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For researchers preparing their own sequencing libraries, the NGS Core facility offers standalone next generation sequencing service. We also offer advice how to prepare your own sequencing libraries. Please contact us.
To choose a library preparation kit and how to pool samples you might use the Illumina Library Prep and Array Kit Selector and Index Adapters Pooling Guide.
To estimate the sequencing runs needed to reach the desired coverage for your project you might use the Illumina Coverage Calculator or the NEB Read Coverage Calculator.
Our Sequencing Only workflow provides flexible options to meet the requirements of your NGS project. We accept individual or pre-pooled libraries for sequencing on Illumina platforms, including the NovaSeq6000. Strict quality control throughout the process ensures accurate and reliable results.
Detailed information can be found in our Sample Submission and Sequencing Guidelines.
Supported Applications