Long-read sequencing
Long Read Sequencing (LRS) service employs cutting-edge technologies such as Oxford Nanopore and PacBio platforms for decoding complex genomes, completing transcriptomes, exploring metagenomes, and investigating structural variations with unmatched precision.

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Novogene's long-read sequencing service offers:
- Comprehensive genome analysis of assembly and annotation
- Full-length transcripts exploration to unveil intricate isoform diversity
- Metagenome-assembled genomes (MAGs) analysis to capture the full length of 16S/18S/ITS sequencing for previously hidden genetic diversity
- Detect and characterize structural variations, inversions, and rearrangements in genomes with unparalleled accuracy













