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2026-27 CatalogueRare DiseaseReproductiveH ealthBioinformatics EnterpriseAI & Decision SupportOncology & PharmacogenomicsCardiogenomicsFoensicsLab Management System GENOMICS INTELLIGENCE PLATFORM FROM SAMPLE TO INSIGHT
NEOM Scientific Solutions is dedicated to harnessing genomic intelligence for advancing clinical, research, and forensic applications, ensuring innovative solutions are embedded in every aspect of our operations. Our vision is to to develop innovative, reliable, and cost-effective solutions in genomics and bioinformatics by advancing indigenous research in forensics, molecular diagnostics, genomic kits, and computational biology software platforms that support healthcare, research, and precision medicine. Vision and Mission Core Pillars of NEOM Scientific Solutions Page 2
NEOM SCIENTIFIC merges state-of-the- art technology with expertise, providing a comprehensive approach to forensics and clinical genomics. Our integrated solutions are designed to enhance accuracy and streamline outcomes in both clinical and forensic settings. By leveraging advanced AI and software platform, NEOM SCIENTIFIC promotes innovation made in India while ensuring end-to-end seamless genomics solutions. This empowers researchers and clinicians with vital insights for better decision-making and enhanced patient care. Why NEOM SCIENTIFIC Integrated Solutions for Genomics Excellence Page 3 The Technology Ecosystem unifies Molecular Diagnostics, Bioinformatics, AI, and Clinical Decision Support, creating a comprehensive framework for genomic intelligence. This integration enhances accuracy and efficiency in diagnostics and personalized medicine. By leveraging cutting-edge technologies, NEOM harnesses data-driven insights to streamline workflows and improve patient outcomes. Our approach ensures that genomic solutions are accessible, reliable, and tailored to meet diverse clinical needs.
NeoGI - The Genomics Intelligence Platform From Sample to Insight: A Data Journey Page 4 The Genomics Intelligence Platform architecture illustrates the seamless flow from sample collection to insightful analytics. Each step in the process is meticulously designed to ensure efficiency and accuracy, transforming biological data into valuable insights for clinical and research applications. By integrating state-of-the-art technologies, such as AI, Machine Learning and advanced analytics and computation, the platform enhances decision-making capabilities. This comprehensive approach allows for real-time insights, driving innovations in genomics and enabling healthcare professionals to implement personalized treatment plans effectively.
Page 6 The Clinical Genomics Portfolio at NEOM SCIENTIFIC encompasses cutting-edge solutions lioffering comprehensive genomic testing for various conditions. Our workflows are meticulously designed to ensure accuracy and efficiency in clinical applications, enhancing patient outcomes through innovative technology and expert analysis. Clinical Genomics Portfolio Innovative clinical testing workflows ReproductiveHe alth CardiogenomicsRare Disease Oncology & Pharmacogenomics gDNA Blood Extraction Kit cf DNA Blood Extraction Kit FFPE DNA Extraction Kit NeoBead Purification Kit NeoBCT -cfDNA collection tube Sample Collection Extraction DNA Purification Kit Library Preparation Kit NeoComprehensive Exome Kit NeoClinical Exome Kit NeoCarrier Screening Kit PreView LP WGS Kit PreSight LP GWS Kit NeoMyeloid Kit NeoBRCA Kit NeoComprehensive Onco Kit NeoCardio CMS Kit NeoCardio Comprehensive Kit PreView Compute Lite PreView Compute Pro PreSight CardioPredict CardioSure Computational Solution Page 5 MyeloScan OncoScan Clinexis ATLAS
Rare diseases often stem from genetic mutations, requiring advanced genomic solutions for accurate diagnosis and treatment. Our focus on exome and genome applications aims to unlock critical insights into these conditions. By leveraging cutting-edge technology, NEOM Scientific provides comprehensive genomic analysis to identify rare genetic disorders. This approach enhances patient outcomes through tailored treatment strategies, ensuring a brighter future for affected individuals. Rare Disease Genomics Exome and Genome Applications Explained Page 6 High End- Comprehensive NGS Suite for Genome, Exome, Clinical Exome and Targeted Panel NeoExome : Comprehensive Exome Kit The NeoExome V3 is a high- performance Whole Exome Sequencing (WES) solution designed by Neom Scientific Solutions for targeted sequencing of the human protein-coding genome. Covering target region of ~36.77 Mb with 53.50 Mb probe covered region, it targets > 20,000 genes with exceptional depth and uniformity. Optimized for Illumina platforms, the NeoExome V3 delivers robust detection of SNVs, Indels, and CNVs, ensuring reliable results. Clinexis : Tertiarty Analysis Software Clinexis is a high-performance genomic variant annotation and interpretation platform designed to transform FASTQ or VCF data into structured, phenotype-aware analytical outputs. FASTQ and VCF ingestion Comprehensive variant annotation HPO-integrated phenotype matching Demographic-aware filtering models Variant prioritization frameworks Structured summary and export outputs Batch and cohort-level processing
Reproductive Genomics encompasses innovative solutions like PreView NIPT and carrier screening, aimed at providing expectant parents with critical information about their baby's health and genetic risks. Our prenatal solutions facilitate informed decision-making, ensuring a healthier future for families by detecting potential genetic abnormalities early in pregnancy and providing comprehensive support throughout the process. Reproductive Genomics Empowering Families Through Genetic Insights Page 7 In-House Comprehensive Solution PreView Compute Lite PreView Compute Pro PreView Comprehensive Kit PreView LP WGS NIPT Kit PreSight LP WGS PGS Kit
Reproductive Genomics PREVIEW COMPUTE:IN-HOUSE SOLUTION PreViewCompute is a specialized prenatal genomic analysis platform designed to process raw sequencing data and associated metadata to generate structured, per- sample summary reports for the assessment of potential fetal genetic abnormalities. Engineered for precision, consistency, and ethical compliance, PreViewCompute enables standardized prenatal genomic workflows . PREVIEW cfDNA COMPREHENSIVE KIT: PreView cfDNA System is a comprehensive solution for the genomic labs working in the area of reproductive health, oncology , transplant monitoring, auto immune disorders. PreViewTM is a complete solution for low-pass Whole Genome Sequencing (WGS) of circulating cell-free DNA (cfDNA). Designed for research applications requiring non- invasive genome-wide profiling, PreViewTM provides robust detection of chromosomal aneuploidies, copy number variants (CNVs), and structural alterations using as little as 5–10 ng of input cfDNA. PreSightCompute : IN-HOUSE SOLUTION PreSightCompute is a specialized pipeline execution platform built to streamline Preimplantation Genetic Testing for Aneuploidy (PGT-A) workflows. It processes raw sequencing data, Excel-based metadata, and NDI files to generate structured, reproducible summary sheets for embryo analysis. Preview ScWGA Kit v2 Single-cell Whole Genome Amplification kit optimized for uniform genome coverage from low-input DNA samples. Page 8
Oncology genomics focuses on targeted therapies and precision medicine strategies to improve patient outcomes in cancer treatment through advanced genomic sequencing and analysis. With NeoAmp and NeoHyb chemistry, we strive to transform cancer care by identifying specific genetic mutations that drive cancer, enabling personalized treatment plans tailored to individual patient profiles. OncoScan powered by NeoGI supports end to end comprehensive analysis and reporting. Oncology Genomics Transforming Cancer Care Through Genomics Page 9 Amplicon Technology Hyb Chemistry NeoAmp Universal Chemistry Prepare NGS sequencing library from low input DNA and RNA samples as low as 1 ng to get high quality data. High Multiplexing Capability to amplify 20K+amplicons in a reaction. Ease of use with minimum hands on time. Diverse application with Ready to Use Panels and Made to Order Panels. Hybrid capture technology is a target enrichment method used in next-generation sequencing (NGS) to selectively isolate specific DNA or RNA regions before sequencing. It uses biotin-labeled oligonucleotide probes that hybridize (bind) to complementary target sequences. OncoScan OncoScan is an automated targeted variant detection platform purpose-built for Acute Myeloid Leukemia (AML) analysis. It processes FASTQ data from amplicon- based sequencing workflows to generate high-quality VCF outputs optimized for hematologic variant assessment.
Page 10 Cardiogenomics focuses on the intersection of genetics and cardiovascular health. By understanding genetic markers, we provide tailored insights for prevention and treatment of heart diseases, leading to better patient outcomes. Precision health leverages genomic data to create personalized healthcare solutions. This approach not only enhances diagnostic accuracy but also facilitates targeted therapies, ultimately improving quality of life for patients with cardiovascular conditions. Cardiogenomics Solution Precision Health and Genetic Innovation
CAD Risk ScoreAVERAGE RISKMODERATE RISKHIGH RISK0.60Gene (Transcript) Variant Type Location Zygosity Disease Inheritance Classificatio n TNNI3 (NM_000363 .5) chr19- 55156649-C-T c.29G>A p.(Trp10Ter) Depth: 71x Splice region variant Intron 3 Heterozygou s Cardiomyop athy,familial restrictive, 1 Autosomal Dominant Variant of Uncertain Significance Page 11 NeoComprehensive Cardio Kit: Comprehensive cardiovascular gene panel covering inherited cardiac disorders and cardiomyopathies. Key Features The kit targets genes for Type 2 Diabetes Inherited Bleeding Disorder Obesity Lipid Disorders and Smoking Vasculitis Cardiomyopathy Arotopathies Cardiogenomics Insights Precision Health and Genetic Innovation CardioPredict: Cardio-Predict is an automated cardiovascular genomics reporting system that transforms processed genomic data into structured Coronary Artery Disease (CAD) genetic risk reports in Word and PDF formats. CardioSure: Cardio-Sure is a cardiovascular-focused genomic processing pipeline that converts raw FASTQ sequencing data and metadata into structured, analysis-ready VCF outputs for cardiomyopathy and cardiometabolic syndrome assessment.
Page 12 The NeoTyper Solutions offer cutting- edge technology for forensic analysis, enabling accurate identification through Autosomal STR, Y-STR, X- STR, and mtDNA profiling. These methods are essential for solving complex cases and ensure reliability in criminal investigations. By combining advanced genomic techniques with robust data interpretation, NeoTyper enhances forensic outcomes. Our solutions are designed to meet the highest standards, ensuring that law enforcement officials have the tools necessary for precise and actionable insights in forensic genomics. Forensic Genomics Advanced solutions for criminal investigation and identification
NeoTyper KinStar: NeoTyper KinStar is a software tool designed to evaluate genetic relatedness between individuals using Short Tandem Repeat (STR) marker data. It compares STR allele profiles across multiple loci and calculates statistical measures based on allele sharing and population frequencies. The software provides quantitative metrics to assess biological relationships between samples. STR allele profile comparison across multiple loci Calculation of relatedness metrics based on allele sharing Statistical analysis using population allele frequencies Support for multi-sample relatedness evaluation Generation of quantitative relatedness reports Page 13
Page 14 NeoTyper NeoChime: NeoTyper NeoChime is a software tool for analyzing and quantifying genetic chimerism using Short Tandem Repeat (STR) marker data. It evaluates STR profiles to estimate the relative contribution of different genetic sources within mixed samples. STR profile comparison between reference and test samples Identification of informative STR loci for chimerism analysis Quantification of mixed genetic contributions within samples Automated calculation and reporting of chimerism percentages
Page 15 Neotyper Autosomal STR Kit : The NeoTyper Autosomal STR Kit is a next-generation multiplex PCR system developed for forensic DNA analysis with 23 autosomal STR loci, 3 Y-STRs, Amelogenin, and 1 Y-Indel marker. Neotyper Y STR Kit : NeoTyper YSTR kit is a highly specialized forensic DNA typing solution designed for the amplification of Y-chromosomal short tandem repeats (Y-STRs).Tailored for male- specific identification,the kit is ideal for challenging forensic samples,such as mixtures with high female DNA content or low-template Neotyper X STR Kit : NeoTyperX STR kit is a highly specialized, customizable solution designed exclusively for forensic DNA analysis. Optimized for accuracy and reliability, the kit enables forensic laboratories to perform rapid and precise STR (ShortTandem Repeat)profiling, crucial for human identification, criminal investigations,and paternity testing. Neotyper mtDNA Kit : NeoTyper mtDNA kit is a high performance multiplex SNP genotyping kit designed to enable precise analysis of mitochondrial DNA for forensic,ancestry,and kinship applications.The kit includes reagents optimized for degraded or low-input DNA samples and provides accurate detection of maternal lineage-specific SNPs across key mtDNA regions.
The NeoGI Ecosystem seamlessly integrates diverse components, enhancing genomic intelligence and operational efficiency. By leveraging advanced technologies and AI-driven analytics, the NeoGI Ecosystem empowers healthcare professionals to make informed decisions. This comprehensive framework ensures precision and reliability in genomic diagnostics and research initiatives. NeoGI Enterprise Solution Comprehensive Integration for Genomic Solutions Page 16 NeoGI Enterprise Solution is a comprehensive suite of solution which includes NeoGI Platform, Laboratory Information System-ATLAS and Tertiary Analysis Software Systems: TM (A)NeoGI Platform: A unified suite of advanced solutions tailored for diverse clinical and research genomics needs, enabling precision, scalability, and actionable insights across the healthcare spectrum: TM Converts raw NGS sequencing run data into high-quality FASTQ files. An automated variant analysis that processes FASTQ files to generate reliable VCF outputs through standardized bioinformatics pipelines. High End Core Computational Engine. (B)Tertiary Analysis Platform : ClinexisTM OncoScan TM PREVIEW TM PRESIGHT TM (C)LABRORATY INFORMATICS SYSTEM : ATLAS TM
NEOM Scientific Solutions focuses on collaborative research to advance genomics, ensuring optimal outcomes through partnerships with leading institutions and organizations that share a commitment to innovation and excellence. Our translational genomics efforts bridge the gap between laboratory discoveries and clinical applications, translating genomic insights into actionable solutions that benefit patients and enhance healthcare delivery worldwide. Collaborative Research Advancing Genomics through Partnerships Page 17
Manufacturing Quality Assurance and Compliance Standards Certification Standard Reference Status ISO 13485 Medical Devices IN571425H Compliant ISO 9001 Quality Management 26UQAE30 Compliant ISO 27001 Information Security 26UQAB34 Compliant Startup India Initiative DIPP124404 Registered MSME Small Business UDYAM-UP- 28-0077471 Certified Page 18 ISO 18385 Medical Devices PICL/RHBF/09 23/5241 Compliant GEM-QCI Quality Council of India VA- 419501122186437 Certified
Launch Initiatives Phase 1 Expand Partnerships Phase 2 Enhance Technology Phase 3 Scale Operations Phase 4 Market Integration Phase 6 Research Innovations Phase 5 Page 19 The Strategic Roadmap outlines key initiatives that will drive NEOM Scientific Solutions toward innovative breakthroughs. Each phase represents a critical step in achieving our vision, from launching initiatives to expanding partnerships, and enhancing technology. This roadmap not only serves as a guide for our future direction but also emphasizes our commitment to delivering genomic solutions that meet evolving market needs. Strategic Roadmap Future Vision
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