Trainings and Qualifications

Content: Overview of complete DNA NGS workflows (sample prep, sequencers, and data analysis) with a focus on experimental design and everything that you should consider to be successful in NGS.

Audience: Life scientists who have no or limited experience with NGS, but who would like to gain an understanding of the technology.

Why should you attend: The aim of this course is to give you a practical understanding of lllumina's sequencing workflow to help you with the successful implementation of NGS in your own lab.

Delivery Method: Virtual Class

Duration: ~ 10 h class delivered over 3 sessions

Class Size: Up to 10 participants

Part Number: 20046837

Please note that in order to run this session we need a min. number of 4 participants. In the event the number of confirmed registrations is below the minimum, the class will be cancelled, and you will be offered a place in the next class or have the option to cancel your order.

Your registration will not be confirmed until the payment has been placed.

View complete course schedule and register here

Additional class sessions depend on instructor availability and class interest. If you would like to express interest in attending or have additional questions, please contact us.

Content: Overview of the complete RNA NGS workflow (sample prep, sequencers and data analysis) with a focus on experimental design and everything you should consider to be successful in NGS. During this class we will discuss possible applications of RNA NGS, experimental design considerations, Illumina’s sequencing workflow (including library prep and instrumentation), and data analysis workflow.

Audience: Life scientists who have no or very limited experience with NGS, but who would like to gain an understanding of the technology.

Why should you attend: The aim of this course is to give you a practical understanding of lllumina's sequencing workflow to help you with the successful implementation of NGS in your own lab.

Delivery Method: Virtual Class

Duration: ~ 10 h class delivered over 3 sessions

Class Size: Up to 10 participants

Part Number: 20060629

Please note that in order to run this session we need a min. number of 4 participants. In the event the number of confirmed registrations is below the minimum, the class will be cancelled, and you will be offered a place in the next class or have the option to cancel your order.

View complete course schedule and register here

Content: This course provides an overview of a comprehensive sequencing workflow including comparison of traditional methods used in pathology labs with NGS approach; outline of different NGS strategies, sample preparation methods and sequencing instruments; experimental design considerations for FFPE samples, and introduction to NGS data analysis.

Audience: Pathology lab directors, oncologists and senior clinical scientists who have no or limited experience with NGS, and who would like to introduce NGS into their pathology laboratories.

Why should you attend: The aim of this course is to give pathologists a practical understanding of Illumina’s sequencing workflow to help them with successful implementation of NGS in their own lab.

Delivery Method: Virtual Class

Duration: ~ 10 h class delivered over 3 sessions

Class Size: Up to 10 participants

Part Number: 20060630

Please note that in order to run this session we need a min. number of 4 participants. In the event the number of confirmed registrations is below the minimum, the class will be cancelled, and you will be offered a place in the next class or have the option to cancel your order.

View complete course schedule and register here

Additional class sessions depend on instructor availability and class interest. If you would like to express interest in attending or have additional questions, please contact us.

Content: This course provides an overview of a comprehensive sequencing workflow including a comparison of traditional methods used in microbiology labs vs. NGS approach; outline of different NGS strategies, sample preparation methods and sequencing instruments; experimental design considerations for microbiology samples, and introduction to NGS data analysis.

Audience: Life scientists who have no or limited experience with NGS, but who would like to gain an understanding of the technology.

Why should you attend: The aim of this course is to give microbiologists a practical understanding of Illumina’s sequencing workflow to help them with successful implementation of NGS in their own lab.

Delivery Method: Virtual Class

Duration: ~ 10 h class delivered over 1.5 days

Class Size: Up to 10 participants

Part Number: 20060631

Please note that in order to run this session we need a min. number of 4 participants. In the event the number of confirmed registrations is below the minimum, the class will be cancelled, and you will be offered a place in the next class or have the option to cancel your order.

View complete course schedule and register here

Additional class sessions depend on instructor availability and class interest. If you would like to express interest in attending or have additional questions, please contact us.

Your new instrument is installed, your library is ready and now you have started to produce some sequencing data…but what does it all mean? How could you evaluate the quality of your sequencing data? What data format would you need to start your secondary analysis, and can you manipulate it on order to improve your alignment? What exactly happens during secondary analysis and what are all these mysterious metrics generated during this process? What do they tell you about your sample and your lab processes? How can you find in thousands of variants those few that are important? What are the tools you could use to work with your data? If you would like answers to those questions and learn more about sequencing data analysis on an example of germline DNA analysis workflow, this training is for you!

During this training you will learn:

• Basics of data analysis workflow
• How to evaluate and troubleshoot sequencing data with SAV software
• Practical tips for choosing a solution for data analysis
• How to generate, evaluate and manipulate FASTQ files
• What secondary analysis metrics are produced and how could you use it for quality control of your lab processes
• What happened during tertiary data analysis

All the sessions are highly interactive, contain demos and hands on activities.

Audience

• Researchers that either would like to start to analyze sequencing data or would like to understand better how data are analyzed to improve communication with internal bioinformatics departments
• Bioinformaticians that would like to better understand how sample manipulation could influence data output
• Lab managers who would like to understand how to use sequencing metrics to improve quality control of the lab processes

To truly benefit from the content of this training, basic understanding of the sequencing workflow and NGS data analysis is recommended.

Delivery Method: Virtual Class

Duration: ~ 12 h class delivered over 3 days

Class Size: Up to 10 participants

Part Number: 20060632

Please note that in order to run this session we need a min. number of 4 participants. In the event the number of confirmed registrations is below the minimum, the class will be cancelled, and you will be offered a place in the next class or have the option to cancel your order.

View complete course schedule and register here

Additional class sessions depend on instructor availability and class interest. If you would like to express interest in attending or have additional questions, please contact us.