High quality and deep coverage genome resequencing on the illumina Genome Analyzer system, de novo sequencing applications of smaller genomes, making use of paired-end read technology and dedicated software solutions

Advantages of Genome Analysis by illumina Next Generation Sequencing technology

• Small template DNA input amount required – down to 100 ng possible
• Low risk of contamination during amplification step
• Massive output of high quality raw data (1,5 GBp per run for single end reads) at low costs
• High accuracy reading through  DNA regions of challenging base composition (homopolymers, GC or AT rich regions)
• Quick  – data  of high quality and depth can be generated within 1 week when libraries are ready

Our Service Offering:

• Detection of Single Nucleotide Variations from whole genome and targeted resequencing
• Analysis of Copy Number Variations
• De novo sequencing and assembly
• Microarray-based enrichment of selected target regions
• Sample multiplexing
• Bioinformatics:  assembly, mapping to reference genome, variants detection, profiles