Powerful Features for Sequence Variation Search & Reporting

The GenomeQuest Sequence Variation Discovery Module extends GenomeQuest’s industry-leading IP sequence search and analysis toolsuite with powerful sequence variation search and reporting features. The module makes variation search both more precise and more efficient by enabling searchers to rapidly screen a large set of results, find specific variants with pinpoint precision, and efficiently prepare a high-level overview of their entire result set. Discover how you can:

• Identify sequences comprising any number of specific or broad variations – by position, region, or combination – or exact match.
• Designate one or multiple sites for specific variations, with one or multiple residues specified as replacements. Insertions and deletions are also identified.
• Retrieve point mutations or study a range containing multiple non-specific replacements by “locking” a specific subsequence while varying other regions.
• Display just the desired variations with userconfigurable graphics.
  
• Create an exportable table of all variations found in a given query/subject pair.