WORKSHOP / TRAINING
50% Advance is must before starting the training
(30 Days Program for both Online/Offline), Week end batches also available depends on selection
2 Hours / Per Day (As per trainee Convince Time)
50% Advance is must before starting the training
Certificates will be provided at the end of training from Finoseq
Optional: Further Research Support will be provided based on your target studies (Publication Charges is responsible from Trainee)
(Section-I)
Introduction to Bioinformatics
Understanding Genomics Bioinformatics
Databases & tools (NCBI,UCSC,BLAST,BLAT etc)
Understanding of Genomic data
Gene Prediction & Genome Annotation
Genome Vizualization
Basics of Programming (Python) & Linux for NGS data analysis
(Section-II)
Understanding the concept of single guide RNA (sgRNA) & designing sgRNA
Data Retrieval (NCBI SRA) & Introduction to data types
Read Quality Check (FastQC)
Alignment of reads using reference Genome (BWA/Bowtie)
Understanding Mapping Output (SAM/BAM, Samtools & Bedtools)
Variant detection using GATK & Samtools
Visualization of variation with IGV
Complete annotation and variant effect prediction (VEP / SPEff etc)
Understanding and analysis of mutations from CRISPR edited Genome
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