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Join the Family 6 waitlist

Get updates on embryo screening using culture fluid, supported by genetic data from both parents. Explore Family 6 niPGT-A and the planned niPGT+ expansion.

Family 6 packages

Planned family package

Family 6 · niPGT-A

$12,000

Both parental genomes + screening of up to six embryos.

  • PGT-A chromosome analysis
  • Parental genetic data for embryo analysis
  • Downloadable genomic files

niPGT+ · Planned expansion

Family 6 · niPGT+

$20,000

Both parental genomes + up to six embryos. Builds on niPGT-A with these planned additions:

  • PGT-SR for a known parental rearrangement
  • PGT-M for a known inherited condition
  • Live Birth Score
  • Couple’s Risk Report

Genomic file downloads are also included in the plan.

Programs are in development. Each feature requires validation and a defined scope before clinical use. A Live Birth Score would be an estimate and cannot guarantee pregnancy or live birth.

Get Family 6 updates

Hear about Family 6 and the planned niPGT+ expansion.

Request Waitlist Updates
Prepare an email inquiry for the BHALESHA team. Fields marked with * are required.

Complete these details to prepare an email. You will review and send it from your own email app.

Please do not include patient information, embryo records, or other sensitive clinical data.

Prefer to email directly? sameer.bhalesha@bhaleshainc.com

Non-Invasive PGT Analysis

One family. Up to six embryos.

Our planned Family 6 package brings parental genetic data and embryo screening into one clinic-directed process. Test scope and availability depend on laboratory validation.

Parental Data for Embryo Analysis
Both Parental Genomes
Genetic inputs supporting the laboratory's embryo analysis workflow
Your Clinic Guides the Process
The reporting laboratory reviews results; your clinic explains them and arranges counseling
Embryo screening and planned additions
PGT-A
Family 6 niPGT-A: analysis for whole-chromosome gains and losses

niPGT+ · Planned expansion

PGT-SR
Chromosome imbalance analysis for a known parental rearrangement
PGT-M
Targeted analysis for a known inherited condition
Live Birth Score
A proposed live-birth likelihood estimate for review with your IVF clinic
Coming with niPGT+
Couple's Risk Report

A couple's risk report is planned as part of niPGT+. The laboratory would review findings from both genetic parents for inherited conditions relevant to family planning and report to your clinic.

Subject to laboratory validation and a defined testing scope. Embryo testing for a specific condition is a separate step.

Downloadable Genomic Files
Available Genomic Files
Access available genomic data and reports, subject to clinic and laboratory policies

Why Choose BHALESHA?

Professional tools designed for clinic-directed genomic analysis

Non-Invasive Workflow

Embryo screening uses culture fluid collected by your IVF clinic, with parental genetic data supporting the analysis.

Structured Analysis

Purpose-built tools organize genomic findings for review by qualified professionals.

Data Access

Access available genomic files and reports in accordance with clinic and laboratory policies.