Whole Genome Sequencing

Long read enriched sequencing!

Whole-genome sequencing (WGS) is a comprehensive method for analyzing entire genomes. Genomic information has been instrumental in identifying inherited disorders, characterizing the mutations that drive cancer, and predicting outbreaks. The ability to produce large volumes of data with our technology makes whole-genome sequencing a powerful tool for genomics research. This method is not only associated with sequencing human genomes, but also the sequencing technology we use makes it equally useful for sequencing any species, such as agriculturally important livestock, plants, or pathogenic microbes.

a bigger picture for a more thorough analysis

Unlike focused approaches such as whole exome or targeted resequencing, which analyze a targeted part of the genome, whole-genome sequencing gives an insightful full view of the entire genome. It is ideal for discovery applications, such as identifying causative variants and novel genome assembly. Whole-genome sequencing can detect single nucleotide variants, insertions/deletions, copy number changes, and large structural variants.
We offer the following types of whole genome sequencing:

  1. Large Whole-Genome Sequencing:
    Sequencing large genomes (> 5 Mb), such as human, plant, or animal genomes, which can provide valuable information for disease research and population genetics.
  2. Small Whole-Genome Sequencing
    Small genome sequencing (≤ 5 Mb) involves sequencing the entire genome of a bacterium, virus, or other microbe, without requiring bacterial culture.
  3. De Novo Sequencing:
    De novo sequencing refers to sequencing a novel genome where there is no reference sequence available.

Coupled with our strong cloud computing powers, we provide data results and analysis in extremely fast times. We also use our own in house developed Artificial intelligence algorithms for strong, fast and reliant gene assembly and alignmen

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