Paired-end sequencing is defined as a process to sequence both ends of the fragment and to generate high sequence data. Paired-end sequencing detects the genomic rearrangement, repetitive sequence elements, gene fusion and novel transcripts. Since paired-end reads are more likely to align to a reference, the quality of the entire data set improves. All Illumina NGS (next-generation sequencing) systems are capable of paired-end sequencing. Paired-end DNA sequencing reads provide superior alignment across DNA regions containing repetitive sequences, and produce longer contigs for de novo sequencing by filling gaps in the consensus sequence.
Related Journals of Paired-End Sequencing
Journal of Next Generation Sequencing & Applications, Advancements in Genetic Engineering, Journal of Computer Science & Systems Biology, Journal of Proteomics & Bioinformatics, Transcriptomics: Open Access, Journal of Bioinformatics and Sequence Analysis, Sequencing Oxford Journals, International Journal of Paired Sequencing, European Journal of Paired Sequencing, Bioinformatics Journal of Sequencing.
