More clicks. More friction.
Predefined filters. Fixed workflows.
Adapting the question to the interface.
YOU BRING CONTEXT
GeneUIS® Plus
GeneUIS® Plus
helps you explore it.
A phenotype. A clinical observation. A gene. A variant. A family history.
Or simply, “What am I missing?”
The user remains at the centre.
Questioning, exploring, challenging and deciding.
Ask.
Explore.
Understand.
Decide.
Phenotype?Gene?Variant?Family history?What am I missing?
Explore.
Understand.
Decide.
A NEW PERSPECTIVE ON GENOMICS
Move from questions
to clearer answers.
GeneUIS® Plus brings genomic context into one focused analysis experience.
Powered by SMART-One™ & AI
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Context led
analysisQuestions in plain languageBuilt for genomic teams
FROM RAW DATA TO REAL UNDERSTANDING
One connected journey.
Raw genomic data moves through analysis, context and insight in one genomic analysis environment.
- 01 / INPUT
FASTQ
Raw genomic
data in - 02 / PROCESS
Analysis
Powerful analysis
under the hood - 03 / CONNECT
Context
Genomic context
brings meaning - 04 / EXPLORE
Questions
Ask the
right questions - 05 / UNDERSTAND
Insight
Actionable
insight out
A FAMILIAR START. A DIFFERENT POSSIBILITY.
Beyond predefined filters.
From navigating software to exploring the genome.
Keep the question that matters at the heart
of your analysis.
Fewer clicks. Greater clarity.
Contextual questions. Intelligent guidance.
Asking the question that actually matters.
NEW WAY
SEE GeneUIS® Plus IN ACTION
Watch context shape the analysis.
Press play for a closer look at the GeneUIS® Plus experience.
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THE SHIFT IS SIMPLE
From predefined filters
From predefined filters
to contextual questions.
From click-more to the beginning of click-less.
Our Publications & Articles (Powered by GeneUIS® & SMART-One™)
J Community Genet.
Read
paper
Genetic insights: proband-only exome sequencing in pediatric neurological disorders.
DOI: 10.1007/s12687-026-00870-2Genetic Clinics
Read
paper
Expanding the Prenatal Phenotype and Genotype of 22q11.2 Deletion Syndrome through Genome-wide Chromosomal Microarray Analysis.
DOI: 10.4103/GENC.GENC_1_26J Indian Assoc Pediatr
Surg.
Read
paper
Genetic Markers of Spina Bifida: Enrichment of Pathogenic Variants and Variants of Uncertain Significance.
DOI: 10.4103/jiaps.jiaps_193_24J Biochem Clin Genet.
Read
paper
Bridging metabolomics and genomics: genetic counselling for IEMs.
DOI: 10.24911/JBCGenetics.11-2221J Indian Assoc Pediatr
Surg.
Read
paper
Genetic Markers of Spina Bifida in an Indian Cohort.
DOI: 10.4103/jiaps.jiaps_64_24J Biochem Clin Genet.
Read
paper
G6PD deficiency and parkinsonism - an emerging correlation.
DOI: 10.24911/JBCGenetics.183-1726144134Int J Health Sci Res.
Read
paper