ReadMyCourse for "NGS Data Analysis” | 5 Weeks Program

Greetings from ReadMyCourse!

 

Are you curious about the recent advances in DNA sequencing technology, and how it can be applied to Personalized Cancer Therapy and Disease Research? 

 

So enroll with  ReadMyCourse for "NGS Data Analysis”

You can register this Webinar by using the URL https://bit.ly/3k8UQlx

About Course

NGS has brought a paradigm shift in the field of medicine and agriculture. It enabled us to look into the whole genome of an organism to identify the impact of variants on disease. It became necessary for a biologist to understand NGS technology in order to have a better understanding of disease pathology, diagnosis and suggesting a therapeutic recommendation. The course aims to provide a glimpse of NGS analysis tools with live examples on open-source data.

Course highlights

• A complete NGS analysis training course with open source software, Linux OS, R, and Python.
• NGS data Quality Control – Read QC, Alignment QC, and Variant QC.
• Read mapping, depth, and coverage analysis.
• Short variant identification, variant annotation with RefSeq, dbSNP, 1000 Genome, GenomeAD, and Clinvar.
• Germline and somatic variant calling from whole-exome/clinical exome data and visualization in IGV.
• RNAseq – Differential gene expression analysis, pathway and gene ontology enrichment, PPI network analysis.
• De novo and reference-based genome assembly.
• Metagenomics using QIIME.
• Access to the Linux server to all the students.

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