Targeted sequencing services

Targeted sequencing involves sequencing a small region or set of regions of the genome, such as particular chromosomes, exomes, or individual genes of scientific or clinical interest.

This provides a highly cost effective alternative to whole genome sequencing, especially when only a small portion of the genome is required. Due to the smaller size of the regions targeted sequencing captures, deeper sequencing can be performed at a lower cost, ensuring rare and novel mutations are captured by the sequencing.

Targeted sequencing can be performed on a wide variety of species to observe specific intronic and exonic regions, this is especially useful when analysing mutations in model organisms such as C. elegans.

This technique is also a popular approach to sequence many individuals in order to discover, screen or validate genetic variation within a population.

Targeted sequencing is at the forefront of cancer research and treatment. By sequencing known genes of clinical relevance, mutations can be detected which may interfere with a particular treatment, allowing oncologists to select a more effective therapy.

A variety of options are available for targeted sequencing:

  • Custom designed targeted enrichment
  • Next-generation sequencing panels
  • Exome Sequencing
  • Amplicon sequencing


Exome Sequencing Service | Source BioScience

A complete exome sequencing service designed to enrich and capture exonic regions of interest in the human genomeView >

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Interested in using our next-generation sequencing service? For more information, a competitive quotation or simply help and support for your research, please call or email us.