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OLGA: fast computation of generation probabilities of B- and T-cell receptor amino acid sequences and motifs

Author(s): Sethna, Zachary; Elhanati, Yuval; Callan Jr, Curtis G; Walczak, Aleksandra M; Mora, Thierry

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Abstract: Motivation: High-throughput sequencing of large immune repertoires has enabled the development of methods to predict the probability of generation by V(D)J recombination of T- and B-cell receptors of any specific nucleotide sequence. These generation probabilities are very non-homogeneous, ranging over 20 orders of magnitude in real repertoires. Since the function of a receptor really depends on its protein sequence, it is important to be able to predict this probability of generation at the amino acid level. However, brute-force summation over all the nucleotide sequences with the correct amino acid translation is computationally intractable. The purpose of this paper is to present a solution to this problem. Results: We use dynamic programming to construct an efficient and flexible algorithm, called OLGA (Optimized Likelihood estimate of immunoGlobulin Amino-acid sequences), for calculating the probability of generating a given CDR3 amino acid sequence or motif, with or without V/J restriction, as a result of V(D)J recombination in B or T cells. We apply it to databases of epitope-specific T-cell receptors to evaluate the probability that a typical human subject will possess T cells responsive to specific disease-associated epitopes. The model prediction shows an excellent agreement with published data. We suggest that OLGA may be a useful tool to guide vaccine design.
Publication Date: 1-Sep-2019
Citation: Sethna, Zachary, Elhanati, Yuval, Callan, Curtis G, Walczak, Aleksandra M, Mora, Thierry. (2019). OLGA: fast computation of generation probabilities of B- and T-cell receptor amino acid sequences and motifs. BIOINFORMATICS, 35 (2974 - 2981. doi:10.1093/bioinformatics/btz035
DOI: doi:10.1093/bioinformatics/btz035
ISSN: 1367-4803
EISSN: 1460-2059
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Pages: 2974 - 2981
Type of Material: Journal Article
Journal/Proceeding Title: BIOINFORMATICS
Version: Final published version. Article is made available in OAR by the publisher's permission or policy.

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