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Whole Genome Sequencing

Whole Genome Sequencing (WGS) refers to the process of determining the complete DNA sequence of an organism’s genome. This method provides a detailed analysis of both coding and non-coding regions, enabling comprehensive insights into the genetic makeup of humans, animals, plants, and microbial species. By examining the entire genome, WGS identifies a broad spectrum of genetic variations, including single nucleotide polymorphisms (SNPs), insertions and deletions (INDELs), copy number variations (CNVs), and structural variations (SVs). Our sequencing analysis enables the identification of somatic and germline mutations as well as customized patterns of cancers and other diseases.

Technology

Sequencing Platform

  • ILLUMINA

    NovaSeq 6000

    System specifications:

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

  • ILLUMINA

    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

    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 IIe System

    System specifications:

    N50>15kb, read lengths up to 25kb (CCS), >99.999% (QV50) consensus accuracy, coverage across high-GC/repeat regions.

  • Nanopore

    Nanopore PromethION

    System specifications:

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