Evidence map›Paper›PMID 27153709›Full record

ArticleBioinformatics (Oxford, England)2016

repgenHMM: a dynamic programming tool to infer the rules of immune receptor generation from sequence data.

Yuval Elhanati, Quentin Marcou, Thierry Mora, Aleksandra M Walczak

Abstract read
In one paragraph

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.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

23 citing papers in PubMed.

  1. Review
  2. Article
  3. Antibody repertoire sequencing analysis.Acta biochimica et biophysica Sinica · 2022
    Review
  4. Article
  5. Review
  6. Review
  7. How repertoire data are changing antibody science.The Journal of biological chemistry · 2020
    Review
  8. Article
  9. Article
  10. Genesis of the αβ T-cell receptor.PLoS computational biology · 2019
    Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Review
  17. Article
  18. Review
  19. Analyzing Immunoglobulin Repertoires.Frontiers in immunology · 2018
    Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Yuval ElhanatiLaboratoire de physique théorique, CNRS, UPMC and Ecole normale supérieure, Paris, France.
Quentin MarcouLaboratoire de physique théorique, CNRS, UPMC and Ecole normale supérieure, Paris, France.
Thierry MoraLaboratoire de physique statistique, CNRS, UPMC and Ecole normale supérieure, Paris, France.
Aleksandra M WalczakLaboratoire de physique théorique, CNRS, UPMC and Ecole normale supérieure, Paris, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Gene Rearrangement, T-LymphocyteSoftwareV(D)J RecombinationAlgorithmsHumansProbabilityReceptors, Antigen, T-CellSequence AlignmentReceptors, Antigen, T-Cell

Identifiers

PMID27153709
PMCPMC4920122

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.