Blog Archives

RNA-Seq Workshop – Library Preparation and Introduction to Data Analysis – August 9th to 11th 2017

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

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RNA-Seq Workshop – Library Preparation and Introduction to Data Analysis – February 8th to 10th 2017

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

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RNA-Seq Workshop – Library Preparation and Introduction to Data Analysis – November 15th to 17th

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,

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RNA-Seq Workshop – Library Preparation and Introduction to Data Analysis – May 10th to 12th

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

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Free RNAseq workshop, January 20th 2016

The Bioinformatics core is hosting a free two hour RNA-seq hour work shop on Januray 20th. Please see:  http://bioinformatics.ucdavis.edu/rnaseq-workshopjan2016/

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First PacBio Workshop – generates long-insert libraries, assembles genomes

The first PacBio Library Prep and SMRT-portal workshop held in April generated plenty of SMRT sequencing libraries with inserts of up to 20 kb. The users learnt about the technical background of PacBio sequencing, common applications, the advantages of long read

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PacBio Library Prep workshop and PacBio SMART-Portal bootcamp courses — April 2015

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

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Oct 20-22, 2014 – Next Gen Sequencing Technology and Sequencing Library Prep Workshop: RNA-seq

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

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Oct 29-30, 2013 – Next Gen Sequencing Technology and Sequencing Library Prep Workshop

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

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Sept. 10-11, 2013 – Next Generation Sequencing Technology and Sample Preparation Workshop

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

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