KCCG Sequencing Laboratory
The KCCG Sequencing Laboratory offers clinically accredited, scalable sequencing and expert genomic analysis. We tailor sequencing and analysis solutions to suit your needs – from small research studies to large-scale populations and cohorts.
Our expert team have experience with a diverse range of projects, and can help design a custom service that matches your goals.
Contact us at firstname.lastname@example.org to find out how we can help with your project.
Clinically accredited sequencing
All sequencing is performed in our ISO17025-accredited laboratory (with no clinical reporting).
Our genome analytics pipeline was awarded the highest SNP precision in the precisionFDA Truth Challenge in 2016*
Collaborative, flexible service
Access our complete sequencing and analysis infrastructure, and work with our experts to build custom genomic analyses
*This award is not an endorsement by the U.S. FDA of our product and services.
How it works
Complete online manifest
Submit samples & documents
Our cohort sequencing and custom bioinformatics services can be applied to a diverse range of projects
These data are from the Coriell Cell Repository NA12878 reference cell line, which has been extensively analysed by the Genome in a Bottle Consortium. The sequencing libraries were generated with Illumina’s TruSeq Nano V2.5 kit using the Hamilton Microlab STAR robotics platform, achieving >400bp inserts. Each library was sequenced on a single lane of an Illumina HiSeq X patterned flow cell, achieving over 130Gb of yield, with > 83% of bases with quality > Q30 in just 2.8 days. The four data sets are of similar quality, and are provided to allow you to assess the reproducibility of the technology. Each data set substantially surpasses the minimum coverage and quality guaranteed by Illumina and is indicative of the potential for the Illumina HiSeq X sequencing system.
Each of the four datasets consists of raw paired-end data (fastq.gz files) and results obtained with the GATK DNAseq best practices pipeline run on each library independently with the recommended parameters for whole genome sequencing.
Download the data to your computer or server, using the links in these tables.