{"id":3189,"date":"2019-03-18T13:57:55","date_gmt":"2019-03-18T17:57:55","guid":{"rendered":"https:\/\/www.med.unc.edu\/corefacilities\/?post_type=tribe_events&p=3189"},"modified":"2019-03-21T12:16:25","modified_gmt":"2019-03-21T16:16:25","slug":"htsf-presents-illumina-wgs-sequencing-workshop","status":"publish","type":"tribe_events","link":"https:\/\/www.med.unc.edu\/corefacilities\/event\/htsf-presents-illumina-wgs-sequencing-workshop\/","title":{"rendered":"HTSF presents: Illumina WGS Sequencing Workshop"},"content":{"rendered":"

Using the Nextera\u2122 DNA Flex Library Preparation Kit on the NovaSeq6000<\/em><\/p>\n

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.
\nLearn from expert Illumina scientists as they guide you through:
\n\u2022 Library Preparation & Best Practices
\n\u2022 Experimental Design for DNA Re-Sequencing Projects
\n\u2022 Data Analysis in BaseSpace \u2122 Sequence Hub<\/p>\n

Sequencing data will be delivered by the host lab, followed by a review Q&A session with the Illumina team.<\/p>\n

Tuesday, June 4th (9am-5pm) \u2013 Wednesday, June 5th (9am-12:30pm)
\nWilson Hall Rm 134 Teaching Classroom<\/p>\n

Due to the hands-on nature of the event, space is limited to 16 participants.
\nThere is no charge to attend, however registration is required. Participation is\u00a0limited to graduate students, post-docs or faculty, but only one person per PI lab.<\/p>\n

For more information and to reserve your space, email fmoses@illumina.com<\/a> and cc wallacee@email.unc.edu<\/a><\/p>\n

* Samples must be quantified by Qubit and quality (fragmentation) assessed by Bioanalyzer, Fragment Analyzer, or gel.<\/p>\n

Participants may bring up to two DNA samples to be processed. DNA samples and their fluorometric QC*<\/p>\n","protected":false},"excerpt":{"rendered":"

Using the Nextera\u2122 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. 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