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Learn more about abm's NGS services at https://www.abmgood.com/Next-Generation-Sequencing-Service.html or email [email protected] to get in touch with our dedicated bio- informatics team.

Today's webinar agenda:
1. Brief overview of next-generation sequencing
2. Understanding NGS data output
3. Whole genome data analysis
4. Working with RNA-Seq data
5. Wrap-up + questions and answers

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New to bioinformatics analysis for NGS data and want to learn more?

One of the benefits of Next Generation Sequencing is the large amount of data that can be generated for each sample and each project. However, it can often be challenging to make sense of your data and perform meaningful analysis to plan the next phases of your research.

For all types of NGS, sequencing is often just the beginning of the project. Once you have this data, you may want to look for small insertions or deletions in your samples (Whole Genome Sequencing), learn about differentially expressed genes after treating your cells with a specific drug (RNA-Seq), or determine which prokaryotes compose the microbial community present in a soil or water sample (16S rDNA Metagenomics).

Searching through large data sets and interpreting your results can often be a bit intimidating.

In this webinar we will discuss data analysis for NGS data, including going through examples for different types of analysis you may want to do for your project!

You will learn about:
•An introduction to processing NGS data
•How that data can be used for different types of analytics, including:
– Variant calling
– Differential gene expression
– and more
•Solving common problems that may arise during analysis

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Links to additional NGS resources:
– Knowledge base and videos: https://www.abmgood.com/marketing/knowledge_base.php
– Next Generation Sequencing Blog Posts: https://info.abmgood.com/blog/topic/next-generation-sequencing
– abm's Next Generation Sequencing services: https://www.abmgood.com/Next-Generation-Sequencing-Service.html

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