GAME V1
(Genomic Analysis Made Easy)
"GAME v1 is an automated GUI-based genome analysis suite designed for plant genome assembly and annotation from Illumina sequences. It delivers results including sequence quality assessment and trimming, genome assembly, scaffolding, genome completeness evaluation, repeat masking, and functional annotation."
Cancer Research and Bioinformatics with AI/ML Excellence
" Harmonizing Advanced Technology and Biological Insight - Explore the Future of Cancer Research and Bioinformatics Through the Seamless Integration of Artificial Intelligence and Machine Learning. Redefining Precision in the Pursuit of Lifesaving Solutions "
NGS Bioinformatics Services
" Dive into Genomic Mastery with ArrayGen: Elevating Your Research through State-of-the-Art Bioinformatic Services. Unleash the Power of Next Generation Sequencing (NGS) - Seamlessly Integrating Computational Infrastructure, Unraveling the Genomic Tapestry, and Pioneering Algorithm Development for Precision Insights "
NGS Sequencing Services
"ArrayGen provides NGS Sequencing Contract Research. In accordance with research and publication standards, we offer comprehensive sample analysis, custom data analysis, including transcriptome profiling, miRNASeq, whole genome/exome analysis, real-time dataset processing, industry training, and assistance with publication standards figures/tables"
Microarray Data Analysis
"Unraveling the Tapestry of Life: Your Gateway to Precision in Microarray Data Analysis - Explore, Analyze, and Decode the Genomic Symphony with Our Cutting-Edge Bioinformatics Tools "
Computer Aided Drug Designing
"At ArrayGen we provide complete in-depth CADD services and also client based
complete support for drug discovery programs. Wide array of services like docking,
homology modeling, pharmacophore .."
Industrial Certification Program
" Immerse Yourself in Bioinformatics Excellence: The Bioinformatics Industrial Certificate Program (BICP) offers 6 or 12 months of immersive, hands-on training. Delve into NGS and microarray techniques, master R and Python programming, and gain real-world experience through research projects and industry exposure. Elevate your skills with a blend of theory and practical application "
Indias First Genome Browser
"Pioneering Genomic Exploration: Introducing India's First Genome Browser - ANG, crafted by ArrayGen Technologies. A swift and efficient visualization tool designed with Javafx and Java Swing, ANG is at the forefront of next-generation sequencing data analysis. Platform-independent and user-friendly, it redefines genomics accessibility"
design catalog created by ArrayGen.
This unique microarray catalog coversannotated sequenced genome from Archaea, Bacteria and Eukaryota which are designed for Agilent platform.
The ANG Genome Browser is a visualizationtool, developed by ArrayGen Technologies Pvt. Ltd. This is a fast and an efficient genome browser, built with Javafx and Java swing.
ANG Genome Browser was built for latestnext generation sequencing data analysis.
company with wide array of expertise in Genomics algorithm development , microarray, next generation sequencing (NGS) and Bioinformatics services.
Also, involved in various services in bothindustry and academia.We delivered large number of genomics, NGS and Microarray projects, national as well as international.
ArrayGen has a great expertise in Genomicsand we constantly endeavour to surpass the expectations of our customers.
As a result, we always improvise to enrichtheir experience of owning a better Genomics services.
Reference Based
RNASeq
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Denovo Based
RNASeq
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DNASeq - Variation
Calling
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ChipSeq - DNA-Protein
Binding
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Targeted Metagenomics
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Whole Genome
Metagenome
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DNA
Methylation
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Whole Genome Denovo
Assembly
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Single Cell
RNASeq
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LncRNASeq
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miRNASeq
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ATASeq
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CRISPR Data
Analysis
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Cancer Genomics NGS Data
Analysis
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NGS Automated Pipeline
Development
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NGS Novel Algorithm
Development
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NGS Genomics Database
Development
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Microbiome Data
Analysis
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Whole Exome data
Analysis
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Target Capture data
Analysis
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Transcriptome Assembly
Analysis
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Transcriptome
Annotation
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Variation
Annotation
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SNP/Indel
Analysis
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Somatic and Germline variation
calling
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Copy Number Variation
Analysis
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Custom Scripting and Pipeline
Development
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Somatic CNV
Calling
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Comparative Genomics
Analysis
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Circos Genome
Representation
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TCGA Data
Analysis
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Genome
Annotation
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NGS Clinical Data
Analysis
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Epigenetic Data
Analysis
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NGS Covid Data
Analysis
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Whole Genome Variation
Calling
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Metatranscriptome Data
Analysis
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16S/28S/ITS rRNA
Analysis
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