We are Illumina Propel certified and have vast experience in sequencing all types of challenging libraries including ATACseq, low diversity libraries, Amplicon Sequencing, sequencing with custom primers, Fluidigm libraries and Bisulfite converted libraries.

We offer short read sequencing services on Illumina HiSeq2500 and MiSeq and long read sequencing on GridIon.

Our researchers have the flexibility of preparing their own libraries and using our sequencing services alone or using our library preparation services in concert with sequencing.

We are Illumina Propel certified and have vast experience in sequencing all types of challenging libraries including ATACseq, low diversity libraries, Amplicon Sequencing, sequencing with custom primers, Fluidigm libraries and Bisulfite converted libraries.

We aim to provide data to researchers in a usable format by supporting data analysis for short read libraries prepared and sequenced in our lab. Please refer to our data analysis pages to check our integrated data analysis services.

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Researchers are expected to discuss data analysis requirements at the project discussion stage. For libraries prepared elsewhere and sequenced on the Illumina platform in our lab, we provide access to Partek Flow and Partek Genomics suite software. Researchers are required to book access to Partek Flow at the time of initial request on iLabs.

To access this service, initiate a sequencing request via iLabs. You will first need to register with iLabs.

To discuss how we can help you with your project, please contact BRC.Genomics@gstt.nhs.uk.