Evidence map›Paper›PMID 37293077›Full record

ArticlebioRxiv : the preprint server for biology2023

Neural Network Models for Sequence-Based TCR and HLA Association Prediction.

Si Liu, Philip Bradley, Wei Sun

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed, 4 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

Si LiuPublic Health Science Division, Fred Hutchinson Cancer Center, Seattle, USA.
Philip BradleyPublic Health Science Division, Fred Hutchinson Cancer Center, Seattle, USA.
Wei SunPublic Health Science Division, Fred Hutchinson Cancer Center, Seattle, USA.
Fred Hutch Cancer Center · USUniversity of North Carolina at Chapel Hill · US

Funding

Statistical Methods for T Cell Receptor (TCR) AnalysisR56AI169192 · NIAID · FRED HUTCHINSON CANCER CENTER · PI SUN, WEI · 2022 to 2022
$330k
NIAID NIH HHS R56 AI169192
6 · The paper itself

Abstract

T cells rely on their T cell receptors (TCRs) to recognize foreign antigens presented by human leukocyte antigen (HLA) proteins. TCRs contain a record of an individual's past immune activities, and some TCRs are observed only in individuals with certain HLA alleles. As a result, characterising TCRs requires a thorough understanding of TCR-HLA associations. To this end, we propose a neural network method named Deep learning Prediction of TCR-HLA association (DePTH) to predict TCR-HLA associations based on their amino acid sequences. We show that the DePTH can be used to quantify the functional similarities of HLA alleles, and that these HLA similarities are associated with the survival outcomes of cancer patients who received immune checkpoint blockade treatment.

Indexed as

amino acid sequencehuman leukocyte antigenimmune checkpoint blockadeneural networkT cell receptor

Identifiers

PMID37293077
PMCPMC10245990
OpenAlexW4378363596

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.