Request A Quote
Contact us to discuss how we can help you achieve your research goals

Whole Genome Sequencing

Whole Genome Sequencing (WGS) provides a deep insight into the DNA sequence of humans, animals, plants, and microbial genomes, with data analysis at the individual or population level. SNP/INDEL/CNV/SV and other variants of the genome can be fully analysed. Our sequencing analysis enables the identification of somatic and germline mutations as well as customized patterns of cancers and other diseases.


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), >99.999% (QV50) 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.