NextGen Sequence Analysis
This hands-on training will equip participants with knowledge and skills on how to generate, manipulate, and analyze whole genome, whole exome, and targeted NGS data and discover germline SNPs, indels, SVs, and CNVs; somatic SNVs, SVs, and indels, and RNASeq SNPs and indels. The objective is to enhance the researchers‘ capacity to conduct world class scientific research and boost their institution‘s profile as a leading diagnostic and scientific centre.
The training is ideal for graduates in biological, medical, or agricultural sciences who are using or intend to use nextgen sequencing in their work. The training will teach you how to:
- Learn the science, methods and applications of NGS.
- Discover SNPs, SNVs, SVs, indels and CNVs from large genetic datasets
- Identify varinats of clinical significance and diagnose medical conditions.
- Optimize therapy and precision medicine
Dates: Every second and third weeks of the month |
Duration: 10 days. |
Venue: Nairobi, Kenya. |
PREREQUISITES |
This practical training is ideal for graduates in biological, medical, or agricultural sciences who are using or intend to use nextgen sequencing in their work. |
FEES |
Terms and conditions of Payments: |
REGISTRATION |
To register, please download the booking form fill it and send it to us through: Email: [email protected]. |
TOOLS AND SOFTWARE |
SRA Tools, GATK, Picard, IGV, Bowtie-2, BBMap, FastQC, R, Biolinux, Oracle VirtualBox, Sam Tools, Velvet, IGV, NCBI Tools, HapMap, PLINK, SKAT-O, Broad Institute Resource Bundle, KENCLUST, 1,000 Genomes Project, The Cancer Genome Atlas (TCGA). |
Course material including a comprehensive training manual and a CD with software |
TRAINING PROGRAM |
1. Installing and running Biolinux on Oracle Virtual Box 2. Biolinux commandline 3. Short read quality control 4. Introduction to the SRA 5. Understanding the fastq, SAM, and BAM formats 6. File conversion using Sam Tools and SRA tools 7. Reference mapping assembly using BBMap 8. Variant calling 9. De novo assembly using Velvet 10. Rna seq mapping and assembly 11. Phylogeny-based methods for analysis of genomes and metagenomes 12. Genome comparison and phylogeny 13. Exercises 14. Award of certificates |