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GIANA allows computationally-efficient TCR clustering and multi-disease repertoire classification by isometric transformation.
Zhang, Hongyi; Zhan, Xiaowei; Li, Bo.
  • Zhang H; Lyda Hill Department of Bioinformatics, UT Southwestern Medical Center, Dallas, TX, USA.
  • Zhan X; Department of Population and Data Science, UT Southwestern Medical Center, Dallas, TX, USA.
  • Li B; Lyda Hill Department of Bioinformatics, UT Southwestern Medical Center, Dallas, TX, USA. bo.li@utsouthwestern.edu.
Nat Commun ; 12(1): 4699, 2021 08 04.
Article in English | MEDLINE | ID: covidwho-1358351
ABSTRACT
Similarity in T-cell receptor (TCR) sequences implies shared antigen specificity between receptors, and could be used to discover novel therapeutic targets. However, existing methods that cluster T-cell receptor sequences by similarity are computationally inefficient, making them impractical to use on the ever-expanding datasets of the immune repertoire. Here, we developed GIANA (Geometric Isometry-based TCR AligNment Algorithm) a computationally efficient tool for this task that provides the same level of clustering specificity as TCRdist at 600 times its speed, and without sacrificing accuracy. GIANA also allows the rapid query of large reference cohorts within minutes. Using GIANA to cluster large-scale TCR datasets provides candidate disease-specific receptors, and provides a new solution to repertoire classification. Querying unseen TCR-seq samples against an existing reference differentiates samples from patients across various cohorts associated with cancer, infectious and autoimmune disease. Our results demonstrate how GIANA could be used as the basis for a TCR-based non-invasive multi-disease diagnostic platform.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Algorithms / Receptors, Antigen, T-Cell Type of study: Cohort study / Diagnostic study / Observational study / Prognostic study Limits: Humans Language: English Journal: Nat Commun Journal subject: Biology / Science Year: 2021 Document Type: Article Affiliation country: S41467-021-25006-7

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Algorithms / Receptors, Antigen, T-Cell Type of study: Cohort study / Diagnostic study / Observational study / Prognostic study Limits: Humans Language: English Journal: Nat Commun Journal subject: Biology / Science Year: 2021 Document Type: Article Affiliation country: S41467-021-25006-7