Smart Software for Genomic Analysis


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.

Guided demo

Arrange a demo guided by a member of our team.

Schedule guided demo

More information

Have a question about PhenoTips® Genomics Suite?

Request more info

Phenotype-based gene prioritization

Identify disease-causing variants faster with instant gene prioritization based on your patient phenotype.

Gene prioritization
Trio analysis

Pedigree powered trio analysis

Instantaneous filtering for dominant, recessive, or de novo variants.

Cohort filtering based on patient characteristics

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.

Cohorts
Chromosome

Flag and annotate variants as you curate your data

Mark variants that require further validation, look suspicious or are insignificant. Add clinical annotations as you go along for future review.

Speed up your analysis with lightning fast queries

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.

Lightning fast queries
Responsive user interface

Flexible, smooth, and responsive tabular interface

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.

Guided demo

Arrange a demo guided by a member of our team.

Schedule guided demo

More information

Have a question about PhenoTips® Genomics Suite?

Request more info