IMGT HighV-QUEST
IMGT HighV-QUEST analyzes high-throughput nucleotide sequences of immunoglobulin (IG) and T cell receptor (TR) variable domains from Next Generation Sequencing (NGS) data to identify V, D, and J genes/alleles and characterize V-REGION mutations and junctions for immunogenetics research.
Key Features:
- High-throughput NGS processing: Processes thousands of sequences simultaneously to accommodate Next Generation Sequencing datasets.
- IMGT-ONTOLOGY integration: Applies IMGT-ONTOLOGY keywords, labels, nomenclature, unique numbering, and Colliers de Perles (numerotation) for standardized description and numbering.
- Junction analysis: Incorporates IMGT/JunctionAnalysis for detailed examination of V-J and V-D-J junctions and junctional diversity.
- Automated annotation: Uses IMGT/Automat to provide complete sequence annotation of IG and TR variable domains.
- Germline alignment: Identifies V, D, and J genes and alleles by alignment to germline sequences from the IMGT reference directory.
- V-REGION mutation characterization: Characterizes V-REGION mutations and pinpoints mutation hot spots relative to the closest germline V gene.
- Diversity mechanism analysis: Analyzes combinatorial gene rearrangements (V, D, J), N-diversity (random nucleotide additions or deletions), and somatic hypermutations in IG.
- Targets IG and TR variable domains: Specifically analyzes immunoglobulin and T cell receptor variable domain sequences for repertoire studies.
Scientific Applications:
- Basic immunogenetics research: Enables analysis of adaptive immune receptor repertoires and V-REGION mutation patterns.
- Medical research and clinical diagnostics: Supports mutation analysis in contexts such as leukemia and lymphoma.
- Antibody engineering and humanization: Informs antibody design, humanization, and development of therapeutic antibodies and fusion proteins.
- Veterinary studies: Applies repertoire and mutation analyses to non-human species in veterinary research.
Methodology:
Aligns input sequences to germline sequences from the IMGT reference directory to identify V, D, and J genes and alleles; performs IMGT/JunctionAnalysis for V-J and V-D-J junction examination; uses IMGT/Automat for complete sequence annotation; applies IMGT-ONTOLOGY (keywords, labels, nomenclature, unique numbering, Colliers de Perles) for standardized description; characterizes V-REGION mutations and pinpoints mutation hot spots relative to the closest germline V gene.
Topics
Details
- Maturity:
- Mature
- Cost:
- Free of charge (with restrictions)
- Tool Type:
- web application
- Operating Systems:
- Linux, Windows, Mac
- Programming Languages:
- JavaScript, Java
- Added:
- 12/18/2019
- Last Updated:
- 11/24/2024
Operations
Publications
Lefranc M, Giudicelli V, Duroux P, Jabado-Michaloud J, Folch G, Aouinti S, Carillon E, Duvergey H, Houles A, Paysan-Lafosse T, Hadi-Saljoqi S, Sasorith S, Lefranc G, Kossida S. IMGT®, the international ImMunoGeneTics information system® 25 years on. Nucleic Acids Research. 2014;43(D1):D413-D422. doi:10.1093/nar/gku1056. PMID:25378316. PMCID:PMC4383898.
Alamyar E, Duroux P, Lefranc M, Giudicelli V. IMGT® Tools for the Nucleotide Analysis of Immunoglobulin (IG) and T Cell Receptor (TR) V-(D)-J Repertoires, Polymorphisms, and IG Mutations: IMGT/V-QUEST and IMGT/HighV-QUEST for NGS. Methods in Molecular Biology. 2012. doi:10.1007/978-1-61779-842-9_32. PMID:22665256.
V G. From IMGT-ONTOLOGY to IMGT/HighVQUEST for NGS Immunoglobulin (IG) and T cell Receptor (TR) Repertoires in Autoimmune and Infectious Diseases. Autoimmune and Infectious Diseases: Open Access ( ISSN 2470-1025 ). 2015;1(1). doi:10.16966/2470-1025.103.