24/07/2026
๐ฆ๐๐ฎ๐ฟ๐๐ถ๐ป๐ด ๐๐๐น๐ ๐ฎ๐ด: ๐๐น๐ผ๐๐ถ๐ป๐ด ๐๐ต๐ฒ ๐๐ฎ๐ฝ ๐๐ฒ๐๐๐ฒ๐ฒ๐ป ๐ฅ๐ฎ๐ ๐ฆ๐ฒ๐พ๐๐ฒ๐ป๐ฐ๐ถ๐ป๐ด ๐ฎ๐ป๐ฑ ๐ฃ๐ฎ๐๐ถ๐ฒ๐ป๐ ๐๐ฎ๐ฟ๐ฒ ๐งฌ
In clinical diagnostic labs and modern cancer research facilities, generating Next-Generation Sequencing (NGS) data is no longer the rate-limiting step. The true challenge begins when the sequencer completes running.
How do you translate millions of raw FASTQ reads into a clear, accurate, and clinically defensible variant report?
This transition requires more than just running standard command-line tools. It demands a deep understanding of quality control, alignment parameters, variant calling nuances, and strict adherence to official ACMG guidelines for variant interpretation.
Our upcoming 4-week online workshop is designed to take you step-by-step through this exact workflow.
๐ก ๐ช๐ต๐ฎ๐ ๐ฌ๐ผ๐ ๐ช๐ถ๐น๐น ๐๐ฎ๐ถ๐ป ๐๐ฟ๐ผ๐บ ๐ง๐ต๐ถ๐ ๐ช๐ผ๐ฟ๐ธ๐๐ต๐ผ๐ฝ:
๐น ๐๐ป๐ฑ-๐๐ผ-๐๐ป๐ฑ ๐๐ป๐ฎ๐น๐๐๐ถ๐: Build confidence working with Gene Panels and Whole Exome Sequencing (WES) data.
๐น ๐ฉ๐ฎ๐ฟ๐ถ๐ฎ๐ป๐ ๐๐ป๐ป๐ผ๐๐ฎ๐๐ถ๐ผ๐ป ๐ฎ๐ป๐ฑ ๐๐ถ๐น๐๐ฒ๐ฟ๐ถ๐ป๐ด: Learn practical techniques to annotate raw variants using key global databases like ClinVar and gnomAD.
๐น ๐๐๐ ๐ ๐๐น๐ฎ๐๐๐ถ๐ณ๐ถ๐ฐ๐ฎ๐๐ถ๐ผ๐ป ๐๐ฟ๐ฎ๐บ๐ฒ๐๐ผ๐ฟ๐ธ: Practice evaluating pathogenicity using standardized clinical guidelines.
๐น ๐๐ฎ๐ป๐ฑ๐-๐ข๐ป ๐๐ฎ๐๐ฒ ๐๐น๐น๐๐๐๐ฟ๐ฎ๐๐ถ๐ผ๐ป๐: Apply your knowledge directly to practical clinical case studies.
๐๏ธ ๐๐๐ฒ๐ป๐ ๐๐ฒ๐ ๐๐ฒ๐๐ฎ๐ถ๐น๐:
๐๐ฎ๐๐ฒ๐: 28 July to 19 August 2026
๐ฆ๐ฐ๐ต๐ฒ๐ฑ๐๐น๐ฒ: Every Tuesday and Wednesday
๐ง๐ถ๐บ๐ฒ: 6:30 PM to 8 PM IST
๐๐ผ๐ฟ๐บ๐ฎ๐: Interactive online live sessions with full access to recordings
Whether you are a researcher aiming to publish robust genomic data, a medical practitioner wanting to better understand NGS reports, or a student stepping into bioinformatics, this workshop offers the practical edge you need.
๐ ๐ฆ๐ฒ๐ฐ๐๐ฟ๐ฒ ๐๐ผ๐๐ฟ ๐ฟ๐ฒ๐ด๐ถ๐๐๐ฟ๐ฎ๐๐ถ๐ผ๐ป ๐ฏ๐ฒ๐ณ๐ผ๐ฟ๐ฒ ๐๐ฒ๐๐๐ถ๐ผ๐ป๐ ๐ฏ๐ฒ๐ด๐ถ๐ป:
https://academy.genespectrum.in/clinngs/