huARdb: human Antigen Receptor database for interactive clonotype-transcriptome analysis at the single-cell level.
huARdb: human Antigen Receptor database for interactive clonotype-transcriptome analysis at the single-cell level.
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huARdb:用于单细胞水平交互式克隆型转录组分析的人类抗原受体数据库。
DOI:
10.1093/nar/gkab857
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发表时间:
2022-01-07
影响因子:
14.9
通讯作者:
Liu W
中科院分区:
文献类型:
--
作者:
Wu L;Xue Z;Jin S;Zhang J;Guo Y;Bai Y;Jin X;Wang C;Wang L;Liu Z;Wang JQ;Lu L;Liu W
T-cell receptors (TCRs) and B-cell receptors (BCRs) are critical in recognizing antigens and activating the adaptive immune response. Stochastic V(D)J recombination generates massive TCR/BCR repertoire diversity. Single-cell immune profiling with transcriptome analysis allows the high-throughput study of individual TCR/BCR clonotypes and functions under both normal and pathological settings. However, a comprehensive database linking these data is not yet readily available. Here, we present the human Antigen Receptor database (huARdb), a large-scale human single-cell immune profiling database that contains 444 794 high confidence T or B cells (hcT/B cells) with full-length TCR/BCR sequence and transcriptomes from 215 datasets. All datasets were processed in a uniform workflow, including sequence alignment, cell subtype prediction, unsupervised cell clustering, and clonotype definition. We also developed a multi-functional and user-friendly web interface that provides interactive visualization modules for biologists to analyze the transcriptome and TCR/BCR features at the single-cell level. HuARdb is freely available at https://huarc.net/database with functions for data querying, browsing, downloading, and depositing. In conclusion, huARdb is a comprehensive and multi-perspective atlas for human antigen receptors.
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影响因子:
5.4
作者:
Fraser LD;Zhao Y;Lutalo PM;D'Cruz DP;Cason J;Silva JS;Dunn-Walters DK;Nayar S;Cope AP;Spencer J
通讯作者:
Spencer J
DOI:
10.4049/jimmunol.1100657
发表时间:
2012-01-01
期刊:
Journal of immunology (Baltimore, Md. : 1950)
影响因子:
--
作者:
Alli R;Nguyen P;Boyd K;Sundberg JP;Geiger TL
通讯作者:
Geiger TL
影响因子:
64.8
作者:
Harris CR;Millman KJ;van der Walt SJ;Gommers R;Virtanen P;Cournapeau D;Wieser E;Taylor J;Berg S;Smith NJ;Kern R;Picus M;Hoyer S;van Kerkwijk MH;Brett M;Haldane A;Del Río JF;Wiebe M;Peterson P;Gérard-Marchant P;Sheppard K;Reddy T;Weckesser W;Abbasi H;Gohlke C;Oliphant TE
通讯作者:
Oliphant TE
影响因子:
7.3
作者:
D'Angelo S;Ferrara F;Naranjo L;Erasmus MF;Hraber P;Bradbury ARM
通讯作者:
Bradbury ARM
影响因子:
4.3
作者:
Fujii M;Nishida A;Imaeda H;Ohno M;Nishino K;Sakai S;Inatomi O;Bamba S;Kawahara M;Shimizu T;Andoh A
通讯作者:
Andoh A