4.7
Registration Fee |
|
In US $ |
$ 109 |
In Indian Rupees |
₹ 10045 |
Next Generation Sequencing (NGS) has fundamentally transformed modern healthcare — enabling clinicians and researchers to sequence entire genomes, transcriptomes, and microbiomes faster and more affordably than ever before. The ability to analyze and interpret this sequencing data is now one of the most critical skills in clinical diagnostics, precision medicine, and biomedical research.
In healthcare, NGS is applied across four major areas: variant analysis for identifying disease-causing mutations in genetic disorders; RNA-Seq for understanding gene expression changes in cancer; metagenomics for characterizing microbial communities in clinical samples; and infectious disease genomics for identifying bacterial, fungal, and viral pathogens — including antibiotic resistance profiling.
This workshop is the only program that delivers hands-on training across all four NGS healthcare applications in a single, structured 4-day course — taught by a clinical expert with direct patient care experience.
16 to 19 March, 2026. Live trainer will take online sessions from 8:30 PM - 10 PM India time +5:30 GMT on Zoom.
Most bioinformatics workshops cover one NGS application. This program covers all four — in a single course, with real clinical datasets, taught by a trainer who has worked with these exact data types in real healthcare settings.
Learn to identify disease-causing variants from Whole Genome, Clinical Exome, and Targeted Gene Panel sequencing data — skills used daily in molecular diagnostics labs.
🔬 Cancer RNA-Seq Analysis- Perform RNA-Seq differential gene expression analysis, Gene Ontology annotation, and data visualization — directly applicable to oncology and translational research.
🦠 Infectious Disease Genomics- Identify bacterial, fungal, and viral pathogens from complex metagenomic samples using 16S rRNA and WGS approaches — a critical skill for clinical microbiology.
🛡️ Antibiotic Resistance Profiling- Identify antibiotic resistance genes from whole genome sequencing data and construct phylogenetic trees — a rapidly growing area in clinical and public health genomics.
A 4-day intensive, 100% hands-on online training program covering the most clinically relevant NGS data analysis workflows — from raw sequencing reads to healthcare-relevant biological interpretations.
⏱️ 60–90 Mins Live Daily- Focused, interactive daily sessions with a live expert trainer on Zoom — real-time instruction and Q&A every day.
💻 Run on Your Own System- Work on your own Windows, Mac, or Linux computer. The trainer guides every installation and setup step from scratch.
🔴 Live Trainer — Not Pre-Recorded- Dr. Bharti — a clinical computational biologist with 18+ years of experience — conducts every session live.
🏥 Real Healthcare Datasets- Analyze actual clinical-grade sequencing data — genetic disease variants, cancer expression data, and pathogen metagenomes.
🎥 Session Recordings Included- Every session is recorded and shared after class via YouTube for unlimited self-paced revision.
🏅 Certificate on Completion- Receive a verified BDG Lifesciences certificate with a unique barcode upon completing all assigned tasks.
Each day covers a distinct, clinically relevant NGS application — building your skills progressively from NGS fundamentals to advanced infectious disease genomics.
01- Introduction to NGS in Healthcare- Foundations & Clinical Applications
02- Variant Analysis in Genetic Diseases- WGS · Clinical Exome · Gene Panels
03- RNA-Seq & Cancer Gene Expression- Differential Expression · Visualization · Ontology
04- Metagenomics & Infectious Disease- Pathogen ID · Resistance Genes · Phylogenetics
Gain hands-on experience with the globally trusted tools and platforms used in clinical genomics laboratories, hospital bioinformatics units, and academic research institutions worldwide..
🌐 Galaxy Webserver- The primary analysis platform for this workshop. Run complete NGS pipelines — variant calling, RNA-Seq, metagenomics — through a browser-based interface with no command-line required.. Primary Analysis Platform
👁️ IGV — Integrative Genomics Viewer- Visualize aligned sequencing reads, variant calls, gene expression data, and genomic features across reference genomes in an interactive, publication-ready viewer..Genome Visualization
🔍 QC & Processing Tools- Assess and improve raw NGS data quality — adapter trimming, quality filtering, and data preprocessing before downstream variant or expression analysis.. Data Quality Control
📊 Variant Calling Pipelines- End-to-end variant calling workflows for WGS, clinical exome, and targeted gene panel data — including SNP/INDEL calling, filtering, and clinical annotation. Variant Analysis
🏷️ RNA-Seq Analysis Tools- Tools for count matrix generation, differential expression analysis, statistical testing, GO enrichment, and high-quality visualization of cancer transcriptomic data. Gene Expression
🦠 Metagenomics & Phylogenetics Tools- 16S rRNA and WGS metagenomics tools for OTU classification, species identification, antibiotic resistance gene detection, and phylogenetic tree construction. Metagenomics / Infectious Disease
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.
You don't just watch — you do. Every step of every session is performed by you on your own computer, guided in real time by a live clinical expert trainer.
Learn clinical genomics from someone who has actually worked in clinical settings — with real patients, real diagnostic challenges, and real OMICS data..
👩🔬 Dr. Bharti occupies a rare professional position: she is simultaneously a clinical expert and a computational biologist — with direct experience handling clinicians, patients, and complex genomic data in real healthcare environments. Over her 18-year career, she has developed deep expertise in Molecular Genetics, Transplant Immunology, and Hemato-oncology, bringing a clinical depth to her bioinformatics teaching that no purely academic trainer can replicate.
Her hands-on clinical background spans CAR-T cell therapy, Mesenchymal stem cell therapy, DC & NK cell therapy, and histocompatibility typing — making her uniquely qualified to teach NGS applications in precisely the healthcare specialties this workshop covers. She has extensive practical experience with multiple OMICS platforms for clinical diagnostics and translational research, and builds strong professional networks between clinicians and computational biologists.
🧬 Molecular Genetics 🫀 Transplant Immunology 🩸 Hemato-oncology 💉 CAR-T Cell Therapy 🔬 OMICS Diagnostics 🧫 Histocompatibility Typing
18+Years Experience
ClinicalPatient-Facing Background
OMICSMulti-Platform Expert
90%+Positive Feedback
From medical students to practicing pathologists, from genomics beginners to experienced researchers — this program delivers healthcare-relevant NGS skills for every level.
🎓 Students & Faculty
🏭 Industry Professionals
🏥 Clinical & Healthcare Professionals
No prior coding or bioinformatics experience required. The workshop is structured to build computational confidence progressively — starting from raw sequencing data fundamentals and building up to complete clinical NGS analysis across all four healthcare application areas.
NGS data analysis expertise in healthcare is no longer optional — it is becoming essential across clinical, research, and industry settings. Here is how this certification directly benefits your specific career path.
Since 2010, BDG Lifesciences has delivered internationally recognized training in bioinformatics, genomics, and computational biology — with a consistent reputation for practical, clinically grounded instruction.
✓ Clinically Grounded Expert Trainer- Dr. Bharti's 18+ years of direct clinical and OMICS diagnostics experience brings real-world healthcare context to every session — far beyond what textbooks or pre-recorded videos offer.
✓ 16+ Years of Global Training Excellence- Established in 2010, BDG Lifesciences has trained 2,000+ participants from 40+ countries with a consistent 4.7/5 participant rating across all programs.
✓ 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. (ACN 608 550 849).
✓ Real Clinical Datasets — Not Toy Examples- Analyze actual healthcare-grade sequencing data — the same types of datasets encountered in real clinical laboratories and research hospitals.
✓ All 4 Healthcare NGS Applications in One Program- No other workshop combines variant analysis, RNA-Seq, metagenomics, and infectious disease genomics in a single structured program — a unique competitive advantage.
✓ Verified Certificate with Unique Barcode- Our digital certificates carry a unique barcode for independent verification — trusted by academic institutions, research centers, and employers worldwide.
One fee for all participants. No hidden charges. Includes live sessions, session recordings, and completion certificate.
Participants in India
₹10045 Indian Rupees — same for all Indian participants | Register Now →
Global (Participants Outside India)
$109 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 NGS Data Analysis in Healthcare workshop.
Do I need prior bioinformatics or coding experience to attend this NGS workshop? No prior coding or bioinformatics experience is required. The workshop uses the Galaxy Webserver — a browser-based platform requiring no command-line skills. The trainer builds your skills from scratch, starting with raw NGS data fundamentals on Day 1 and progressing to advanced metagenomics by Day 4.
What makes this NGS healthcare workshop different from other bioinformatics courses? This is the only workshop that covers all four major NGS healthcare applications — variant analysis (WGS/exome/gene panel), RNA-Seq cancer gene expression, 16S rRNA metagenomics, and infectious disease WGS — in a single 4-day program. Additionally, the trainer Dr. Bharti has direct clinical experience with patients and real diagnostic data, giving the training a depth of healthcare context that purely academic instructors cannot provide.
Is this workshop suitable for pathologists and clinical lab professionals? Yes — this workshop is particularly relevant for pathologists, molecular diagnostics lab scientists, oncologists, infectious disease specialists, and clinical researchers. The curriculum is directly aligned with real clinical NGS applications: variant analysis for genetic disease, RNA-Seq for cancer profiling, and metagenomic pathogen identification from challenging clinical samples.
What specific tools and software will I learn? You will gain hands-on experience with the Galaxy Webserver (primary analysis platform), IGV (Integrative Genomics Viewer for visualization), QC and preprocessing tools, variant calling pipelines, RNA-Seq differential expression tools, 16S rRNA metagenomics tools, and WGS-based pathogen genome assembly and annotation workflows. All tools run on your own computer — Windows, Mac, or Linux.
Will I analyze real human clinical data in this workshop? Yes. The workshop uses real healthcare-relevant sequencing datasets — genetic disease variant data (Day 2), cancer gene expression data (Day 3), and clinical infectious disease metagenome samples (Day 4). These are not simplified toy examples — they are the types of datasets you will encounter in real research and clinical laboratory environments.
Are sessions recorded? What if I miss a day? Yes, all sessions are recorded and shared after class via YouTube using the Gmail ID you register with. If you miss a session for any reason, you can complete all tasks by watching the recording at your own pace — the program is designed to be fully self-paced for revision.
Will I receive a certificate after this NGS workshop? Yes. On successful completion of all tasks assigned by the trainer across the 4 days, you will receive a BDG Lifesciences certificate of completion via email. The certificate carries a unique barcode for independent verification and can be printed, shared on LinkedIn, or added to your academic and professional portfolio.
What is the registration fee and how do I register? The fee is ₹10045 for participants in India and $109 USD for international participants. Click the "Register Now" button, select your correct category, and complete the registration. After payment, check your email for confirmation. The Zoom meeting link will be sent approximately 4 hours before the first session. For queries, email workshops@bdglifesciences.com.
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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