The EASIH operates instrumentation from all three of the major next-gen sequencing vendors. This allows us to provide a wide range of sequencing applications to fit your scientific needs. We can offer mate paired reads, single or paired end reads and multiplexing if you have a large number of samples. Some of the sequencing applications that we can offer are:
- Whole genome resequencing
- Variation detection
- Targeted resequencing
- De novo assembly (bacterial / yeast size genomes)
- Small RNA discovery and quantitation of known small RNAs and novel transcripts.
- Tag profiling
- DNAseI hypersensitivity
- Nucleosome mapping
- Amplification free transcriptome analysis (FRT-seq)
- Serial Analysis of Gene Expression (SAGE) mapping
If there is something you are interested in that isn't listed please contact us to discuss how we can develop our service to meet your needs.
For platform specific information on the services we can offer please click on the vendors logos above to view their individual websites.
In collaboration with the East Anglian Medical Genetics Service and National Blood Service EASIH won a honorary prize in the Ion Torrent competition and can now offer sequencing on this exciting new platform!
EASIH also acquired a Roche GS Junior which is suited to de novo genome sequencing, metagenomic analysis and in particular amplicon sequencing.