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 With Us

Unleash the Power of Genomics: Massive Analyser™

Discover the World Inside You MassBiome™

Unrivaled Efficiency, Unbeatable Value:

Analysis of Anything
by anyone, anywhere

Who are we?

At Massive Bioinformatics, we’re a team of dedicated scientists, software engineers, and bioinformatics experts passionate about using bioinformatics and biotechnology to enhance the quality of life. We provide innovative, high-value products and services that advance health, science, and technology.

Holistic Approach

Our team of software engineers and bioinformatics experts create sophisticated information systems that provide actionable insights and analysis.

Innovative Solutions

We leverage the latest biotechnology to develop groundbreaking solutions that solve real-world problems. Partnerships bring us together.


We understand that genetic information is highly sensitive and can reveal personal and intimate details about individuals. Therefore, we prioritize the privacy and security of genetic data throughout our analysis process. We follow all relevant regulations and standards, including the GDPR and KVKK.

Contact us now!

From customized bioinformatics analysis to innovative software tools, and Next Genereation Sequencing devices we provide everything you need to accelerate your research. Explore our services and products today. Contact us to schedule a meeting with our experts and achieve your research goals. Together, we can make a difference. 

Expert Consultancy

When you contact us, you can discover the most suitable solutions for your projects through one-to-one meetings with our expert consultants.

Customized Services

With services and products tailored specifically to your needs, we will accelerate your research processes and help you achieve your goals in less time.

Oxford Nanopore Technologies

Through the vision of “the analysis of anything, by anyone, anywhere” Oxford Nanopore Technologies (ONT) put forth a new generation of sensing technology. 














Molzym offers ultra-clean, highly active amplification reagents and kits for microbial nucleic acid extraction. Their products are guaranteed to be free of contaminating microbial nucleic acids.













Bento Lab

Bentolab is a portable biotechnology laboratory. It offers the possibility to perform DNA analysis, protein studies and other biotechnological processes in the field or in the laboratory. Ideal for education, research and industry.













Discover all our services

At Massive Bioinformatics, we provide comprehensive bioinformatics solutions to support your scientific research and data analysis needs. From genetic data analysis to bioinformatics consulting, we offer a world of knowledge you want to discover. We invite you to explore our tailored solutions and unlock your research potential!

Antimicrobial Resistance

Antimicrobial resistance (AMR) is a critical global health issue addressed through metagenomics, which examines resistomes in diverse microbial environments. Using Oxford Nanopore’s long reads, antibiotic resistance genes are identified in raw data through shotgun metagenomic and whole genome sequencing, leveraging the Comprehensive Antibiotic Resistance Database (CARD).

16S – 23S Metagenomics

Metagenomics enables the assessment of microbial diversity and quantities within samples. While 16S rRNA gene identification at ~1500 bp is common, many modern sequencing methods use only a ~450 bp fragment, leading to inaccuracies. Oxford Nanopore’s long reading technology enhances species identification by reading the full 1500 bp gene, advancing the field. Metagenomic analyses offer extensive options for detailed exploration of diverse sample types or components.

Whole Genome Sequencing

Whole genome analysis involves a thorough study of an organism’s entire genome and its functional genes. This method detects variants – differences from the reference genome – along with antimicrobial resistance genes, secondary metabolite genes, and virulence genes in the annotated genome. It also includes tools like alignment images, circular genome depictions, genome comparison with close subspecies, polymorphism tables.

Amplicon Sequencing

Experience our Amplicon Sequencing Service—a tailored genetic analysis solution crafted to reveal precise insights from DNA or RNA samples. Through targeted amplification and sequencing of specific regions, we deliver focused, high-resolution data ideal for identifying mutations, uncovering genetic diversity, and tracing variations. Our state-of-the-art technology ensures precise outcomes, even with limited genetic material, enabling swift and cost-effective decision-making. Whether in medical advances or environmental exploration, our Amplicon Sequencing Service paves the way for efficient and impactful genetic analysis.

Next Generation Sequencing

Oxford Nanopore Technologies






Featured in scientific publication

includes more than 2,000 patents and applications

amount of data that can be received at once with 48 flowcells

Our Blog Posts

Welcome to our Massive Bioinformatics Blog! You are in the right place to learn about the latest developments, innovative projects and in-depth analysis in the world of bioinformatics.

Databases that we use in pipelines

Clinical Genomic Database (CGD) Clinical Genomic Database (CGD), is a manually curated database of conditions with known genetic causes, focusing on medically necessary genetic data with available interventions. All conditions with identified genetic causes are...

External Links for Variants

External links can be used as valuable tools to pass through between different useful sources. Different sources links are utilized as external links in this application. These are: VarSome [1] Franklin [2] ClinVar [3] dbSNP [4] HGNC [5]...

Compatible sequencers with Massive Analyser

Sequencing machines are scientific devices that aid in the automation of the DNA sequencing process. In sequencing technology, there are various types of sequencing devices. Each device has its own DNA sequencing methods. Our system currently supports two sequencing...

Compatible Kits with Massive Analyser

Our system supports the kits listed below: 1. Twist 1.1. Twist Comprehensive Exome Panel [1] Exome sequencing has become a widely used practice in clinics and diagnostics. To meet this need, the content of the Twist Human Nucleus Exome has been designed to cover...

Family Trio Analysis

NGS technology of family trio analysis offers a powerful approach for identifying causal variations for inherited diseases. Trio analysis can identify variants inherited from the parents. For example, if a variant appears only in the mother, and the father and child...

ACMG Rules

In 2013, ACMG group members came together to develop a recommendation for using standard terminology for classifying variants using applicable rules. Different rules/criteria are assigned to classify variants bearing the said rule's feature. As mentioned below, each...


Scientific Dictionary Scientific Dictionary A B C D E F G H I M Q S T A Adapter Adapter is an oligonucleotide sequence that is attached to the ends of the DNA sequence by ligation or rapid chemistry. It carries a motor protein that plays a role in separating the...

Dictionary of Key Concepts

    TERM DEFINITION Adapter Adapter is an oligonucleotide sequence that is attached to the ends of the DNA sequence by ligation or rapid chemistry. It carries a motor protein that plays a role in separating the strands of the DNA molecule, aiding the strand...