Pricing does not reflect discounts offered to affiliates of certain research units or of specific center grants. Special project pricing may be available upon request.
||UofM Rates per well
||External Non-Profit Rates per well
|Ruch (Next Day)
One sequencing run (one template, one primer) typically produces 900 nucleotides of high-quality sequence data or more, for a good quality template and a well-designed primer.
Login through https://client-seqcore.brcf.med.umich.edu and then choose “Sanger Sequencing” to submit samples.
For our recommended template and primer concentrations, please go to faq page for Sanger Sequencing and read FAQ #17.
Samples are usually processed within two business days after receipt.
The results are returned in two forms: a raw sequence file and a chromatogram file. The sequence file (a flat ASCII text file) is returned to the researcher by electronic mail. The chromatogram file is available on our data server (password protected to prevent unauthorized distribution of your data).
Chromatograms and text files are available for download for 2 weeks after sequencing has been completed from our FTP server, after which the data is auto-deleted. The DNA Sequencing Core keeps all old sequencing data in archival storage, and can retrieve the data upon request by putting it on our FTP server. It will however be auto-deleted after 2 weeks. For more information on Sanger Sequencing please go to the FAQ page.