Sequence 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.
- 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.
Eureka Genomics Corporation: 410 Pierce Street, Ste. 307, Houston, TX 77002 | 750 Alfred Nobel Drive, Hercules, CA 94547
Phone: (510) 964-0461 | Fax: (510) 964-9705 | Email: contact@eurekagenomics.com