KCCG Sequencing Laboratory

Delivering research sequencing and data analysis at scale

Clinically accredited scalable sequencing

Our sequencing is carried out in an ISO15189-accredited laboratory.

Award-winning variant calling pipeline

Our genome analytics pipeline was awarded the highest SNP precision in the precisionFDA Truth Challenge in 2016*

Custom bioinformatics services

Access our team of bioinformatics experts and our software solutions to accelerate your genomic analyses

Performance of quality deliverables 

≥75% bases above Q30 guaranteed (If sample meets minimum requirements)
Over 30x coverage for human DNA (WGS)

These graphs indicate our quality performance from filtered data of >20,000 genomes run to date:


Fast turnaround

Turnaround time from 6 weeks dependent on service required.

Flexible and customisable service

Benefit from our expert consultant service to design your project and select the services best suited to your project needs

Wide range of services

Our expert capabilities with the Illumina HiSeq X and NovaSeq 6000 allows us to offer a range of sequencing services covering all species, scaled to suit individual projects, all run through the ISO15189-accredited laboratory. Our team can offer assistance to ensure the sequencing selected best answers your projects question.


Sample preparation

  • TruSeq Nano DNA Library Preparation
  • KAPA Hyper PCR-Free Library Preparation 
  • Chromium Genome Solution Library Preparation 
  • Agilent SureSelect Exome Library Preparation
  • Researcher Submitted Library 


  • Whole Genome Sequencing
  • Whole Exome Sequencing 
  • Targeted Sequencing
  • Single-cell RNA-Seq 
  • Transcriptomics
  • DeNovo Sequencing 
  • Linked-read sequencing 

We are happy to discuss other applications of the genomic sequencing service to try and fit your needs.

Project matched scalability

The range of sequencing platforms, in combination with laboratory automation, are capable of processing tens of thousands of samples a year. 

With our portfolio of platforms we can process any batch size - from single sample to population scale projects.

Secure data transfer and delivery options

 We utilise the DNAnexus platform for online data delivery. DNAnexus provides clinical-grade security and privacy and is compliant with HIPAA, CLIA, ISO27001, dbGaP and EU Privacy regulations

Structural variation and CNVs 

Chromosomal modifications, such as translocations and inversions, can be precisely defined by WGS, often with single-nucleotide precision. Consistent genome-wide coverage provided by WGS also makes it straightforward to call CNVs through the NATA accredited CNV pipeline.

*This award is not an endorsement by the U.S. FDA of our product and services.