Software

Genomic rearrangements

ToolDescriptionURL
GRIDSS2Genomic rearrangement callerhttps://github.com/PapenfussLab/gridss
GRIDSS1Genomic rearrangement callerhttps://github.com/PapenfussLab/gridss
VirusBreakEndVirus presence and genome integration detectionhttps://github.com/PapenfussLab/gridss
StructuralVariantAnnotationGeneric parser for SV VCFshttps://www.bioconductor.org/packages/release/bioc/html/StructuralVariantAnnotation.htm
CLOVESV classifierhttps://github.com/PapenfussLab/clove
SocratesFast & sensitive split read-based SV caller ttps://github.com/PapenfussLab/socrates


Genomic data analysis

KataegisBrowserKaetegis visualisationhttps://github.com/PapenfussLab/KataegisBrowser
Whole genome doubling testBranching process-based test for genome doublinghttps://github.com/PapenfussLab/Genome_doubling_test
HaveYouSwappedYourSampleSimple methods for detecting sample swapshttps://github.com/PapenfussLab/HaveYouSwappedYourSamples
CNspectorClinical copy number browserhttps://github.com/PapenfussLab/CNspector
CanarySNV callerhttps://github.com/PapenfussLab/Canary



Transcriptomic data analysis

TidyHeatmap
https://cran.r-project.org/web/packages/tidyHeatmap/index.html
TidySeurathttps://cran.r-project.org/web/packages/tidyseurat/index.html
TidyBulkhttps://bioconductor.org/packages/release/bioc/html/tidybulk.html
PPCseqhttps://github.com/stemangiola/ppcseq
assemble_varFramework for assembling Transcriptomics data (developed for P falciparum VAR genes)https://github.com/PapenfussLab/assemble_var


Pipeline frameworks

BioNixRobust framework for reproducible pipelines and software versioning based on the Nix build systemhttps://github.com/PapenfussLab/bionix
Bioshakehttps://github.com/PapenfussLab/bioshake

Deep Mutational Scanning

Enrich2https://github.com/FowlerLab/Enrich2

Clinical genomics

PathOSClinical informatics platformhttps://github.com/PapenfussLab/PathOS