Next Generation Sequencing Seminars Open Access Journals

 The massively parallel sequencing technology referred to as next-generation sequencing (NGS) has revolutionized the biological sciences. With its ultra-high throughput, speed and scalability next-generation sequencing enables researchers to perform a good sort of applications and study biological systems at A level never before possible.   Today's complex genomic research questions demand a depth of data beyond the capacity of traditional DNA sequencing technologies. Next-generation sequencing has filled that gap and become an everyday research tool to deal with these questions. Advantages of Next-generation sequencing include Higher sensitivity to detect low-frequency variants. Faster turnaround time for high sample volumes. Comprehensive genomic coverage. To perform Sanger Sequencing, you add your primers to a solution containing the genetic information to be sequenced, then divide up the solution into four PCR reactions. Each reaction contains a with dNTP mix with one among the four nucleotides substituted with a ddNTP (A, T, G, and C ddNTP groups). The key difference between current next generation sequencing techniques is the targeted enrichment step where gene panels focus on a limited number of genes; whole exome sequencing is focused on protein coding regions (~1−2% of the genome) and whole genome sequencing does not require targeted enrichment. Next generation methods of DNA sequencing have three general steps: Library preparation: libraries are created using random fragmentation of DNA, followed by ligation with custom linkers. Amplification: the library is amplified using clonal amplification methods and PCR.