{"id":499,"date":"2022-08-10T11:22:10","date_gmt":"2022-08-10T15:22:10","guid":{"rendered":"https:\/\/research.ncsu.edu\/gsl\/?page_id=499"},"modified":"2025-06-13T13:47:15","modified_gmt":"2025-06-13T17:47:15","slug":"sponsored-projects","status":"publish","type":"page","link":"https:\/\/research.ncsu.edu\/gsl\/news\/sponsored-projects\/","title":{"rendered":"GSL Sponsored Seminars & Events"},"content":{"rendered":"\n\n\n\n\n

2020<\/h2>\n\n\n\n

CLC Genomics Training Workshop<\/strong><\/h3>\n\n\n
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\n Sponsored by the NC State Genetics & Genomics Initiative<\/a>, the Center for Human Health and the Environment<\/a>, and the NC State Genomic Sciences Laboratory<\/a>.<\/strong>\n <\/p>\n \n

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Thursday, January 30th from 9:30 AM-3:30 PM (l<\/strong>unch provided if registered<\/a>).<\/strong><\/h3>\n\n\n\n

Stephens Room (Room 3503), Thomas Hall, Main Campus<\/strong><\/h3>\n\n\n\n

9:30 \u2013 10:15 AM:<\/strong> Installing CLC, connecting to your network, how to connect to the HPC, Introduction to Qiagen Bioinformatic Solutions<\/p>\n\n\n\n

10:30 \u2013 12:00 PM:<\/strong> RNA-seq data analysis<\/p>\n\n\n\n

12:00-1:00 PM: LUNCH  <\/strong>** Lunch will be provided to registered participants **<\/p>\n\n\n\n

1:00-2:15 PM: <\/strong>Microbiome analysis: 16S\/shotgun sequencing<\/p>\n\n\n\n

2:30-3:30 PM: <\/strong>Genome and Metagenome assembly<\/p>\n\n\n\n

See Event Flyer<\/a> for more information.<\/p>\n\n\n

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2019<\/h2>\n\n\n\n
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10X Genomics & Illumina Joint Seminar<\/h3>\n\n\n\n

Hosted by the NC State Genomic Sciences Laboratory and the Genetics & Genomics Initiative<\/h4>\n\n\n\n

Wednesday, December 4th from 10 AM \u2013 12 PM in the Stephens Room (3503 Thomas Hall). Refreshments Provided.<\/h3>\n\n\n\n

Please REGISTER<\/strong> for this event here<\/a>.<\/h4>\n\n\n\n

10:00-11:00am<\/strong> \u2013 Nirav Patel, MS, Science & Technology Advisor, 10x Genomics \u2013 \u201cResolving Biology with Single Cell multi-omics and Spatial Transcriptomics\u201d<\/h4>\n\n\n\n

11:00-12:00pm<\/strong>\u2013 Matt Angel, Executive Sequencing & Data Analysis Specialist, Illumina \u2013 \u201cSequencing Considerations of Single Cell Analysis & Emerging Applications\u201d<\/h4>\n\n\n\n

See Event Flyer<\/a> for more information.<\/p>\n\n\n

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Illumina DNA Workshop Using the Nextera\u2122 DNA Flex Library Preparation Kit on the NovaSeq 6000<\/h3>\n\n\n\n
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THIS WORKSHOP IS CURRENTLY FULL \u2013 Please email us for inquiries on waitlisting for future workshops.<\/h3>\n\n\n\n

Hosted by the NCSU BIT Program and the Genomic Sciences Laboratory<\/h4>\n\n\n\n

Wednesday, August 14th (9am-4pm) \u2013 Thursday, August 15th (9am-12:00pm); Jordan Hall Lab Room 6136<\/h4>\n\n\n\n

Please join us for a hands on experience of our easy and efficient, Nextera DNA Flex Library Prep workflow for WGS of any genome, using your own samples on the GSL NovaSeq 6000. Learn from expert Illumina scientists as they guide you through: Library Preparation & Best Practices, Experimental Design for DNA sequencing Projects, and Data Analysis in BaseSpace\u2122Sequence Hub. Sequencing data will be delivered by the Genomic Sciences Laboratory, followed by a review Q&A session with the Illumina workshop team.<\/p>\n\n\n

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Whole Genome Sequencing Technologies using Oxford Nanopore Technologies to enable high quality reference genomes.<\/h3>\n\n\n\n

Presented by Nick Beckloff, Ph.D., FAS<\/p>\n\n\n\n

Wednesday, May 8th from 1:30-3:00 PM (Stephens Room \u2013 3503 Thomas Hall).<\/h4>\n\n\n\n

Hosted by the NC State Genetics & Genomics Initiative and the Genomic Sciences Laboratory. See Event Flye<\/a>r<\/a> for more information.<\/p>\n\n\n

<\/div>\n\n\n\n

Illumina DNA Workshop Using the Nextera\u2122 DNA Flex Library Preparation Kit on the NovaSeq 6000<\/h3>\n\n\n\n
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THIS WORKSHOP IS CURRENTLY FULL \u2013 Please email us for inquiries on waitlisting for future workshops.<\/h3>\n\n\n\n

Hosted by the NCSU BIT Program and the Genomic Sciences Laboratory<\/h4>\n\n\n\n

Monday, May 13th (9am-4pm) \u2013 Tuesday, May 14th (9am-12:00pm); Jordan Hall Lab Room 6136<\/h4>\n\n\n\n

Please join us for a hands on experience of our easy and efficient, Nextera DNA Flex Library Prep workflow for WGS of any genome, using your own samples on the GSL NovaSeq 6000. Learn from expert Illumina scientists as they guide you through: Library Preparation & Best Practices, Experimental Design for DNA sequencing Projects, and Data Analysis in BaseSpace\u2122Sequence Hub. Sequencing data will be delivered by the Genomic Sciences Laboratory, followed by a review Q&A session with the Illumina workshop team.<\/p>\n\n\n

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How Hi-C is Transforming Genome and Metagenome Assembly<\/h3>\n\n\n\n
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Thursday, March 28th from 12:00-1:00 PM (Stephens Room \u2013 3503 Thomas Hall).<\/h4>\n\n\n\n

Chromosome conformation capture methods like Hi-C measure the 3D organization of DNA in vivo<\/em> using a combination of crosslinking, proximity-ligation, and paired-end sequencing.<\/p>\n\n\n\n

Because this method captures genomic contiguity on intact chromosomes, the resultant information can be used to generate end-to-end chromosome-scale scaffolds for large genomes.  Since Hi-C junctions form within intact cells, any sequences interacting by Hi-C must have originated from the same species\/strain in a mixed population, enabling metagenomic deconvolution.<\/p>\n\n\n\n