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Genome Sequencing

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.


Sequencing Platform


    NovaSeq 6000

    System specifications:

    80Gb - 6Tb output range, 1.6 - 40 B paired end reads per run, and PE150, PE250, PE50, etc.


    NovaSeq X Plus

    System specifications:

    165Gb - 16Tb output range, 3.2 - 52 B paired end reads per run, and PE50, PE100, PE150, etc.c


    PacBio Revio System

    System specifications:

    N50>15kb, 90% of bases ≥Q30, 90Gb HiFi yield / SMRT Cell, 360Gb HiFi yield / run, 24-hour run times etc.

  • PacBio

    PacBio Sequel II/IIe System

    System specifications:

    N50>15kb, read lengths up to 25kb (CCS), >99.9% (Q30) HiFi reads consensus accuracy, coverage across high-GC/repeat regions. HiFi reads for PacBio Sequel IIe only.

  • Nanopore

    Nanopore PromethION

    System specifications:

    Ultra-long reads up to 2Mb, high yields for large genomes, REAL real-time and accessible for flexible budgets.

*All specifications are available on Illumina, PacBio, and Nanopore official websites.