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Next Generation Sequencing | NGS Test | Henotic Diagnostics
Next Generation Sequencing: Fast & Precise NGS Test
Advanced High-Throughput Genomic Next Generation Sequencing Experts
First of all, Next Generation Sequencing (NGS) represents the pinnacle of modern molecular diagnostics, reading millions of DNA sequences in parallel. Essentially, high-throughput NGS technology profiles single nucleotide variants (SNVs), copy number alterations (CNVs), and gene fusions with 100x to 500x coverage depth. As a result, oncologists and medical geneticists pinpoint actionable mutations for precision medicine and rare disease diagnosis.
Book your Next Generation Sequencing at Henotic Diagnostics for unmatched genomic precision. Furthermore, our accredited diagnostic facility operates 24/7 to provide seamless sample collection.
Next Generation Sequencing Quality Standards & Certifications
First, 5.0 Google Rated
Second, 500x Read Depth
In addition, Clinical Bioinformaticians
Furthermore, NABL Accredited
Also, Targeted Panel & Exome NGS
Moreover, ACMG Variant Guidelines
Finally, ISO Certified
Overview of Next Generation Sequencing (NGS)
To begin with, Next Generation Sequencing (NGS) is an ultra-high-throughput DNA sequencing methodology that has revolutionized clinical genetics and oncology. At the same time, experts at Henotic Diagnostics deploy state-of-the-art NGS platforms to analyze gene panels, exomes, and whole genomes.
What Does Next Generation Sequencing Test Evaluate?
Specifically, NGS evaluates single nucleotide variants (SNVs), small insertions and deletions (indels), copy number variations (CNVs), and gene rearrangement fusions. Consequently, medical geneticists identify disease-causing mutations across broad gene panels. Furthermore, high-depth sequencing detects low-frequency somatic mutations in cancer tissue. As a result, oncologists select targeted therapies with high precision. In fact, to review clinical research standards, consult the NIH Clinical Next Generation Sequencing resource.
Furthermore, comfortable reception lounge ensuring a smooth, welcoming intake for genomic sample registration
What is Next Generation Sequencing?
In general, NGS is a massively parallel sequencing technology that reads millions of short DNA fragments simultaneously. Essentially, unlike traditional Sanger sequencing which processes one DNA strand at a time, NGS chemistry reads entire gene networks in a single instrument run. Specifically, fluorescently labeled nucleotides emit distinct optical signals as DNA polymerase synthesizes complementary strands. Therefore, bioinformatic algorithms align billions of reads against human reference databases to report ACMG-classified variants. Additionally, NGS underpins Whole Exome (WES), Whole Genome (WGS), and NIPT testing.
Additionally, high-throughput NGS sequencers process millions of DNA strands simultaneously with extreme accuracy
What Does Next Generation Sequencing Check?
Overall, NGS provides comprehensive variant detection across diverse clinical medical panels:
Major Clinical Next Generation Sequencing Applications
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Targeted Cancer Panels: First, screens somatic mutations (EGFR, KRAS, BRAF, TP53) in solid tumors to guide targeted oncology therapy.
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Hereditary Cancer Panels: Second, detects germline mutations (BRCA1, BRCA2, Lynch Syndrome genes) for familial cancer risk.
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Neuro-Genetics & Cardiology Panels: In addition, maps genes associated with hereditary cardiomyopathies, muscular dystrophies, and epilepsies.
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Whole Exome & Whole Genome Panels: Finally, sequences coding regions (~20,000 genes) or full 3 billion base pairs for rare disease odysseys.
In addition, bioinformatic software pipelines filter sequence variants against global ClinVar databases
When Is Next Generation Sequencing Test Recommended?
For example, oncologists, neurologists, and clinical geneticists order Next Generation Sequencing for precise clinical indications. In particular, NGS is ordered for cancer patients to identify targetable biomarker mutations for immunotherapy or tyrosine kinase inhibitors. Moreover, it is recommended for pediatric patients presenting with unexplained developmental delays, dysmorphic features, or metabolic crises. In addition, individuals with a strong family history of early-onset hereditary conditions undergo NGS gene panel screening.
Clinical Advantage: NGS vs. Single-Gene Sanger Testing
Why Parallel NGS Outperforms Traditional Single-Gene Testing
Ideally, clinicians choose NGS if multiple candidate genes could explain a patient’s symptoms. In addition, if single-gene Sanger tests are run sequentially, diagnostic costs escalate while wasting precious time. Indeed, NGS tests dozens or hundreds of candidate genes simultaneously in one cost-effective workflow.
Next Generation Sequencing Cost Guide
NGS Genomic Service
Approximate Cost (₹)
Targeted NGS Gene Panel (50-100 Genes)
First, targeted NGS panel pricing is ₹22,500 – ₹28,500.
In addition, Whole Exome NGS costs ₹18,000 – ₹25,000.
Pre & Post-Test Genetic Counseling
Finally, expert genetic consultation fee is ₹1,500 – ₹2,500.
Comparison: Next Generation Sequencing vs. Sanger Sequencing
On one hand, Sanger sequencing processes a single DNA fragment per reaction, whereas Next Generation Sequencing reads millions of DNA fragments in parallel. Consequently, NGS is dramatically faster and cheaper for multi-gene disease panels.
Feature
Next Generation Sequencing (NGS)
Sanger Sequencing
Throughput Capacity
First, sequences millions of DNA fragments concurrently.
However, sequences only 1 target DNA strand at a time.
Multi-Gene Panel Capability
Second, tests 50 to 20,000 genes in a single test run.
In contrast, multi-gene testing is extremely laborious & costly.
Somatic Mutation Sensitivity
In addition, high-depth NGS detects <1% low-frequency variants.
Meanwhile, Sanger requires at least 15-20% mutant allele frequency.
Primary Clinical Use
Finally, ideal for complex genetic panels, exomes, & oncology.
Likewise, ideal for single-gene familial mutation validation.
Frequently Asked Questions
Is a Next Generation Sequencing test painful?▼
However, routine peripheral blood collection involves only a standard needle prick, while genomic sequencing is laboratory-based.
Do I need to fast before Next Generation Sequencing?▼
Because genomic DNA extraction relies on cellular DNA rather than blood sugar, fasting is unnecessary.
How long does the sample collection take?▼
Generally, blood collection takes 5 minutes, while high-throughput sequencing and bioinformatic analysis requires 14 to 21 days.
How long until I receive diagnostic results?▼
Fortunately, detailed ACMG-classified variant reports are delivered within 14 to 21 business days.
What is the cost of Next Generation Sequencing?▼
Overall, a high-precision Next Generation Sequencing test ranges from ₹22,500 to ₹45,000 all-inclusive.
Quick Appointment Booking
Schedule your Next Generation Sequencing with accredited genomic experts.
MBBS, MD (Bioinformatics) · 15+ Years Clinical Experience
Furthermore, your Next Generation Sequencing data is evaluated and reported by senior clinical bioinformaticians and molecular pathologists following ACMG guidelines. Consequently, detailed reports provide treating physicians with definitive evidence for patient care.
Real feedback from patients who completed Next Generation Sequencing with us.
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“Targeted NGS gene testing at Henotic Diagnostics identified the exact EGFR mutation in my father’s lung biopsy. Furthermore, the targeted drug treatment has been remarkably effective.”
– Arvind S.
Verified Patient Review
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“Seamless blood sample collection at home for our hereditary cancer panel. In addition, the genetic counselor explained the ACMG report with immense clarity.”
– Rekha V.
Verified Patient Review
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“Transparent price and NABL accredited accuracy. Dr. Pratibha Patil’s lab provides world-class molecular sequencing.”
You can book your Next Generation Sequencing appointment at our Navi Mumbai center through multiple convenient channels: call us directly at 088793 27184, send a WhatsApp message for instant booking, or use the online booking form on our website. Walk-in appointments are also welcome based on slot availability. We recommend advance booking to ensure zero wait times.
Yes, Henotic Diagnostics Navi Mumbai is empanelled with all major insurance companies and TPAs (Third Party Administrators) including Star Health, ICICI Lombard, New India Assurance, HDFC Ergo, Max Bupa, Bajaj Allianz, and many more. We offer cashless processing for Next Generation Sequencing where applicable. Please carry your insurance card and a valid ID for seamless processing.
At Henotic Diagnostics Navi Mumbai, most Next Generation Sequencing reports are delivered within 2-6 hours for routine tests. Critical and urgent reports are expedited on a priority basis. All reports are delivered digitally via WhatsApp, email, and our secure online patient portal. Hard copies are also available at the center upon request. You will receive an SMS/WhatsApp notification the moment your report is ready.
Henotic Diagnostics Navi Mumbai operates 24 hours a day, 7 days a week, including Sundays and public holidays. This means you can schedule your Next Generation Sequencing at a time that is most convenient for you — early morning, late evening, or even overnight for emergency requirements. Our radiology and pathology departments maintain round-the-clock availability.
Yes, Henotic Diagnostics Navi Mumbai is fully accredited by NABL (National Accreditation Board for Testing and Calibration Laboratories) and ISO 9001:2015 certified. Our radiology equipment also complies with AERB (Atomic Energy Regulatory Board) safety standards. These accreditations ensure that every Next Generation Sequencing performed at our facility meets the highest national and international quality benchmarks for accuracy, safety, and reliability.
