Novogene’s genome sequencing service helps meet a wide range of research goals. Whole Genome Sequencing (WGS) can be applied in disease research as well as in population evolution studies. Target Capture Sequencing (TCS) can be effectively utilized for the in-depth analysis of exons (protein-coding regions of the genome) and genes of interest. As De novo sequencing offers genome assembly and annotation for seldom studied species and species with incomplete reference genomes, it provides a great advantage for plant, animal, and microbial evolution research.
80Gb - 6Tb output range, 1.6 - 40 B paired end reads per run, and PE150, PE250, PE50, etc.
N50>15kb, 90% of bases ≥Q30, 90Gb HiFi yield / SMRT Cell, 360Gb HiFi yield / run, 24-hour run times etc.
N50>15kb, read lengths up to 25kb (CCS), >99.999% (QV50) consensus accuracy, coverage across high-GC/repeat regions. HiFi reads for PacBio Sequel IIe only.
Ultra-long reads up to 2Mb, high yields for large genomes, REAL real-time and accessible for flexible budgets.
The field is required.