Job opportunity
 Although we are currently not advertising for any open job positions at the SNP&SEQ Technology Platform you are welcome to send a spontaneous application (CV + personal letter) to:
ann-christine.syvanen@medsci.uu.se.
 We are constantly looking for experienced and skilled research engineers and bioinformaticians.

Genome Sequencer FLX (Roche/454)

Sequencing applications

  • Re-sequencing or de-novo sequencing of entire genomes
  • Transcriptome sequencing
  • Sequencing of genomic target regions. Please contact us to discuss enrichment
  • Multiplex sequencing


Our sequencing service includes

  • Preparation of libraries from gDNA or RNA for shotgun sequencing.
  • Emulsion PCR
  • Sequence runs using the Titanium 70 chemistry.
  • Delivery of sequence reads with quality information using the UPPNEX project at SNIC-UPPMAX.
  • Bioinformatics support includes data filtering, basic alignment

 

Starting material

Depending on the application the sample is DNA, RNA, or enriched DNA or PCR-products. The amount and quality of the samples is pivotal to the outcome of sequencing. The amount and quality of each sample will be verified by the SNP&SEQ platform prior to library preparation, or prior to sequencing if a library is submitted to the platform.


Amount of data generated

With the current version of instrument, software and reagents, sequencing using the Genome Sequencer FLX generates approximately 500 Mbases of sequence data per run. The reads are on average/median 400bases long (range 100-800 bases)


Delivery of data

Second generation sequence data is handled by dedicated servers equipped with large capacity redundant storage. For delivery of the large amounts of data generated by second generation sequencing we collaborate with SNIC-UPPMAX, Uppsala University's resource of high-performance computers, in the UPPNEX project. Quality controlled data will be made available via a project account created for each user at UPPNEX. The user can then perform further data analysis using the SNIC-UPPMAX compute clusters. Upon request, data can also be delivered on USB-disks or via an FTP-server.


Pricing

The cost for a sequencing project consists of the cost for library preparation including titration and emulsion PCR and that of sequencing. The cost varies with the application and the number of samples to be analysed. Please contact Ulrika Liljedahl for the specific pricing for your project.

Contact

To get access to our services, please complete a project description form and send it to our sequencing manager. For more information on our service or additional information on the different sequencing applications, please contact our sequencing manager

 

News

  • MolMed receives new grant

    2012-04-23

    Large grant for epigenetic and genomic analyses of the brain from VR, FAS, Formas and Vinnova to Molecular Medicine and the SNP&SEQ platform.

  • New sequencer, MiSeq

    2012-03-16

    The SNP&SEQ Technology Platform has installed a MiSeq instrument from Illumina.

  • The Swedish Childhood Cancer Foundation

    2011-12-14

    Molecular Medicine research group has received funding from the Swedish Childhood Cancer Foundation.

  • VR grant

    2011-11-17

    VR-RFI has granted 6.7 million SEK for running costs to the SNP&SEQ platform.

  • K&A Wallenberg grant

    2011-10-04

    Molecular Medicine research group has received funding from the K&A Wallenberg foundation.

  • Publication in Nature

    2011-08-11

    A study that doubles the number of susceptibility genes for multiple sclerosis (MS) was published in Nature on Aug 11.

  • Instrument Upgrade.

    2011-06-20

    The SNP&SEQ Technology Platform have now upgraded our Genome Analyzer IIx with a HiSeq 2000 instrument from Illumina.

  • Publication in Nature Genetics

    2011-03-06

    Five new loci for coronary artery disease were published on-line in Nature Genetics on March 6th.

  • European Project: ESGI

    2011-01-18

    The Molecular Medicine group contributes to the ESGI infra-structure by technology development, eg. allele-specific gene expression and epigenetics.