Evidence map›Paper›PMID 36451811›Full record

ArticleFrontiers in immunology2022

pyTCR: A comprehensive and scalable solution for TCR-Seq data analysis to facilitate reproducibility and rigor of immunogenomics research.

Kerui Peng, Jaden Moore, Mohammad Vahed, Jaqueline Brito, Guoyun Kao, Amanda M Burkhardt, Houda Alachkar, Serghei Mangul

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 44% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. 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

8 authors at 1 institution in 1 country.

Kerui PengDepartment of Clinical Pharmacy, School of Pharmacy, University of Southern California, Los Angeles, CA, United States.
Jaden MooreDepartment of Clinical Pharmacy, School of Pharmacy, University of Southern California, Los Angeles, CA, United States.
Mohammad VahedDepartment of Clinical Pharmacy, School of Pharmacy, University of Southern California, Los Angeles, CA, United States.
Jaqueline BritoDepartment of Clinical Pharmacy, School of Pharmacy, University of Southern California, Los Angeles, CA, United States.
Guoyun KaoDepartment of Pharmacology and Pharmaceutical Sciences, School of Pharmacy, University of Southern California, Los Angeles, CA, United States.
Amanda M BurkhardtDepartment of Clinical Pharmacy, School of Pharmacy, University of Southern California, Los Angeles, CA, United States.
Houda AlachkarDepartment of Clinical Pharmacy, School of Pharmacy, University of Southern California, Los Angeles, CA, United States.
Serghei MangulDepartment of Clinical Pharmacy, School of Pharmacy, University of Southern California, Los Angeles, CA, United States.
University of Southern California · US

Funding

Mentored Career DevelopmentKL2TR001854 · NCATS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Elizabeth Rhea Erwin Burner, Amy Elizabeth West · 2016 to 2026
$9.0M
Leveraging the TCR Repertoire to identify target neoantigens in FLT3-ITD positive Acute Myeloid LeukemiaR01CA248381 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI ALACHKAR, HOUDA · 2021 to 2025
$1.8M
NCATS NIH HHS KL2 TR001854NCI NIH HHS R01 CA248381
6 · The paper itself

Abstract

T cell receptor (TCR) studies have grown substantially with the advancement in the sequencing techniques of T cell receptor repertoire sequencing (TCR-Seq). The analysis of the TCR-Seq data requires computational skills to run the computational analysis of TCR repertoire tools. However biomedical researchers with limited computational backgrounds face numerous obstacles to properly and efficiently utilizing bioinformatics tools for analyzing TCR-Seq data. Here we report pyTCR, a computational notebook-based solution for comprehensive and scalable TCR-Seq data analysis. Computational notebooks, which combine code, calculations, and visualization, are able to provide users with a high level of flexibility and transparency for the analysis. Additionally, computational notebooks are demonstrated to be user-friendly and suitable for researchers with limited computational skills. Our tool has a rich set of functionalities including various TCR metrics, statistical analysis, and customizable visualizations. The application of pyTCR on large and diverse TCR-Seq datasets will enable the effective analysis of large-scale TCR-Seq data with flexibility, and eventually facilitate new discoveries.

Indexed as

Data AnalysisReceptors, Antigen, T-CellComputational BiologyReproducibility of ResultsReceptors, Antigen, T-Cellcomputational notebooksimmunogenomicsreproducibilityTCR characterizationTCR-seqTCR - T cell receptor

Identifiers

PMID36451811
PMCPMC9704496
OpenAlexW4307635541

What OpenQuestion holds

Textmetadata
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.