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Long-read transcriptome sequencing reveals allele-specific variants at high resolution.
Wu, Jingni; Hu, Wei; Li, Shengli.
Afiliação
  • Wu J; Precision Research Center for Refractory Diseases, Institute for Clinical Research, Shanghai Jiao Tong University School of Medicine, Shanghai 201620, China.
  • Hu W; Precision Research Center for Refractory Diseases, Institute for Clinical Research, Shanghai Jiao Tong University School of Medicine, Shanghai 201620, China; Ministry of Education (MOE) Key Laboratory of Metabolism and Molecular Medicine, Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Fudan University, Shanghai, China.
  • Li S; Precision Research Center for Refractory Diseases, Institute for Clinical Research, Shanghai Jiao Tong University School of Medicine, Shanghai 201620, China. Electronic address: shengli.li@sjtu.edu.cn.
Trends Genet ; 39(1): 31-33, 2023 01.
Article em En | MEDLINE | ID: mdl-36207147
ABSTRACT
Disturbance in the regulation of transcript structure plays a crucial role in human disease. In a recent study, Glinos et al. characterized allele-specific transcript alterations in long-read RNA sequencing (RNA-seq) data derived from multiple human tissues and provide a high-resolution view of how disease-associated genetic variants affect transcript structure.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: RNA / Transcriptoma Limite: Humans Idioma: En Revista: Trends Genet Assunto da revista: GENETICA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Base de dados: MEDLINE Assunto principal: RNA / Transcriptoma Limite: Humans Idioma: En Revista: Trends Genet Assunto da revista: GENETICA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: China