Service Overview
Analyze Illumina, Nanopore, PacBio, or hybrid sequencing data.
What this service is
Short- and long-read sequencing analysis supports different sequencing platforms and project designs. It can include quality control, mapping, assembly, polishing, variant calling, and genome-level interpretation.
How it helps you
This service helps researchers choose the correct workflow for Illumina short reads, Nanopore/PacBio long reads, or hybrid data. It is useful for genome assembly, variant discovery, microbial genomes, plasmids, and complex genomic regions
What you receive from us
You receive sequencing QC, mapping or assembly statistics, polished outputs when applicable, variant or consensus results, genome interpretation, and clean tables/figures for reporting. Each project is delivered within a maximum of one week. You receive a complete publication-ready scientific report including Materials and Methods, Results, Discussion, References, clear tables, high-quality figures when applicable, and full follow-up until publication, including support with reviewer comments and journal responses.
Service advantages
- Short-read, long-read, or hybrid workflow support
- Assembly, polishing, mapping, or variant analysis
- we perform analysis in max 1-week
- we follow up until publication , any reviews pr questions we can revise and replay
- Useful for microbial and genome projects
- Publication-ready report within one week plus full journal follow-up
- you receive a complete report , material and method . result , discussion and references with publishable resolution figures