From: Tumor microenvironment: barrier or opportunity towards effective cancer therapy
Bioinformatics tools | Description | References |
---|---|---|
Identification of genome variant | ||
 GATK | Genome analysis toolkit Identify variants across genome using next generation sequencing data | [292] |
 MuTect | Somatic point mutation identification in cancer genomes | [291] |
HLA typing | ||
 Polysolver | Three major MHC I genes alleles identification based on whole exome sequencing data | [294] |
 OptiType | HLA genotyping algorithm that predicts all major and minor HLA class I alleles from next generation sequencing data | [293] |
MHC-binding affinity | ||
 netMHC/netMHCII/netMHCpan/netMHCpanII | Prediction of MHC binding affinity to Class I and Class II MHC molecules | |
 SMM | Sequence specificity-based quantitative model to identify binding affinity to MHC I molecules | [328] |
 SMMPMBEC | An amino acid similarity matrix derived based on experimental peptide-MHC binding interactions Act as Bayesian prior for prediction of peptide-MHC class I complex interaction | [329] |
 MHCflurry | Allele-specific neural networks trained on MHC ligands identified by mass spectrometry and binding affinity measurements to develop a model for prediction of MHC I complex proteins and their ligands | [330] |
 EDGE | Deep learning approach of HLA prediction based on training data from 74 patients | [301] |
Pipelines combining all steps of neoantigen prediction | ||
 FRED 2 | Prediction, selection, assembly and HLA typing of T-cell epitope | [302] |
 NetTepi | Predicts peptide-MHC (pMHC) binding affinity based on integration pMHC stability and T-cell propensity predictions | [304] |
 pVAC-Seq | Predicts tumor-specific neoantigen based on the integration of tumor mutation and expression data | [331] |