ArticleBioinformatics (Oxford, England)2016
repgenHMM: a dynamic programming tool to infer the rules of immune receptor generation from sequence data.
Article in Bioinformatics (Oxford, England), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.
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Who cites it
23 citing papers in PubMed.
- Thymic function as a central determinant of immune competence and clinical outcomes.Seminars in immunopathology · 2026Review
- Benchmarking data-driven filtering for denoising of TCRpMHC single-cell data.Scientific reports · 2023Article
- Antibody repertoire sequencing analysis.Acta biochimica et biophysica Sinica · 2022Review
- A framework for highly multiplexed dextramer mapping and prediction of T cell receptor sequences to antigen specificity.Science advances · 2021Article
- Dynamics of thymus function and T cell receptor repertoire breadth in health and disease.Seminars in immunopathology · 2021Review
- Using the T Cell Receptor as a Biomarker in Type 1 Diabetes.Frontiers in immunology · 2021Review
- How repertoire data are changing antibody science.The Journal of biological chemistry · 2020Review
- Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.Nature genetics · 2020Article
- OLGA: fast computation of generation probabilities of B- and T-cell receptor amino acid sequences and motifs.Bioinformatics (Oxford, England) · 2019Article
- Genesis of the αβ T-cell receptor.PLoS computational biology · 2019Article
- The expanding role of systems immunology in decoding the T cell receptor repertoire.Current opinion in systems biology · 2018Article
- High-throughput sequencing of the T-cell receptor repertoire: pitfalls and opportunities.Briefings in bioinformatics · 2018Article
- The Bayesian optimist's guide to adaptive immune receptor repertoire analysis.Immunological reviews · 2018Review
- Predicting the spectrum of TCR repertoire sharing with a data-driven model of recombination.Immunological reviews · 2018Review
- High-throughput immune repertoire analysis with IGoR.Nature communications · 2018Article
- Comparative analysis of murine T-cell receptor repertoires.Immunology · 2018Review
- Network Representation of T-Cell Repertoire- A Novel Tool to Analyze Immune Response to Cancer Formation.Frontiers in immunology · 2018Article
- Computational Strategies for Dissecting the High-Dimensional Complexity of Adaptive Immune Repertoires.Frontiers in immunology · 2018Review
- Analyzing Immunoglobulin Repertoires.Frontiers in immunology · 2018Review
- Persisting fetal clonotypes influence the structure and overlap of adult human T cell receptor repertoires.PLoS computational biology · 2017Article
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4 authors.
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No grant is acknowledged in the PubMed record.
Abstract
motivationThe diversity of the immune repertoire is initially generated by random rearrangements of the receptor gene during early T and B cell development. Rearrangement scenarios are composed of random events-choices of gene templates, base pair deletions and insertions-described by probability distributions. Not all scenarios are equally likely, and the same receptor sequence may be obtained in several different ways. Quantifying the distribution of these rearrangements is an essential baseline for studying the immune system diversity. Inferring the properties of the distributions from receptor sequences is a computationally hard problem, requiring enumerating every possible scenario for every sampled receptor sequence.
resultsWe present a Hidden Markov model, which accounts for all plausible scenarios that can generate the receptor sequences. We developed and implemented a method based on the Baum-Welch algorithm that can efficiently infer the parameters for the different events of the rearrangement process. We tested our software tool on sequence data for both the alpha and beta chains of the T cell receptor. To test the validity of our algorithm, we also generated synthetic sequences produced by a known model, and confirmed that its parameters could be accurately inferred back from the sequences. The inferred model can be used to generate synthetic sequences, to calculate the probability of generation of any receptor sequence, as well as the theoretical diversity of the repertoire. We estimate this diversity to be [Formula: see text] for human T cells. The model gives a baseline to investigate the selection and dynamics of immune repertoires. AVAILABILITY AND IMPLEMENTATION: Source code and sample sequence files are available at https://bitbucket.org/yuvalel/repgenhmm/downloads CONTACT: elhanati@lpt.ens.fr or tmora@lps.ens.fr or awalczak@lpt.ens.fr.
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