地中海贫血                        
                
                                
                        
                            等位基因                        
                
                                
                        
                            遗传学                        
                
                                
                        
                            计算生物学                        
                
                                
                        
                            生物                        
                
                                
                        
                            基因                        
                
                                
                        
                            计算机科学                        
                
                        
                    
            作者
            
                Qiaowei Liang,Wanqian Gu,Ping Chen,Yuezhen Li,Yanqiu Liu,Mao Tian,Qiaomiao Zhou,Hongbo Qi,Yuhong Zhang,Jun He,Qing Li,Lingfang Tang,Juan Tang,Yanling Teng,Yulin Zhou,Sheng‐Wen Huang,Zongjie Lu,Mengnan Xu,Wei Hou,Ting Huang            
         
                    
        
    
            
            标识
            
                                    DOI:10.1016/j.jmoldx.2021.06.008
                                    
                                
                                 
         
        
                
            摘要
            
            The aim of the study was to assess the clinical utility of a third-generation sequencing (TGS) approach termed comprehensive analysis of thalassemia alleles (CATSA) for identifying both α and β thalassemia genetic carrier status. Prospective blood samples (n = 1759) with abnormal hemoglobin parameters were screened for pathogenic thalassemia variants by CATSA on the PacBio TGS platform. In 1159 individuals, a total of 1317 pathogenic thalassemia variants were identified and confirmed by independent PCR-based tests. Of the total thalassemia variants detected, the α-variant --SEA (35.4%) and β-variant c.126_129delCTTT (15%) were the most common. CATSA was also able to detect three types of rare HBA structural variants as well as five rare HBA2, three HBA1, and 10 HBB single-nucleotide variations/insertions and deletions. Compared with standard thalassemia variant PCR panel testing, CATSA identified all panel variants present, with no false-negative results. Carrier assignment was improved through identification of rare variants missed by the panel test. On the basis of allelic coverage, reliability, and accuracy, TGS with long-range PCR presents a comprehensive approach with the potential to provide a universal solution for thalassemia genetic carrier screening. It is proposed that CATSA has immediate clinical utility as an effective carrier screening approach for at-risk couples.
         
            
 
                 
                
                    
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