Dept. of Medical Genetics Ullevål
Kirkeveien 166 (map)
Follow us on twitter.
Illumina’s lastest sequencers, HiSeq X, HiSeq 4000 and HiSeq 3000 have now been purchased and are being installed at the NSC.
HiSeq X is targeted at population-scale genome sequencing and NSC now has 4 of these machines. The first has been installed and tested. We expect the remaining 3 machines to be operational before summer.
HiSeq 3000 and 4000 build upon the existing HiSeq 2500 platform using the new HiSeq X patterned flow cell technology. The principle benefit to users will be faster turnaround time (run time is 3 days compared to 6 days in HiSeq 2500). Also, the new patterned flow cell will provide higher quality and more data per run and longer reads (150 bp paired end compared to existing 125 bp paired end).
To keep up with the ever-growing demand for NextSeq, NSC has purchased a second machine and this has been operational since Jan 2016.
With the purchase of the above machines, NSC now has the complete range of Illumina sequencers - HiSeq X, HiSeq 3000/4000, HiSeq 2500, NextSeq 500 and MiSeq available for all types of sequencing solutions!
More about HiSeqX: Illumina HiSeqX
More about HiSeq 4000 and 3000: Illumina HiSeq 4000/3000
Illumina's latest sequencer model, the NextSeq 500, is now operational at the NSC. With up to 800 million 150 bp reads per 2-day run, the NextSeq bridges the output gap between the HiSeq and MiSeq instruments.
We're now offering Illumina's V4 chemistry as standard on our HiSeqs. That means more reads (150-250 million per end, per lane), and longer reads too - now 125 bp. Perhaps most importantly, run times have been reduced from 12 days to 6, knocking a week off turnaround time.
We are now sequencing several thousand samples per year, and have realised for some time the need for sample tracking software. After extensive validation, we have purchased Genologics Clarity LIMS (http://www.genologics.com/ We will be implementing this over the next months, to ensure your samples are handled in the most secure and timely manner possible.
ForBio (www.forbio.uio.no) announces a course relevant for NSC users: Introduction to Bioinformatics for Biosystematics.
The Norwegian Research Council announced last week that the Norwegian Sequencing Centre (NSC) gets 41 MNOK of funding from 2014.