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- W1991036680 endingPage "S3" @default.
- W1991036680 startingPage "S3" @default.
- W1991036680 abstract "Sequence based T-cell epitope predictions have improved immensely in the last decade. From predictions of peptide binding to major histocompatibility complex molecules with moderate accuracy, limited allele coverage, and no good estimates of the other events in the antigen-processing pathway, the field has evolved significantly. Methods have now been developed that produce highly accurate binding predictions for many alleles and integrate both proteasomal cleavage and transport events. Moreover have so-called pan-specific methods been developed, which allow for prediction of peptide binding to MHC alleles characterized by limited or no peptide binding data. Most of the developed methods are publicly available, and have proven to be very useful as a shortcut in epitope discovery. Here, we will go through some of the history of sequence-based predictions of helper as well as cytotoxic T cell epitopes. We will focus on some of the most accurate methods and their basic background." @default.
- W1991036680 created "2016-06-24" @default.
- W1991036680 creator A5004763412 @default.
- W1991036680 creator A5068661538 @default.
- W1991036680 creator A5071462078 @default.
- W1991036680 creator A5076702280 @default.
- W1991036680 date "2010-01-01" @default.
- W1991036680 modified "2023-09-25" @default.
- W1991036680 title "State of the art and challenges in sequence based T-cell epitope prediction" @default.
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