HTSF presents: Illumina WGS Sequencing Workshop

Using the Nextera™ DNA Flex Library Preparation Kit on the NovaSeq6000

Please join us for a hands-on experience of our latest and fast, comprehensive DNA re-sequencing workflow, using your own samples on the NovaSeq6000.
Learn from expert Illumina scientists as they guide you through:
• Library Preparation & Best Practices
• Experimental Design for DNA Re-Sequencing Projects
• Data Analysis in BaseSpace ™ Sequence Hub

Sequencing data will be delivered by the host lab, followed by a review Q&A session with the Illumina team.

Tuesday, June 4th (9am-5pm) – Wednesday, June 5th (9am-12:30pm)
Wilson Hall Rm 134 Teaching Classroom

Due to the hands-on nature of the event, space is limited to 16 participants.
There is no charge to attend, however registration is required. Participation is limited to graduate students, post-docs or faculty, but only one person per PI lab.

For more information and to reserve your space, email fmoses@illumina.com and cc wallacee@email.unc.edu

* Samples must be quantified by Qubit and quality (fragmentation) assessed by Bioanalyzer, Fragment Analyzer, or gel.

Participants may bring up to two DNA samples to be processed. DNA samples and their fluorometric QC*