Genome Sequencing Data Analysis
Whole Genome Sequencing (WGS) Data Analysis
Unlock the full potential of your genomic data with our high-quality de novo assembly pipelines.
Overview
Uncover the complete genetic blueprint and identify rare mutations, structural variations, and regulatory elements with our rigorous whole-genome pipelines.
Key Features
- Hybrid assembly (PacBio/Illumina)
- Structural variant calling
- Comprehensive gene annotation
- Structural variant calling
- Comprehensive gene annotation
Demo & Results
We assembled a 3Gb plant genome with a scaffold N50 of over 50Mb.
Frequently Asked Questions
Yes, we can process raw reads directly from Illumina, PacBio, or Oxford Nanopore sequencers.
More Genomics
- Whole Genome Sequencing (WGS) Data Analysis
- Whole Exome Sequencing (WES) Data Analysis
- Antimicrobial Resistance (AMR) & Pathogen Genomics Analysis
- Population Genomics & Genome-Wide Association Studies (GWAS)
- De novo Genome Assembly & Comprehensive Annotation
- Comparative Genomics & Evolutionary Analysis