4.7
Registration Fee |
|
In US $ |
$ 54 |
In Indian Rupees |
₹ 4999 |
Whole Genome Sequencing (WGS) is the comprehensive process of determining the complete DNA sequence of an organism's genome — including all chromosomal DNA and mitochondrial DNA — in a single experiment. Using Next Generation Sequencing (NGS) technology, it generates billions of short DNA reads that are then computationally assembled and analyzed.
WGS is transforming clinical diagnostics, precision medicine, cancer genomics, microbial genomics, and evolutionary biology. The ability to identify SNPs (Single Nucleotide Polymorphisms), INDELs (insertions and deletions), structural variants, and copy number variations from whole genome data is now among the most sought-after skills in life sciences research and the pharmaceutical industry.
This workshop teaches you to go from raw sequencing data to biological interpretation — using the same tools and pipelines used in real-world research and clinical laboratories worldwide.
4 to 7 April, 2026. Live trainer will take online sessions from 8:30 PM - 10 PM India time +5:30 GMT on Zoom.
This workshop walks you through every stage of a real-world WGS analysis workflow — from raw data to biological insight.
Raw FASTQ, Data Quality, Control Alignment / De Novo Assembly, Variant Calling, SNP / INDEL Analysis, Variant Annotation, Effect Prediction, Genome Visualization (IGV), Data Interpretation.
A 4-day intensive online training program covering the complete WGS analysis pipeline — for both animal and human genomes — using real datasets and global-standard bioinformatics tools.
⏱️ 60–90 Mins Live Daily- Each session delivers focused, hands-on instruction with real-time trainer support and live Q&A every day.
🖥️ Work on Your Own System (Laptop/Desktop)- Run real WGS analysis pipelines on your own Windows, Mac, or Linux computer — no cloud subscription required.
🔴 Live Trainer — Not Pre-Recorded- A clinical genomics expert with 18+ years of experience guides every session live on Zoom.
🧬 Real Human & Animal Datasets- Practice on actual sequencing datasets — both animal genomes (alignment/de novo) and human genomes (SNP/INDEL).
🎥 Session Recordings Included- Every session is recorded and shared after class for self-paced revision — revisit any topic as many times as needed.
🏅 Certificate on Completion- Receive a globally recognized BDG Lifesciences certificate with a unique barcode upon completing all tasks.
A comprehensive, structured curriculum covering both the theoretical concepts and hands-on analytical skills of WGS data analysis — from raw reads to biological interpretation.
CORE TOPICS
01- Introduction to WGS & NGS Technology- Fundamentals of next generation sequencing platforms, data types, and WGS workflow overview.
02- Experimental Design & Sequencing Data- Understanding sequencing experiment design, file formats (FASTQ, BAM, VCF), and data organization.
03- Data Quality Control (QC)- Assessing raw sequencing data quality, trimming adapters, and filtering low-quality reads using standard QC tools.
04- Alignment & De Novo Assembly with QC- Reference-based alignment for animal and human genomes; de novo assembly strategies; post-alignment QC and validation.
05- Variant Calling- Identifying genetic variants from aligned reads — SNPs, INDELs, and structural variants using established pipelines.
06- Gene & Variant Annotation- Annotating called variants against genomic databases to assign biological and functional significance.
PRACTICAL APPLICATION & OUTCOMES
P1- Variant Analysis on Galaxy Webserver- Run complete WGS analysis workflows using the Galaxy bioinformatics platform — no command-line required.
P2- SNP & INDEL Variant Analysis- Hands-on identification, filtering, and biological interpretation of SNP and INDEL variants in real datasets.
P3- Variant Effect Prediction- Predicting the functional consequence of variants on gene expression, protein function, and disease relevance.
P4- Genome Visualization Using IGV- Visualizing aligned reads, variants, and genomic features using Integrative Genomics Viewer (IGV).
P5- Genotype Comparison & Interpretation- Comparing genotypes across samples, identifying population-level differences, and drawing biological conclusions.
P6- Data Correlation & Biological Insight- Integrating variant data with functional annotation to derive meaningful, publication-quality biological interpretations.
Get hands-on experience with globally trusted NGS analysis tools and platforms used in research institutions, clinical genomics labs, and biotech companies worldwide.
🌐 Galaxy Webserver- An open-source bioinformatics platform for building and running complete WGS analysis workflows. No command-line expertise needed — browser-based and beginner-friendly. Primary Analysis Platform
👁️ IGV — Integrative Genomics Viewer- A high-performance, interactive genomics visualization tool for exploring aligned reads, variant calls, and gene annotations across human and animal genomes.Genome Visualization
🔍 QC & Trimming Tools- Industry-standard tools for assessing raw sequencing data quality, identifying adapter contamination, and filtering low-quality reads before analysis. Data Quality Control
🧩 Alignment & Assembly Tools- Reference-based alignment tools for mapping sequencing reads to known genomes, and de novo assembly tools for organisms without a reference genome. Sequence Mapping
📊 Variant Calling Pipelines- End-to-end variant calling workflows for identifying SNPs, INDELs, and structural variants from aligned whole genome sequencing data. SNP / INDEL Detection
🏷️ Variant Annotation Databases- Tools and databases for annotating called variants with gene function, disease associations, population frequency, and predicted functional effect. Functional Annotation
System Requirement: Any OS — Windows, Mac (macOS), or Ubuntu/Linux — with an internet connection. The trainer guides installation of all required tools from scratch during the sessions.
By the end of this 4-day WGS analysis workshop, you will be able to independently perform a complete genome sequencing data analysis pipeline — from start to finish.
🧬 Run End-to-End WGS Pipelines- Independently execute the full WGS analysis workflow — QC, alignment, variant calling, and annotation — on your own computer.
🔬 Analyze Human & Animal Genomes- Work confidently with both human genome (SNP/INDEL) and animal genome (alignment/de novo assembly) datasets.
📈 Interpret Variant Data Biologically- Translate raw variant calls into meaningful biological insights — genotype differences, disease associations, and functional effects.
🖼️ Create Publication-Quality Visualizations- Generate IGV-based genome visualization figures and analysis outputs suitable for research papers and project reports.
💼 Apply Skills in Research & Industry- Bring real, hands-on WGS analysis competency to your academic research, PhD work, clinical lab, or biotech/pharma career.
🏅 Earn a Verified Certificate- Receive a BDG Lifesciences certificate with a unique barcode — a credible, verifiable addition to your professional profile.
Every session is designed to be practical — you run the analysis yourself in real time, guided step by step by a live expert trainer.
Learn from a clinical computational biologist with 18+ years of professional experience spanning molecular genetics, clinical diagnostics, and OMICS data analysis.
👩🔬 Dr. Bharti is a biologist by degree, a computational biologist by training and passion, and a scientific leader by role. Over an 18-year professional career, she has developed deep expertise spanning Molecular Genetics, Transplant Immunology, Hemato-oncology, and Cellular Therapies — including CAR-T cell therapy, Mesenchymal stem cell therapy, and DC & NK cell therapy — as well as histocompatibility typing.
What makes Dr. Bharti's teaching uniquely valuable is her dual expertise at the intersection of clinical biology and computational genomics. She has extensive hands-on experience with various OMICS platforms for both clinical diagnostics and research applications — a perspective very few bioinformatics trainers in the world can bring to a workshop. She builds strong professional networks, works directly with clinicians and patients, and brings real-world genomics complexity into every training session.
18+ Years of Experience
OMICS Multi-Platform Expert
Clinical Real-World Background
90%+ Positive Feedback
Whether you are a student, clinician, researcher, or industry scientist — this program delivers WGS analysis skills relevant to your field.
🎓 Students & Faculty
🏭 Industry Professionals
🏥 Clinical & Medical Professionals
No prior experience in WGS or bioinformatics required. This program is structured to build your skills progressively — starting from the basics of sequencing data and building up to confident, independent variant analysis.
Whole Genome Sequencing is at the heart of the global genomics revolution. Professionals who can analyze and interpret WGS data are in exceptional demand across research, clinical, and industry settings.
Clinical Genomics & Precision Medicine- WGS-trained professionals are increasingly essential in clinical labs performing genomic diagnostics, rare disease identification, and personalized treatment planning.
Cancer Genomics Research- Somatic mutation calling, tumor genome analysis, and cancer biomarker discovery all rely on WGS analysis skills — a high-growth area in both academia and pharma.
Molecular Diagnostics Labs- Next-generation sequencing is now standard in molecular pathology labs. Pathologists and lab scientists with NGS data skills are highly valued in diagnostics settings.
Pharmaceutical & Biotech R&D- Drug target discovery, pharmacogenomics, and clinical trial design increasingly depend on WGS data. This training directly supports roles in biotech and pharmaceutical R&D.
Academic Research & PhD Programs- WGS analysis is a core skill in modern biology research. This certificate strengthens your PhD applications, research proposals, and publication-quality data analysis.
Bioinformatics & Data Science Roles- The genomics data science sector is growing rapidly. Bioinformaticians proficient in WGS pipelines, Galaxy, and IGV are among the most employable professionals in life sciences.
Since 2010, BDG Lifesciences has trained thousands of students, researchers, and professionals in bioinformatics, genomics, and computational biology — with a globally recognized reputation for practical, research-quality training.
✓ Clinically Grounded Expert Trainer- Dr. Bharti brings 18+ years of real clinical and computational biology experience to every session — a perspective no textbook or pre-recorded video can replicate.
✓ 16+ Years of Global Training Experience- Established in 2010, BDG Lifesciences has successfully trained participants from 40+ countries with consistent 4.7/5 ratings.
✓ Government Registered & Internationally Authorized- MSME-registered under the Govt. of India and officially authorized to operate in Australia & New Zealand via BBR Group Pty Ltd.
✓ Real Datasets — Not Toy Examples- You analyze actual human and animal genome sequencing data — the same type of data you will encounter in real research and clinical environments.
✓ Live + Recorded: Best of Both Worlds- Attend live for expert interaction and error resolution. Access recordings for self-paced revision. You never miss a concept.
✓ Verified Certificate with Unique Barcode- Our digital certificates carry a unique barcode for independent verification — trusted by academic institutions and employers worldwide.
One fee for all participants. No hidden charges. Includes live sessions, session recordings, and completion certificate.
Participants in India
₹4,999 Indian Rupees — same for all Indian participants | Register Now →
Global (Participants Outside India)
$54 US Dollars — same for all international participants | Register Now →
Registration is non-refundable and non-transferable. Please read the full T&C below before registering.
Everything you need to know before registering for this Whole Genome Sequencing analysis workshop.
Do I need prior experience in bioinformatics or WGS to join this workshop? No prior experience in bioinformatics, NGS, or WGS is required. The workshop is structured to build your skills progressively from scratch — starting with the basics of sequencing data and building up to complete variant analysis and interpretation. All installation and setup is covered during the sessions.
What software and tools will I learn in this WGS analysis workshop? You will get hands-on experience with the Galaxy Webserver for running complete WGS analysis workflows, IGV (Integrative Genomics Viewer) for genome visualization, and various QC, alignment, variant calling, and annotation tools. All tools are installed and run on your own computer during the sessions.
What operating system do I need? Can I use Windows or Mac? Any operating system works — Windows, Mac (macOS), or Ubuntu/Linux. All you need is your personal computer or laptop with a stable internet connection. The trainer will guide you through installation and setup from the very first session.
Will I analyze both human and animal genomes in this workshop? Yes. The workshop covers both animal genome analysis (alignment-based and de novo assembly approaches) and human genome analysis (SNP and INDEL variant calling and interpretation). You will work with real sequencing datasets for both.
Are the sessions recorded? What if I miss a session? Yes, all sessions are recorded and shared with you after class via YouTube (using the Gmail ID you register with). If you miss a session, you can still complete the corresponding practical tasks by watching the recording at your own pace.
Will I receive a certificate after completing the WGS workshop? Yes. Upon successfully completing all tasks assigned by the trainer, you will receive a BDG Lifesciences certificate of completion via email. The certificate includes a unique barcode for independent verification and can be printed or added to your LinkedIn profile.
What is the registration fee for the WGS online workshop? The fee is ₹4,999 for participants in India and $54 USD for participants outside India. The fee is the same for all participants within each category — students, researchers, and professionals alike. Registration is non-refundable and non-transferable.
Is this WGS workshop useful for pathologists and clinical lab professionals? Absolutely. This workshop is particularly valuable for pathologists, molecular diagnostics lab scientists, and clinical researchers because the trainer Dr. Bharti has direct clinical experience herself. The curriculum includes clinically relevant applications like variant effect prediction and disease-relevant genome interpretation.
How do I register for the BDG Lifesciences WGS Workshop? Click the "Register Now" button on this page. Select your correct participant category (India or outside India), complete the registration form, and proceed to payment. After registration, check your confirmation email for next steps. For queries, email workshops@bdglifesciences.com or chat with our AI Assistant George on the website.
Secure your spot in 3 simple steps — seats are limited for each batch.
1️⃣ Click Register Now- Click the Register Now button and select number of tickets you want to buy..
2️⃣ Check Your Confirmation Email- After successful payment, check your email for a confirmation with registration details and next steps.
3️⃣ Receive Your Zoom Link- Once registration closes, you'll receive the Zoom meeting link and be added to the workshop WhatsApp group.
📧 Need help? Email us at workshops@bdglifesciences.com or chat with our AI Assistant George at bdglifesciences.com
BDG LifeSciences is a distinguished bioinformatics company established in 2010 and operates globally. Headquartered in India, the company specializes in facilitating workshops, training programs, novel and innovative research projects, and online courses in bioinformatics and life sciences. BDG LifeSciences is registered under the Ministry of MSME (Micro, Small, and Medium Enterprises), Government of India, with the registration number UDYAM-UP-01-0019151. In January 2024, BDG LifeSciences, India, has authorized BBR Group Pty Ltd., Australia (ACN 608 550 849), to operate its programs in Australia and New Zealand.
With a strong focus on the practical application of technology, BDG LifeSciences provides hands-on training where participants work on their own computers/laptops using specialized software and servers. The company has been a leader in this sector for the last 16 years, successfully educating a diverse range of participants, including students, scientists, faculty members, professors, and corporate executives worldwide.
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