2nd Illumina Hands-On DNA Re-Sequencing Workshop on July 25th
Since the July 24th workshop was fully booked immediately, we are offering an additional workshop on the following day. Please join us for a hands-on workshop on DNA sequencing library preparation and data analysis using the Nextera DNA Flex library prep kit (focusing on re-sequencing).
Illumina Hands-On DNA Re-Sequencing Workshop on July 24th
Please join us for a hands-on workshop on DNA sequencing library preparation and data analysis using the Nextera DNA Flex library prep kit (focusing on re-sequencing).
August 9th, 9 a.m. – August 11th, 5 p.m.
RNA-seq has revolutionized the way we address complex biological questions, allowing for differential gene expression, differential transcript analysis, as well as transcriptome assemblies. As sequencing output rapidly increases and sample numbers increase, library preparation becomes one of the major bottlenecks. This workshop provides comprehensive hands-on training in the preparation of high quality RNA-Seq libraries for the Illumina platform.
February 8th, 9 a.m. – February 10th, 5 p.m.
RNA-seq has revolutionized the way we address complex biological questions, allowing for differential gene expression, differential transcript analysis, as well as transcriptome assemblies. As sequencing output rapidly increases and sample numbers increase, library preparation becomes one of the major bottlenecks. This workshop provides comprehensive hands-on training in the preparation of high quality RNA-Seq libraries for the Illumina platform.
We are sorry the workshop is fully booked.
To subscribe to the our email list which announces the workshops, send an email to sympa@ucdavis.edu with the following information in the subject line:
subscribe dnatech_news first_name last_name
November 15, 2016, 9 a.m. – November 17, 9 a.m. to 6 p.m.
RNA-seq has revolutionized the way we address complex biological questions, allowing for differential gene expression, differential transcript analysis, as well as transcriptome assemblies.
May 10, 2016, 9 a.m. - May 12, 2016, 9 a.m. to 6 p.m.
Please see this page for the full information and the registration:
https://registration.genomecenter.ucdavis.edu/events/DNATech_RNASeq_May_2016/
RNA-seq has revolutionized the way we address complex biological questions, allowing for differential gene expression, differential transcript analysis, as well as transcriptome assemblies.
UC Davis Genome Center Workshop on PacBio Sequencing and Data Analysis (Wet lab and Bioinformatics)
PacBio sequencing is the method of choice for de novo assembly of high quality genome sequences (see these AGBT presentations), the sequencing of long amplicons and complex repetitive regions, the analysis of gene isoforms, and structural variant detection.
Next Generation Sequencing (NGS) has revolutionized the way that we address complex biological questions. As sequencing output rapidly increases and experimental scales get bigger, library preparation becomes one of the major bottlenecks for NGS. This course provides a comprehensive hands-on training on how to prepare high quality libraries for Illumina HiSeq2500 and MiSeq sequencing platforms. Participants are encouraged to bring their own total RNA template and, by the end of the course, will have a library ready for NGS sequencing.
Next Generation Sequencing (NGS) has revolutionized the way that we address complex biological questions. As sequencing output rapidly increases and experimental scales get bigger, library preparation becomes one of the major bottlenecks for NGS. This course provides a comprehensive hands-on training on how to prepare high quality libraries for Illumina HiSeq2500 and MiSeq sequencing platforms. Participants are encouraged to bring their own total RNA template and, by the end of the course, will have a library ready for NGS sequencing.
Next generation sequencing (NGS) technologies allow laboratories to do genome-wide research that was previously only possible at large genome centers. Participants will learn key concepts and applications of major sequencing technologies (Illumina, 454, SOLiD, Ion Torrent & PacBio) including technology basics, technology-specific error modes, experiment design considerations, common data analysis workflows (like RNA-Seq, genome assembly, ChIP-Seq, SNP- and other variant discovery, etc.) and associated IT concerns.
