Evidence map›Paper›PMID 38109302›Full record

ArticleNucleic acids research2024

Language model-based B cell receptor sequence embeddings can effectively encode receptor specificity.

Meng Wang, Jonathan Patsenker, Henry Li, Yuval Kluger, Steven H Kleinstein

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
4.0field-weighted citation impact, top 6% of its field
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

16 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. AMULETY: A Python package to embed adaptive immune receptor sequences.Immunoinformatics (Amsterdam, Netherlands) · 2026
    Article
  6. Article
  7. Review
  8. Review
  9. Separating selection from mutation in antibody language models.bioRxiv : the preprint server for biology · 2025
    Article
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  11. Article
  12. Review
  13. Article
  14. Article
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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

5 authors at 1 institution in 1 country.

Meng WangProgram in Computational Biology and Bioinformatics, Yale University, New Haven, CT, USA.ORCID 0000-0002-3453-7805
Jonathan PatsenkerProgram in Applied Mathematics, Yale University, New Haven, CT, USA.
Henry LiProgram in Applied Mathematics, Yale University, New Haven, CT, USA.
Yuval KlugerProgram in Computational Biology and Bioinformatics, Yale University, New Haven, CT, USA.ORCID 0000-0002-3035-071X
Steven H KleinsteinProgram in Computational Biology and Bioinformatics, Yale University, New Haven, CT, USA.ORCID 0000-0003-4957-1544
Yale University · US

Funding

Yale SPORE in Skin CancerP50CA121974 · NCI · YALE UNIVERSITY · PI RUTH HALABAN · 2006 to 2026
$43.9M
COMPUTATIONAL TOOLS FOR THE ANALYSIS OF HIGH-THROUGHPUT IMMUNOGLOBULIN SEQUENCING EXPERIMENTSR01AI104739 · NIAID · YALE UNIVERSITY · PI KLEINSTEIN, STEVEN H. · 2014 to 2022
$3.6M
EFFICIENT METHODS FOR CALIBRATION, CLUSTERING, VISUALIZATION AND IMPUTATION OF LARGE scRNA-seq DATAR01GM131642 · NIGMS · YALE UNIVERSITY · PI KLUGER, YUVAL · 2019 to 2022
$1.6M
NCI NIH HHS P50 CA121974NIAID NIH HHS R01 AI104739NIGMS NIH HHS R01 GM131642
6 · The paper itself

Abstract

High throughput sequencing of B cell receptors (BCRs) is increasingly applied to study the immense diversity of antibodies. Learning biologically meaningful embeddings of BCR sequences is beneficial for predictive modeling. Several embedding methods have been developed for BCRs, but no direct performance benchmarking exists. Moreover, the impact of the input sequence length and paired-chain information on the prediction remains to be explored. We evaluated the performance of multiple embedding models to predict BCR sequence properties and receptor specificity. Despite the differences in model architectures, most embeddings effectively capture BCR sequence properties and specificity. BCR-specific embeddings slightly outperform general protein language models in predicting specificity. In addition, incorporating full-length heavy chains and paired light chain sequences improves the prediction performance of all embeddings. This study provides insights into the properties of BCR embeddings to improve downstream prediction applications for antibody analysis and discovery.

Indexed as

Natural Language ProcessingReceptors, Antigen, B-CellAmino Acid SequenceHigh-Throughput Nucleotide SequencingHumansImmunoglobulinsImmunoglobulinsReceptors, Antigen, B-Cell

Identifiers

PMID38109302
PMCPMC10810273
OpenAlexW4389924610

What OpenQuestion holds

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LicenceCC BY
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.