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- Quick Validation
- NGS-based Non-Invasive Prenatal Test
- The 100 Pathways Project
- About Us
- Whole Exome Sequencing (WES) Service
- RNA Sequencing Service (RNA-seq)
- Single Cell / Low-input RNA Sequencing Service (scRNA-seq)
In single reads, only one end of the nucleic acid fragments is sequenced. In paired-end reads, the nucleic acid fragments are first sequenced from one end, and then from the other end. This allows generation of high quality, alignable sequence data. Depending on the application, paired-end reads usually do not overlap. Paired-end reads can be used to estimate the fragment size and the duplication level of the library. In addition, paired-end sequencing allows detection of genomic rearrangements and repetitive sequence elements, as well as gene fusions and novel transcripts.
Are you ready to obtain, interpret,
and validate your NGS results in less time?