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ISTQB Foundational level crash course [Live + Cheat Sheet + Certificate]
Uncategorized ₹199 Add to cart

Professional training and certification platform focused on IT, Agile, Data Management, and AI-driven skills development.

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Advanced NGS Capstone Project – Internship

Reproducible Analysis, Scientific Reporting and Portfolio Development

End-to-end guided NGS project in your chosen domain
Reproducible environment & workflow design guidance
Full analysis pipeline support, start to finish
Scientific report writing & data visualization coaching
Final presentation & portfolio-ready project repository
Project Completion Certificate
12–16 weeks of weekly 1:1 mentoring (18–24 hrs)

Cancer Genomics

Somatic Variant Analysis and Biological Interpretation

Cancer biology & sequencing strategies (tumor-normal design)
Somatic variant calling & filtering
Manual variant review in IGV
Copy-number & structural variant concepts
Cancer databases (COSMIC, ClinVar, OncoKB, CIViC)
Driver prioritization & mutational signatures
Certificate of Completion
12 live sessions, 1.5 hrs weekly

Microbiome Bioinformatics

16S Amplicon Sequencing and Community Analysis

16S rRNA amplicon sequencing fundamentals
Data processing with QIIME 2 / DADA2 concepts
ASV/OTU generation & taxonomic classification
Alpha and beta diversity analysis
Community composition visualization
Biological interpretation & reporting
Certificate of Completion
10 live sessions, 1.5 hrs weekly

RNA-seq Data Analysis

From Raw Reads to Differential Gene Expression

RNA-seq experimental design & quality control
Splice-aware alignment (STAR / HISAT2)
Gene-level quantification & count matrices
Differential expression analysis in R with DESeq2
PCA, volcano plots & expression heatmaps
Functional enrichment (Gene Ontology, pathway analysis)
Certificate of Completion
10 live sessions, 1.5 hrs weekly

NGS Genomic Analysis

Alignment, BAM Processing and Variant Fundamentals

Reference genomes & read alignment (BWA, Bowtie2)
SAM/BAM processing with SAM tools
Coverage & mapping-quality analysis
Genome browsing & visual review in IGV
Introductory variant calling and VCF interpretation
Certificate of Completion
8 live sessions, 1.5 hrs weekly

NGS Data Preparation

Linux, FASTQ Quality Control and Read Processing

Linux command-line fundamentals & file management
Bash text processing (grep, awk, sed, sort, uniq)
Downloading public sequencing data (SRA / ENA)
FastQC & MultiQC quality assessment
Adapter trimming and read filtering
Reproducible project workflow & scripting
Certificate of Completion
8 live sessions, 1.5 hrs weekly

NGS Foundation

Sequencing Technologies, Data Formats and Quality Concepts

NGS platforms & sequencing technologies (Illumina, Nanopore, PacBio)
Library preparation & sequencing workflow
Core NGS file formats: FASTQ, SAM, BAM, VCF, BED, GFF/GTF
Quality, depth & coverage concepts
Public repositories & metadata (SRA, ENA, GEO)
Certificate of Completion
6 live sessions, 1.5 hrs weekly

Bioinformatics Foundation

Sanger Sequencing, Quality Assessment and Sequence Preparation

Hands-on training with real sequencing datasets
Sanger sequencing fundamentals & chromatogram reading
Phred quality scores and quality-region interpretation
Sequence alignment and consensus building
FASTA formatting and sequence preparation
BLAST analysis and biological interpretation
Certificate of Completion
4 live sessions, 1.5 hrs every Saturday

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