Tao Yue,Si-Yi Chen,Wen-Kang Shen,Yu Liao,Qian Lei,An-Yuan Guo
{"title":"TCRdb 2.0: an updated T-cell receptor sequence database.","authors":"Tao Yue,Si-Yi Chen,Wen-Kang Shen,Yu Liao,Qian Lei,An-Yuan Guo","doi":"10.1093/nar/gkaf876","DOIUrl":null,"url":null,"abstract":"T-cell receptor (TCR) repertoire sequencing allows researchers to analyze millions of TCRs, providing unparalleled precision in understanding immune responses and enabling broad applications. However, existing TCR-related databases are based on a limited number of samples. Here, we present TCRdb2.0 (https://guolab.wchscu.cn/TCRdb2/#/), an updated and significantly expanded resource with enriched data and enhanced functionalities. TCRdb2.0 incorporates ∼700 million TCR sequences derived from 19 701 TCR-Seq samples across 46 tissues and 147 clinical conditions, making it the most comprehensive TCR sequence database to date. The homepage of TCRdb2.0 has powerful browsing, searching and downloading functions. It displays multiple features of TCR in sample and project levels. Compared to the previous release, TCRdb2.0 has the following major improvements: (i) a substantial increase of TCR sequences, from 277 million to ∼700 million; (ii) inclusion of TCR sequences from Gamma delta (γδ) T cells; (iii) integration of therapy-related TCR-Seq datasets, such as programmed cell death 1 (PD-1) blockade immunotherapy; (iv) construction of the largest TCR sequence reference from healthy samples; and (v) redesign of a new search and download function, enabling flexible queries and downloads. With its extensive data and user-friendly web interface, TCRdb2.0 will serve as an invaluable resource for functional studies of TCRs in both health and disease.","PeriodicalId":19471,"journal":{"name":"Nucleic Acids Research","volume":"17 1","pages":""},"PeriodicalIF":13.1000,"publicationDate":"2025-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nucleic Acids Research","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/nar/gkaf876","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
T-cell receptor (TCR) repertoire sequencing allows researchers to analyze millions of TCRs, providing unparalleled precision in understanding immune responses and enabling broad applications. However, existing TCR-related databases are based on a limited number of samples. Here, we present TCRdb2.0 (https://guolab.wchscu.cn/TCRdb2/#/), an updated and significantly expanded resource with enriched data and enhanced functionalities. TCRdb2.0 incorporates ∼700 million TCR sequences derived from 19 701 TCR-Seq samples across 46 tissues and 147 clinical conditions, making it the most comprehensive TCR sequence database to date. The homepage of TCRdb2.0 has powerful browsing, searching and downloading functions. It displays multiple features of TCR in sample and project levels. Compared to the previous release, TCRdb2.0 has the following major improvements: (i) a substantial increase of TCR sequences, from 277 million to ∼700 million; (ii) inclusion of TCR sequences from Gamma delta (γδ) T cells; (iii) integration of therapy-related TCR-Seq datasets, such as programmed cell death 1 (PD-1) blockade immunotherapy; (iv) construction of the largest TCR sequence reference from healthy samples; and (v) redesign of a new search and download function, enabling flexible queries and downloads. With its extensive data and user-friendly web interface, TCRdb2.0 will serve as an invaluable resource for functional studies of TCRs in both health and disease.
期刊介绍:
Nucleic Acids Research (NAR) is a scientific journal that publishes research on various aspects of nucleic acids and proteins involved in nucleic acid metabolism and interactions. It covers areas such as chemistry and synthetic biology, computational biology, gene regulation, chromatin and epigenetics, genome integrity, repair and replication, genomics, molecular biology, nucleic acid enzymes, RNA, and structural biology. The journal also includes a Survey and Summary section for brief reviews. Additionally, each year, the first issue is dedicated to biological databases, and an issue in July focuses on web-based software resources for the biological community. Nucleic Acids Research is indexed by several services including Abstracts on Hygiene and Communicable Diseases, Animal Breeding Abstracts, Agricultural Engineering Abstracts, Agbiotech News and Information, BIOSIS Previews, CAB Abstracts, and EMBASE.