Our laboratory provides extensive support for Illumina library preparation, sequencing, and data analysis. We have well-established protocols tailored for common library preparation procedures, and our team is ready to collaborate closely with investigators with specific needs. Whether it's dealing with low input DNA or RNA quantities or custom library preparation protocols, we've got it covered.
You have the option to have your libraries undergo in-house sequencing using our Illumina MiSeq or NextSeq1000. Alternatively, for higher-throughput sequencing, we can prepare libraries for you and then send them off for sequencing elsewhere on a platform like NovaSeq. In such cases, we handle sample submission, manage data delivery logistics, and uphold strict data quality standards.
If you're unsure which Illumina sequencing platform is most suitable for your project, we've prepared a summary comparing sequence outputs (see table below). Additional details are also available on the Illumina website (https://www.illumina.com/index-d.html). Feel free to contact our MBGC staff for in-depth discussions and clarifications. We're here to assist you in making informed decisions for your research.
Illumina Library Preparation and Sequencing Submission
- Download the Illumina Illumina Library Preparation Form or the Illumina Sequencing Submission Form, and fill it in completely.
- Complete your submission using the online form:
https://rasc.osu.edu/molecular-biology-and-genomics-core/illumina-library-preparation-and-sequencing-submission
- Fill in all required fields in the webform
- Upload your completed Sample Submission Form
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Upload supporting files (e.g., sample gel images, Bioanalyzer traces, or other required documents)
Submission requests will be delayed if your form is not complete.