MedElevator Войти в исследования
← Поиск публикаций

DOI 10.1002/humu.21322

Медицинская библиотека · Human mutation · 2010

A custom 148 gene-based resequencing chip and the SNP explorer software: new tools to study antibody deficiency.

Wang Hong-Ying, Gopalan Vivek, Aksentijevich Ivona, Yeager Meredith, Ma Chi Adrian, Mohamoud Yasmin Ali, Quinones Mariam, Matthews Casey, Boland Joseph, Niemela Julie E, Torgerson Troy R, Giliani Silvia, Uzel Gulbu, Orange Jordan S, Shapiro Ralph, Notarangelo Luigi, Ochs Hans D, Fleisher Thomas, Kastner Daniel, Chanock Stephen J, Jain Ashish

СтатьяResearch Support, N.I.H., IntramuralПеревод пока не подготовлен

Аннотация

Hyper-IgM syndrome and Common Variable Immunodeficiency are heterogeneous disorders characterized by a predisposition to serious infection and impaired or absent neutralizing antibody responses. Although a number of single gene defects have been associated with these immune deficiency disorders, the genetic basis of many cases is not known. To facilitate mutation screening in patients with these syndromes, we have developed a custom 300-kb resequencing array, the Hyper-IgM/CVID chip, which interrogates 1,576 coding exons and intron-exon junction regions from 148 genes implicated in B-cell development and immunoglobulin isotype switching. Genomic DNAs extracted from patients were hybridized to the array using a high-throughput protocol for target sequence amplification, pooling, and hybridization. A Web-based application, SNP Explorer, was developed to directly analyze and visualize the single nucleotide polymorphism (SNP) annotation and for quality filtering. Several mutations in known disease-susceptibility genes such as CD40LG, TNFRSF13B, IKBKG, AICDA, as well as rare nucleotide changes in other genes such as TRAF3IP2, were identified in patient DNA samples and validated by direct sequencing. We conclude that the Hyper-IgM/CVID chip combined with SNP Explorer may provide a cost-effective tool for high-throughput discovery of novel mutations among hundreds of disease-relevant genes in patients with inherited antibody deficiency.

Для цитирования: Wang Hong-Ying, Gopalan Vivek, Aksentijevich Ivona, Yeager Meredith, Ma Chi Adrian, Mohamoud Yasmin Ali, Quinones Mariam, Matthews Casey, Boland Joseph, Niemela Julie E, Torgerson Troy R, Giliani Silvia, Uzel Gulbu, Orange Jordan S, Shapiro Ralph, Notarangelo Luigi, Ochs Hans D, Fleisher Thomas, Kastner Daniel, Chanock Stephen J, Jain Ashish. A custom 148 gene-based resequencing chip and the SNP explorer software: new tools to study antibody deficiency.. Human mutation. 2010. DOI: 10.1002/humu.21322.

Предметные рубрики MeSH

Подготовка и перевод публикации
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…

История · было → стало

Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.

Тип публикации указан по данным источника. Уровень доказательности автоматически не присваивается.