Evidence map›Paper›PMID 32802272›Full record

ReviewComputational and structural biotechnology journal2020

Methods for sequence and structural analysis of B and T cell receptor repertoires.

Shunsuke Teraguchi, Dianita S Saputri, Mara Anais Llamas-Covarrubias, Ana Davila, Diego Diez, Sedat Aybars Nazlica, John Rozewicki, Hendra S Ismanto, Jan Wilamowski, Jiaqi Xie and 5 more

Abstract readReview
In one paragraph

Review in Computational and structural biotechnology journal, 2020. 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.

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  17. Advances in Lymphoma Molecular Diagnostics.Diagnostics (Basel, Switzerland) · 2021
    Review
  18. Article
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  20. Progress toward improved understanding of antibody maturation.Current opinion in structural biology · 2021
    Review
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

15 authors.

Shunsuke TeraguchiImmunology Frontier Research Center, Osaka University, 3-1 Yamadaoka, Suita, Japan.
Dianita S SaputriResearch Institute for Microbial Diseases, Osaka University, 3-1 Yamadaoka, Suita, Japan.
Mara Anais Llamas-CovarrubiasResearch Institute for Microbial Diseases, Osaka University, 3-1 Yamadaoka, Suita, Japan.
Ana DavilaResearch Institute for Microbial Diseases, Osaka University, 3-1 Yamadaoka, Suita, Japan.
Diego DiezImmunology Frontier Research Center, Osaka University, 3-1 Yamadaoka, Suita, Japan.
Sedat Aybars NazlicaImmunology Frontier Research Center, Osaka University, 3-1 Yamadaoka, Suita, Japan.
John RozewickiImmunology Frontier Research Center, Osaka University, 3-1 Yamadaoka, Suita, Japan.
Hendra S IsmantoResearch Institute for Microbial Diseases, Osaka University, 3-1 Yamadaoka, Suita, Japan.
Jan WilamowskiResearch Institute for Microbial Diseases, Osaka University, 3-1 Yamadaoka, Suita, Japan.
Jiaqi XieResearch Institute for Microbial Diseases, Osaka University, 3-1 Yamadaoka, Suita, Japan.
Zichang XuResearch Institute for Microbial Diseases, Osaka University, 3-1 Yamadaoka, Suita, Japan.
Martin de Jesus Loza-LopezImmunology Frontier Research Center, Osaka University, 3-1 Yamadaoka, Suita, Japan.
Floris J van EerdenImmunology Frontier Research Center, Osaka University, 3-1 Yamadaoka, Suita, Japan.
Songling LiResearch Institute for Microbial Diseases, Osaka University, 3-1 Yamadaoka, Suita, Japan.
Daron M StandleyImmunology Frontier Research Center, Osaka University, 3-1 Yamadaoka, Suita, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

B cell receptors (BCRs) and T cell receptors (TCRs) make up an essential network of defense molecules that, collectively, can distinguish self from non-self and facilitate destruction of antigen-bearing cells such as pathogens or tumors. The analysis of BCR and TCR repertoires plays an important role in both basic immunology as well as in biotechnology. Because the repertoires are highly diverse, specialized software methods are needed to extract meaningful information from BCR and TCR sequence data. Here, we review recent developments in bioinformatics tools for analysis of BCR and TCR repertoires, with an emphasis on those that incorporate structural features. After describing the recent sequencing technologies for immune receptor repertoires, we survey structural modeling methods for BCR and TCRs, along with methods for clustering such models. We review downstream analyses, including BCR and TCR epitope prediction, antibody-antigen docking and TCR-peptide-MHC Modeling. We also briefly discuss molecular dynamics in this context.

Indexed as

Adaptive immunologyAntigenB cell receptorClusteringImmune systemMachine-learningSingle cell sequencingT cell receptor

Identifiers

PMID32802272
PMCPMC7366105

What OpenQuestion holds

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Registered trials

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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.