T细胞受体
计算生物学
序列(生物学)
序列分析
基因
免疫球蛋白结构域
生物
序列比对
遗传学
T细胞
计算机科学
肽序列
免疫系统
出处
期刊:Journal of Immunology
[The American Association of Immunologists]
日期:2016-05-01
卷期号:196 (1_Supplement): 138.3-138.3
被引量:1
标识
DOI:10.4049/jimmunol.196.supp.138.3
摘要
Abstract The variable domain of B and T cell receptor is encoded by multiple genes, including the variable (V) gene, the diversity (D) gene and the joining (J) gene. Previously we developed an analysis tool, IgBLAST, for immunoglobulin sequences (http://www.ncbi.nlm.nih.gov/igblast/). Here we describe our recent update on this tool. The new functionalities include capability to analyze T cell receptor sequences (TR), annotating the CDR3 region, extending alignment to 5′ end of the V region, more flexibility in search criteria and providing summarized information to aid large-scale sequence analysis. We use examples to demonstrate these new functionalities and their implications in Ig and TCR sequence analysis.
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