Abstract
Upon finishing the sequencing of the first complete human genome in 2004[1],the demand for fast DNA reading with less than$1,000 has been fueled by the ever-increasing awareness for personalized medicine and clinical diagnosis[2,3].Plenty of sequencing techniques,from the original Sanger sequencing method to novel sequencing-by-synthesis technologies(Roche,Solexa,SOLi D,etc.)[3],have been developed rapidly in past decades,which are sug-
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
