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High-Throughput Immunogenetics for Clinical and Research Applications in Immunohematology: Potential and Challenges
Author(s) -
Anton W. Langerak,
Monika Brüggemann,
Frédéric Davi,
Nikos Darzentas,
Jacques J. M. van Dongen,
David González,
Giovanni Cazzaniga,
Véronique Giudicelli,
MariePaule Lefranc,
Mathieu Giraud,
Elizabeth Macintyre,
Michael Hummel,
Christiane Pott,
Patricia J.T.A. Groenen,
Κώστας Σταματόπουλος
Publication year - 2017
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.1602050
Subject(s) - computational biology , workflow , throughput , dna sequencing , computer science , biology , gene , genetics , database , telecommunications , wireless
Analysis and interpretation of Ig and TCR gene rearrangements in the conventional, low-throughput way have their limitations in terms of resolution, coverage, and biases. With the advent of high-throughput, next-generation sequencing (NGS) technologies, a deeper analysis of Ig and/or TCR (IG/TR) gene rearrangements is now within reach, which impacts on all main applications of IG/TR immunogenetic analysis. To bridge the generation gap from low- to high-throughput analysis, the EuroClonality-NGS Consortium has been formed, with the main objectives to develop, standardize, and validate the entire workflow of IG/TR NGS assays for 1) clonality assessment, 2) minimal residual disease detection, and 3) repertoire analysis. This concerns the preanalytical (sample preparation, target choice), analytical (amplification, NGS), and postanalytical (immunoinformatics) phases. Here we critically discuss pitfalls and challenges of IG/TR NGS methodology and its applications in hemato-oncology and immunology.

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