Sequence Data Analysis

Eureka Genomics' sequence data analysis ability is based on seven years of advanced algorithms and data structures research and development at the University of Houston Bioinformatics Lab. Additionally, Eureka Genomics has an extensive data collection of 500 bacteria, 100,000 viruses, several dozen host genomes including human, 5,000,000 human SNPs and 40,000 human ESTs, that can be used to aid post—sequence analysis.

The Eureka Genomics proprietary algorithms and data structures can be used for sequence data analysis in the following areas:

• Identification of sequencing errors from all types of NGS instruments
• Resequencing and Mapping reads to reference genome(s)
• Identification of microbial/viral genomic variation (SNPs, small insertions and deletions, and gene loss)
• De Novo assembly of genomes
• Detection of foreign genomic material (DNA/RNA) in the presence of host genome
• Custom Projects

Analysis can be performed on sequence data generated from all three commercially available NGS instruments.