Sequencing

We are skilled in delivering high-quality next-generation sequencing data from RNA and DNA samples, using Illumina NovaSeq, HiSeq X and MiSeq platforms in addition to the Pacific Biosciences Sequel. 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 HiSeq X 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

Join us and learn how our PacBio Sequel platform can help support your research with long read sequencing and high consensus accuracy. Speakers will include scientific talks...
Edinburgh Genomics will close for the winter break at 5pm on Friday 21st December and will re-open at 9am on Thursday 3rd January 2019.  Customers should be aware of the...
Efforts to protect the UK's native honey bees could be helped by research that maps their entire genetic make-up. Experts also analysed the genetic profile of bacteria and...

Publications

Molecular interactions between Hel2 and RNA supporting ribosome-associated quality control Winz, M., Peil, L., Turowski, T. W., Rappsilber, J. & Tollervey, D. 2019 In: Nature Communications Custom text:
Comprehensive transcriptional profiling of the gastrointestinal tract of ruminants from birth to adulthood reveals strong developmental stage specific gene expression Bush, S., McCulloch, M., Muriuki, C., Salavati, M., Davis, G., Farquhar, I., Lisowski, Z., Archibald, A., Hume, D. & Clark, E. 2018 In: G3 Custom text:
Fibroblasts activation and abnormal extracellular matrix remodelling as common hallmarks in three cancer-prone genodermatoses Chacón-Solano, E., León, C., Díaz, F., García-García, F., García, M., Escámez, M. J., Guerrero-Aspizua, S., Conti, C. J., Mencía, Á., Martínez-Santamaría, L., Llames, S., Pévida, M., Carbonell-Caballero, J., Puig-Butillé, J. A., Maseda, R., Puig, S... 2019 In: British journal of dermatology Custom text:
De-novo mutations in patients with chronic ultra-refractory epilepsy with onset after age five years McCormack, M., McGinty, R., Zhu, X., Slattery, L., Heinzen, E. L., Costello, D. J., Delanty, N., Cavalleri, G. L. & EPIGEN Consortium 2019 In: European journal of medical genetics Custom text:
Comparative Epigenomics Reveals that RNA Polymerase II Pausing and Chromatin Domain Organization Control Nematode piRNA Biogenesis Beltran, T., Barroso, C., Birkle, T. Y., Stevens, L., Schwartz, H. T., Sternberg, P. W., Fradin, H., Gunsalus, K., Piano, F., Sharma, G., Cerrato, C., Ahringer, J., Martínez-Pérez, E., Blaxter, M. & Sarkies, P. 2019 In: Developmental Cell 24 p. Custom text:

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