PhenoTips® Genomics Suite contains a high-performance genomic variant database that enables clinicians and researchers to quickly and easily analyze next-generation sequencing (NGS) results at very large scale.
Unlock the full potential of your phenotypic and genomic data to achieve a precise diagnosis, more easily than ever.
Instantaneous filtering for dominant, recessive, or de novo variants.
Dynamically create cohorts based on structured patient data and filter against patients in your entire institution. Compare allele frequencies in your cohorts with background population.
Mark variants that require further validation, look suspicious or are insignificant. Add clinical annotations as you go along for future review.
Query and sort on multiple columns simultaneously with variants returned in less than 1 second. With X patient exomes, a query for " ... " is returned in Y seconds. For X patient genomes, it takes Z seconds.
Scrap the spreadsheets and access all your patient genomes and exomes in one central place. No need to switch between multiple spreadsheets to analyze your patients' genetic data.