Sequencing

We are skilled in delivering high-quality next-generation sequencing data from RNA and DNA samples, using Illumina HiSeq X, HiSeq 4000, HiSeq2500 and MiSeq platforms. We also regularly carry out Sanger dideoxy sequencing, using AB3730 instruments.

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Clinical Genomics WGS

Whole Genome Sequencing of samples using the Illumina HiSeqX 10 platform produces high quality data at an unprecedented speed and low cost. Laboratory automation using Illumina SeqLab platform allows very high efficiency and low variability.

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Genotyping-Arrays

High-density genotyping of pedigrees and populations, and microarray analyses of expression, binding and copy number variation are mainstays of genetic and genomic analysis. We offer genotyping and microarray gene expression analyses using Illumina and Affymetrix platforms.

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Bioinformatics

Bioinformatic analysis is at the heart of what we do, and our dedicated team of research informaticians is skilled in all aspects of next generation genomics and genetic analyses. We have an extensive, secure compute install for high-throughput data processing.

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Latest news

Edinburgh Genomics will close for the Christmas break at 5pm on Friday 23rd December and will re-open at 9am on Wednesday 4th January 2017.   Customers should be aware...
Edinburgh Genomics is a world leading genomics institution delivering cutting-edge analyses to global collaborators and customers across academia, government, and industry. Its...
Edinburgh Genomics will be hosting a User Group meeting in the Swann Lecture Theatre (King's Building campus) on Wednesday 30th November 2016. To register to attend this meeting...
Scientists at Scotland’s Rural College, together with colleagues at the University of Edinburgh and Rothamsted Research, have unravelled the genome of Ramularia, a fungal...
On June 3rd 2016, our Clinical Division hosted a visit by NHS Scotland and the Chief Scientist Office. This was an opportunity to see for themselves the Edinburgh Genomics high...

Publications

The antiviral RNAi response in vector and non-vector cells against orthobunyaviruses Dietrich, I., Shi, X., McFarlane, M., Watson, M., Blomström, A., Skelton, J. K., Kohl, A., Elliott, R. M. & Schnettler, E. 2017 In: PLoS Neglected Tropical Diseases Custom text:
The incredible complexity of RNA splicing Robert, C. & Watson, M. 2016 In: Genome Biology Custom text:
Circulating Plasma microRNAs can differentiate Human Sepsis and Systemic Inflammatory Response Syndrome (SIRS) Caserta, S., Kern, F., Cohen, J., Drage, S., Newbury, S. F. & Llewelyn, M. J. 2016 In: Scientific Reports p. 28006 Custom text:
Extension of human lncRNA transcripts by RACE coupled with long-read high-throughput sequencing (RACE-Seq) Lagarde, J., Uszczynska-Ratajczak, B., Santoyo-Lopez, J., Gonzalez, J. M., Tapanari, E., Mudge, J. M., Steward, C. A., Wilming, L., Tanzer, A., Howald, C., Chrast, J., Vela-Boza, A., Rueda, A., Lopez-Domingo, F. J., Dopazo, J., Reymond, A., Guigó, R... 2016 In: Nature Communications Custom text:
New challenges for BRCA testing: a view from the diagnostic laboratory Wallace, A. J. 2016 In: European Journal of Human Genetics p. S10-8 Custom text:

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