescuplr
Predicting tumor type using WGS derived featuresCWL-CommandLineTools
UMCU Genetics CWL CommandLineToolstumps
tumps: tumor purity simulationCWL
CWL workflowsDx_resources
Resources used in diagnostics pipelinesCyclomics_consensus_pipeline
Cyclomics consensus pipeline based on LAST and dagconGATK-QScripts
GATK QScripts used in our illumina variant calling pipeline.Complex_SVs
SNVFI
Genetic-Immune-Escape
Source code of the manuscript "Genetic immune escape landscape in primary and metastatic tumors"cwl-atacseq
cwl implementation of the ATAC-seq pipelineDx_tracks
pymc4c
A python based approach to processing MC4C databamMetrics
Tool to generate bam statistics and pdf/html reports.NF-IAP
Illumina Analysis Pipeline in Nextflowvcf-explorer_old
Vcf-explorer using couchDB - deprecatedGeoMx-DSP-analyses
Useq GeoMX DSP pipeline revisionDIMS
Direct Infusion Mass Spectrometry pipelineUSEQ_tools
Utility scripts to work with Genologics Clarity LIMSfingerprint_workflow
Comparison of workflow languages using the DX mip fingerprint pipeline.SmallTools
Small tools for genetics researchdIEM
For untargeted metabolomics, this tool calculates probability scores for metabolic disorders. In addition, it provides visual support with violin plots of the mass spectrometry (DI-HRMS) measurements for the lab specialists.mltoolkit
SyNet
Synergistic pair detectiongeneDriverAnnotator
CWL-IAP
CWL workflow implementation of IAP.RNASeq-CWL
CWL implementation of the UMCU/RNASeq pipelinePancreas_biobank
illumina-runinfo
Illumina runinfo web toolguix-workflows
Workflows for the GWLVirusSeq-CLI
CLI wrapper for the VirusSeq pipelineBachelorBfx
ipython notebooks for Bachelor course bioinformaticsFairDNA
Code from the DNA group developed during FAIR BYOD.MutationalPatterns-data
example data belonging to MutationalPatters packagetargetclone
TargetClone: A multi-sample approach for reconstructing subclonal evolution of tumorshmfGeneAnnotation
Determines the biallelic status of selected genes using SNV, indel and CNV datasmk-gwcyclomicsseq
snakemake pipeline for genome-wide cyclomics data processingVariantFiltering
clarity_epp
Clarity LIMS epp scriptsDxGenealogy
Genome Diagnostics Genealogymips
Scripts/tools for working with mip experiments.ONCODE_MC
Course materials for Oncode Masterclass: Introduction to machine learning in cancer genomics on the 18th November 2020 by Jeroen de Ridder's group (UMC Utrecht) in collaboration with Lodewyk Wessel and Soufiane Mourragui (NKI).CaddAnnotation
The CADD annotation pipeline annotates the contents of a tab-delimted database into an input VCF (in the INFO field). The chunkscript is used to run the annotation script in parallel, to annotate faster.Love Open Source and this site? Check out how you can help us