Abstract

BackgroundCancer neoantigens have attracted great interest in immunotherapy due to their capacity to elicit antitumoral responses. These molecules arise from somatic mutations in cancer cells, resulting in alterations on the original protein. Neoantigens identification remains a challenging task due largely to a high rate of false-positives.ResultsWe have developed an efficient and automated pipeline for the identification of potential neoantigens. neoANT-HILL integrates several immunogenomic analyses to improve neoantigen detection from Next Generation Sequence (NGS) data. The pipeline has been compiled in a pre-built Docker image such that minimal computational background is required for download and setup. NeoANT-HILL was applied in The Cancer Genome Atlas (TCGA) melanoma dataset and found several putative neoantigens including ones derived from the recurrent RAC1:P29S and SERPINB3:E250K mutations. neoANT-HILL was also used to identify potential neoantigens in RNA-Seq data with a high sensitivity and specificity.ConclusionneoANT-HILL is a user-friendly tool with a graphical interface that performs neoantigens prediction efficiently. neoANT-HILL is able to process multiple samples, provides several binding predictors, enables quantification of tumor-infiltrating immune cells and considers RNA-Seq data for identifying potential neoantigens. The software is available through github at https://github.com/neoanthill/neoANT-HILL.

Highlights

  • Cancer neoantigens have attracted great interest in immunotherapy due to their capacity to elicit antitumoral responses

  • Recent studies have demonstrated that T cells can recognize tumor-specific antigens that bind to human leukocyte antigens (HLA) molecules at the surface of tumor cells [1, 2]

  • We present a versatile tool with a graphical user interface (GUI), called neoANT-HILL, designed to identify potential neoantigens arising from cancer somatic mutations. neoANT-HILL integrates complementary features to prioritizing mutant peptides based on predicted binding affinity and mRNA expression level (Fig. 1)

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Summary

Introduction

Cancer neoantigens have attracted great interest in immunotherapy due to their capacity to elicit antitumoral responses. None of these proposed tools considers tumor transcriptome sequencing data (RNA-seq) for identifying somatic mutations. We present a versatile tool with a graphical user interface (GUI), called neoANT-HILL, designed to identify potential neoantigens arising from cancer somatic mutations. RNA sequencing project [12] to demonstrate that RNA-seq is a potential source of mutation detection.

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