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

Annual NGS & Clinical Diagnostics, Single Cell Analysis and Genome Editing Congresses
Edinburgh Genomics will be taking part at this prestigious summit which combines 3 meetings into 1 event.    Last year saw over 600 delegates from institutions...
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Illumina and Edinburgh Genomics Whole Genome Sequencing Symposium
***REGISTRATION DEADLINE FRIDAY 22nd SEPTEMBER*** Join Illumina and Edinburgh Genomics as we showcase world-leading research applications in the comprehensive method for...
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Genome 10K and Genome Science Conference
Edinburgh Genomics is delighted to be exhibiting at the upcoming Genome 10K and Genome Science conference. Genome 10K will highlight area of research essential for...
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Vacancy: System Administrator
Edinburgh Genomics (Genome Science) is recruiting a System Administrator to join its Bioinformatics Team. Please see http://edin.ac/2uBFqec for more details.
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Customer Focus on Edinburgh Genomics
Edinburgh Genomics is a world leading genomics institution delivering cutting-edge analyses to global collaborators and customers across academia, government, and industry. Its...
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Publications

An intronic LINE-1 insertion in MERTK is strongly associated with retinopathy in Swedish Vallhund dogs Everson, R., Pettitt, L., Forman, O. P., Dower-Tylee, O., McLaughlin, B., Ahonen, S., Kaukonen, M., Komáromy, A. M., Lohi, H., Mellersh, C. S., Sansom, J. & Ricketts, S. L. 2017 In: PLoS One p. e0183021 Custom text:
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RNA substrate length as an indicator of exosome interactions in vivo Delan-Forino, C., Schneider, C. & Tollervey, D. 2017 In: Wellcome Open Research p. 34 Custom text:
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Genotype Imputation to Improve the Cost-Efficiency of Genomic Selection in Farmed Atlantic Salmon Tsai, H., Matika, O., Hoj-Edwards, S., Antolin, R., Hamilton, A., Guy, D. R., Tinch, A. E., Gharbi, K., Stear, M. J., Taggart, J. B., Bron, J. E., Hickey, J. M. & Houston, R. D. 2017 In: G3 p. 1377-1383 7 p. Custom text:
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Expression of NAD(P)H quinone dehydrogenase 1 (NQO1) is increased in the endometrium of women with endometrial cancer and women with Polycystic Ovary Syndrome Atiomo, W., Shafiee, M. N., Chapman, C., Metzler, V. M., Abouzeid, J., Latif, A., Chadwick, A., Kitson, S., Sivalingam, V. N., Stratford, I. J., Rutland, C. S., Persson, J. L., Ødum, N., Fuentes-Utrillia, P., Jeyapalan, J. N., Heery, D. M., Crosbie... 2017 In: Clinical Endocrinology Custom text:
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