Your browser doesn't support javascript.
loading
Validation of a mobile phone-assisted microarray decoding platform for signal-enhanced mutation detection.
Zhang, Guanbin; Li, Caixia; Lu, Yuan; Hu, Hua; Xiang, Guangxin; Liang, Zhiqing; Liao, Pu; Dai, Pu; Xing, Wanli; Cheng, Jing.
Afiliação
  • Zhang G; Medical Systems Biology Research Center, School of Medicine, Tsinghua University, Beijing, China.
Biosens Bioelectron ; 26(12): 4708-14, 2011 Aug 15.
Article em En | MEDLINE | ID: mdl-21676608
ABSTRACT
We have established a mobile phone-assisted microarray decoding platform for signal-enhanced mutation detection. A large amount of single-stranded DNA (ssDNA) was obtained by combining symmetric PCR and magnetic isolation, and ssDNA prepared with magnetic bead as label was further allowed to hybridize against the tag-array for decoding purpose. High sensitivity and specificity was achieved with the detection of genomic DNA. When simultaneously genotyping nine common mutations associated with hereditary hearing loss, the detection limit of 1 ng genomic DNA was achieved. Significantly, a mobile phone was also used to record and decode the genotyping results through a custom-designed imaging adaptor and a dedicated mobile phone software. A total of 51 buccal swabs from patients probably with deafness-related mutations were collected and analyzed. The genotyping results were all confirmed by fluorescence-based laser confocal scanning and direct DNA sequencing. This mobile phone-assisted decoding platform provides an effective but economic mutation detection alternative for the future quicker and sensitive detection of virtually any mutation-related diseases in developing and underdeveloped countries.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: DNA de Cadeia Simples / Análise de Sequência com Séries de Oligonucleotídeos / Telefone Celular / Perda Auditiva / Mutação Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Ano de publicação: 2011 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: DNA de Cadeia Simples / Análise de Sequência com Séries de Oligonucleotídeos / Telefone Celular / Perda Auditiva / Mutação Tipo de estudo: Diagnostic_studies Limite: Humans Idioma: En Ano de publicação: 2011 Tipo de documento: Article