Genomics & NGS Data Analysis
Specialized Next-Generation Sequencing data analysis. We turn vast amounts of sequence data into precise genomic insights.
This page details Xenoi Biotech's specialized Next-Generation Sequencing (NGS) data analysis services, including Whole-Genome Sequencing (WGS), Whole-Exome Sequencing (WES), targeted panels, and de novo genome assembly. We process high-throughput sequencing data with precision bioinformatics pipelines to deliver comprehensive variant calling and functional annotations. Research teams can explore our pipeline development services or request a project proposal.
Whole-Genome Sequencing (WGS)
High-precision variant calling (SNPs, Indels, SVs, CNVs) across complete genomes.
Whole-Exome Sequencing (WES)
Deep coverage analysis of coding regions for rare disease and population genomics research.
Targeted Panels
Focused sequencing analysis for research-use targeted panels.
De Novo Assembly
De novo assembly and structural annotation of novel microbial and plant genomes.
Looking for practical learning? Check out our bioinformatics workshops and genomics internships.
Get a Quote for Genomics
Tell us your sequencing specifications and data goals.