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For researchers which do not have the possibility to provide ready-to-sequence libraries, the NGS core facility offers a full service from nucleic acids, single cell or single nuclei to sequencing data. Researcher send the samples to NGS core facility where the samples will be processed in the wet lab and sequenced.
To estimate the sequencing runs needed to reach the desired coverage for your project you might use the Illumina Coverage Calculator.
All DNA and RNA samples (either sent by you or after isolation at our facility) will go through a standardized quality control protocol.
Detailed information can be found in our Sample Submission and Sequencing Guidelines.