Comprehensive genomic sequencing with state-of-the-art sequencing technologies and AI-powered data interpretation for clinical and research applications
At BioCogniz, we provide cutting-edge Next-Generation Sequencing (NGS) services that deliver unparalleled accuracy, depth, and speed for your research and clinical applications. Our state-of-the-art sequencing platforms combined with rigorous quality control ensure high-quality data generation across a wide range of genomic applications from whole genome sequencing to specialized microbial and cell-free DNA analysis.
Whether you're investigating genetic diseases, studying complex transcriptomes, exploring microbial communities, or developing precision medicine approaches, our comprehensive NGS services provide the foundation for groundbreaking discoveries.
Complete genomic coverage capturing all coding and non-coding regions, structural variants, and complex genomic rearrangements. Ideal for comprehensive genetic analysis, population genomics, and rare disease discovery.
Cost-effective sequencing focused on protein-coding regions (exons), capturing ~98% of disease-causing mutations. Perfect for clinical diagnostics, rare variant discovery, and Mendelian disease studies.
Comprehensive RNA sequencing including mRNA sequencing for gene expression profiling, transcript discovery, alternative splicing analysis, and non-coding RNA characterization. Unlock functional genomic insights beyond DNA sequence.
Complete bacterial, viral, and fungal genome sequencing for pathogen identification, antimicrobial resistance profiling, strain typing, and evolutionary studies.
Amplicon-based sequencing of the 16S ribosomal RNA gene for taxonomic classification and diversity analysis of bacterial communities. Essential for microbiome research.
Ultra-sensitive sequencing of circulating cell-free DNA from blood plasma for non-invasive prenatal testing (NIPT), liquid biopsy, cancer detection, and minimal residual disease monitoring.
We leverage the most advanced sequencing technologies to match your project requirements:
NovaSeq 6000: Ultra-high throughput for large-scale WGS, WES, and RNA-Seq projects
NextSeq 550: Mid-throughput sequencing for targeted panels and transcriptomics
MiSeq: Small genome sequencing, amplicon sequencing, and targeted resequencing
Sequel IIe: HiFi long-read sequencing for structural variant detection, phasing, and complete genome assembly
Applications: De novo assembly, full-length transcripts, epigenetic profiling
PromethION: Ultra-long reads (>100kb) for complex genome resolution
MinION: Portable real-time sequencing for rapid pathogen identification
Applications: Structural variants, methylation detection, rapid diagnostics
What sets BioCogniz apart is our integration of machine learning algorithms throughout the sequencing workflow:
We provide comprehensive data packages tailored to your needs:
Partner with BioCogniz for state-of-the-art sequencing services backed by expert support
Schedule Consultation Request QuoteA: We support all major platforms including Illumina (NovaSeq, NextSeq, MiSeq), PacBio (Sequel IIe), and Oxford Nanopore (PromethION, MinION). Platform selection depends on your application, read length requirements, and throughput needs.
A: Minimum inputs vary by application: 100ng for WGS/WES, 100ng for RNA-Seq, 10ng for cfDNA. We can work with limited samples, contact us to discuss your specific requirements.
A: Standard turnaround is 2-4 weeks from sample receipt, depending on sequencing depth and project size. Express services (7-10 days) are available for urgent projects.
A: Yes! While this page focuses on sequencing services, we offer comprehensive bioinformatics analysis including alignment, variant calling, differential expression, and pathway analysis. Visit our NGS Data Analysis page for more information.
A: Yes, we sequence DNA and RNA from any organism: human, animal, plant, bacterial, viral, and fungal samples. Custom reference genomes can be used for alignment and annotation.
A: We use bank-grade encryption, HIPAA-compliant storage, and secure data transfer protocols. We can sign Business Associate Agreements (BAAs) for clinical projects. Data retention policies are customizable to your requirements.