Sequencing Data Analysis Part 2 (Korean): Comprehensive DNA pipeline with BaseSpace Sequence Hub™ and Emedgene™.

This webinar provides an overview of DRAGEN^™ DNA pipeline used in analysis of Illumina sequencing data. We also introduce DRAGEN^™ Germline application on BaseSpace Sequence Hub™ that can be used to improve your data analysis experience. Whether you are new or would just like a refresher, this webinar will give you a robust overview of DRAGEN^™ DNA pipeline and Germline analysis with Illumina Software.

We will discuss:

• DRAGEN^™ DNA pipeline overview
• Key Concepts in Variant analysis such as SNV, CNV, and SV
• Germline analysis on BaseSpace Sequence Hub™
• Highlight variant interpretation with Emedgene™

This discussion is intended as a deep-dive of DRAGEN DNA pipeline with general overview of variant analysis fundamentals

유전체 데이터가 풍부해짐에 따라 대규모 데이터로부터 확장된 유전적 인사이트를 얻는 것이 가능해졌으며, 다양한 분석 플랫폼의 발전을 통해 보다 쉽게 데이터 분석을 접할 수 있게 되었습니다. 이번 웨비나는 유전적 발견의 극대화를 가능케 하는 DRAGEN^™ DNA 파이프라인의 주요 분석 단계들에 대해 살펴보고, Small Variants, Copy Number Variants, Structural Variant와 같은 넓은 범위의 유전적 변이를 검출하는 방법에 대해 소개할 예정입니다. 또한 BaseSpace Sequence Hub의 DRAGEN^™ Germline 어플리케이션을 사용하여 파이프라인 셋팅에 대해 살펴보고, Emedgene을 통해 분석 결과 파일들을 해석하는 방법에 대해 소개할 예정입니다.

Speakers:

Seon Jung Yun Technical Applications Scientist, Illumina Korea Seonjung graduated from Konkuk University in 2014 majoring in Microbial Biotechnology. In the following years, She worked for DNALink and Macrogen as an researcher regarding statistical analysis of microarray, NIPT and cancer genomics.She joined Illumina as a Technical Applications Scientist in 2022, with a strong desire to learn more about the NGS technology. She has since specialized in providing technical support for the instrument and bioinformatics queue.