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pyensembl
Python interface to access reference genome features (such as genes, transcripts, and exons) from Ensemblmhcflurry
Peptide-MHC I binding affinity predictiongtfparse
Parsing tools for GTF (gene transfer format) filesmhctools
Python interface to running command-line and web-based MHC binding predictorsvarcode
Library for manipulating genomic variants and predicting their effectsneoantigen-vaccine-pipeline
Bioinformatics pipeline for selecting patient-specific cancer neoantigen vaccinesvaxrank
Ranked vaccine peptides for personalized cancer immunotherapypepdata
Python interface to amino acid properties and IEDBtopiary
Predict mutated T-cell epitopes from sequencing dataisovar
Assembly of RNA reads to determine the effect of a cancer mutation on protein sequencepepnet
Neural networks for amino acid sequencesvarlens
commandline manipulation of genomic variants and NGS readsgene-lists
Gene lists related to cancer immunotherapytcga-immune-deconvolution
Immune deconvolution of publicly available TCGA expression datamhcnames
All the fun and adventure of MHC naming, now in Pythondatacache
Helpers for transparently downloading datasetscancer-cell-line-mhc-alleles
Cell line HLA types and neoepitope catalog from TCLPmhcdouble
Class II MHC binding and antigen processing predictionott-wu-2017-data
Machine readable data from "An Immunogenic Personal Neoantigen Vaccine for Melanoma Patients"mhc2-data
Class II MHC datasahin-2017-data
Machine readable data from "Personalized RNA mutanome vaccines mobilize poly-specific therapeutic immunity against cancer"vaxrank-paper-2018
Repository for updated Vaxrank paperproteopt
Common interface to protein design tools and structure predictorsmhcflurry-motifs
Motifs for MHC I alleles as predicted by MHCflurrymhc2flurry
MHC class II binding predictor, under developmentcov-2-mutations-by-lineage
Quick analysis to associate SARS-Cov-2 spike mutations with pangolin lineages using GISAID dataLove Open Source and this site? Check out how you can help us