- Introduction to Bioinformatics
- Linux basics
- R programming basics
- Experimental setup (Basic of wetlab principle of each sequencing methods )
- Basic of NGS data analysis
- NGS for genomics; assembly, alignment, QC and variant calling tools
- NGS read-to-reference alignment (genomic and RNA-Seq)
- Variant calling in populations
- NGS for transcriptomics; QC, mapping, visualisation tools
- Reference of RNA-sequence data
- Statistics used for RNA seq data analysis
- Principle of some MLA like PCA , heatmap , hirarchial clustering
- Functional annotation
- Pathways analysis
- Network analysis
Important Notes:
- Training Mode: Online
- Trainers : Highly Experienced Industry Professionals.
- More interactive class
- Training participation E-Certificate will be provided at the end of the training.
- Queries/support even after training will be encouraged through forum.
- Please feel free to ask if any further information required.
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