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 * Home Page
 * ENTERPRISE
   * About Us
   * Career
   * Dictionary of Key Concepts
 * SERVICES
 * PRODUCTS
   * DISTRIBUTION
     * Oxford Nanopore Technologies
     * Nonacus
     * Bento
     * Molzym
   * OUR BRANDS
     * Massive Analyser™
     * MassBiome
     * MobiomX™
     * Mini Analyser™
     * nCOV Analyser™
 * Contact Us
 * * 
   * 

 * Home Page
 * ENTERPRISE
   * About Us
   * Career
   * Dictionary of Key Concepts
 * SERVICES
 * PRODUCTS
   * DISTRIBUTION
     * Oxford Nanopore Technologies
     * Nonacus
     * Bento
     * Molzym
   * OUR BRANDS
     * Massive Analyser™
     * MassBiome
     * MobiomX™
     * Mini Analyser™
     * nCOV Analyser™
 * Contact Us
 * * 
   * 

 * Home Page
 * ENTERPRISE
   * About Us
   * Career
   * Dictionary of Key Concepts
 * SERVICES
 * PRODUCTS
   * DISTRIBUTION
     * Oxford Nanopore Technologies
     * Nonacus
     * Bento
     * Molzym
   * OUR BRANDS
     * Massive Analyser™
     * MassBiome
     * MobiomX™
     * Mini Analyser™
     * nCOV Analyser™
 * Contact Us
 * * 
   * 

 * Home Page
 * ENTERPRISE
   * About Us
   * Career
   * Dictionary of Key Concepts
 * SERVICES
 * PRODUCTS
   * DISTRIBUTION
     * Oxford Nanopore Technologies
     * Nonacus
     * Bento
     * Molzym
   * OUR BRANDS
     * Massive Analyser™
     * MassBiome
     * MobiomX™
     * Mini Analyser™
     * nCOV Analyser™
 * Contact Us
 * * 
   * 

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MASSIVE BIOINFORMATICS


WHO ARE WE?

At Massive Bioinformatics, we are a team of dedicated scientists, software
engineers, and bioinformatics experts who are passionate about utilizing the
power of bioinformatics and biotechnology to improve the quality of life on
earth. We specialize in providing pioneering, high-value-added products and
services that leverage biotechnology and information systems to advance health,
science, and technology.

Our team combines their expertise to offer a range of services, software, and
devices that include next-generation sequencing (NGS), COVID-19 genome analysis,
phylogeny and transmission analysis, and whole genome construction from
metagenomic data and many more.  We provide more accurate results and superior
insights with our long-read technology and analysis softwares.

We take pride in our commitment to excellence and are dedicated to providing the
best possible solutions for our clients. Contact us today to learn how we can
help you advance your research and innovation in biotechnology.

CONTACT



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.




PRIVACY

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.


OXFORD NANOPORE TECHNOLOGIES




MOLZYM




NONACUS




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OXFORD NANOPORE




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DISCOVER ALL OUR SERVICES

At MassiveBioinformatics, 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

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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).

MORE INFO

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


MORE INFO
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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.

MORE INFO

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.

MORE INFO
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RNA SEQUENCING

We offer comprehensive RNA-Seq analyses,  differential gene expression (DEGs),
fusion gene discovery, and variant identification such as  SNVs and Indels.
These evaluations are conducted by skilled bioinformaticians utilizing
cutting-edge technology and top-tier algorithms. Our bioinformatics solution
facilitates both a comprehensive overview and detailed exploration of your RNA
data, highlighting expression patterns through heatmap and Principal Component
Analysis (PCA). Addi tionally, enrichment analyses employing databases like
KEGG, GO, DO, Reactome, and WikiPathways yield valuable insights into the
functional implications of your RNA data.

MORE INFO

COVID19 GENOME ANALYSIS

With our customized pipeline for detection of SARS-CoV-2 based on Oxford
Nanopore sequencing technology which utilizes the benefits of long reads. Our
service aligns the reads to SARS-CoV-2 reference genome, calls variants, and
generates a consensus genome sequence. It then determines lineage, clade and
phylogenetic tree information of the sample using Pangolin and NextClade. All
the information with its data and QC metric files gets summarized in one
extensive html report for easy viewing.

MORE INFO
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Next Generation Sequencing

Oxford Nanopore Technologies




PREPARE

$


SEQUENCE

$


ANALYSE




FEATURED IN SCIENTIFIC PUBLICATION


INCLUDES MORE THAN 2,000 PATENTS AND APPLICATIONS


AMOUNT OF DATA THAT CAN BE RECEIVED AT ONCE WITH 48 FLOWCELLS

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ARE YOU READY TO TAKE YOUR RESEARCH TO THE NEXT LEVEL?


REACH OUT!

From customized bioinformatics analysis and interpretation to our innovative
software tools, we have everything you need to accelerate your research and make
groundbreaking discoveries.

Whether you’re an academic researcher, a pharmaceutical company, or a healthcare
provider, we invite you to explore our full range of services and products
today. Contact us to schedule a meeting with one of our experts and discover how
we can help you achieve your research goals. Together, we can make a difference.

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acknowledge our cookie policy, which helps enhance your browsing experience. We
are devoted to fostering a collaborative and innovative community, and our
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