ReadMyCourse is Giving you the opportunity to learn “NGS data analysis training – FIVE 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 here ReadMyCourse is Giving you the opportunity to learn

“NGS data analysis training – FIVE weeks program"

You can register this course by using the below URL

https://bit.ly/2Z5TJLG

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.

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.
  
• Access to the Linux server to all the students.

The course aims to provide a glimpse of NGS analysis tools with live examples on open-source data.

Visit www.readmycourse.com  for more details & Information

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