Test menu
18 tests for fertility and gynaecology clinics. Order, track and read reports in one clinician portal.
Endometrial microbiome
1 test
Profiling of the endometrial microbiome, designed for low-biomass samples.
| Test | What it looks for | Sample |
|---|---|---|
| BloomMap | Profiles the womb lining’s bacteria with a method built for low-biomass samples. | Endometrial biopsy (Pipelle) |
Embryo testing (PGT)
3 tests
Chromosome screening of embryos before transfer, including for rearrangement carriers.
| Test | What it looks for | Sample |
|---|---|---|
| PGT-A | Screens embryos for the right number of chromosomes before transfer. | Trophectoderm biopsy (day 5-6 blastocyst) |
| PGT-SR | For carriers of chromosome rearrangements; finds the balanced embryos. | Trophectoderm biopsy (+ carrier blood for work-up) |
| Non-invasive PGT-A (niPGT-A) | Chromosome screening from the embryo’s culture fluid, used alongside, not instead of, biopsy PGT-A. | Spent embryo culture medium |
Carrier and reproductive risk
3 tests
Carrier screening for couples, plus selected inherited risk markers.
| Test | What it looks for | Sample |
|---|---|---|
| Expanded Carrier Screening | Checks both partners for recessive conditions they could pass on. | EDTA blood or buccal swab (both partners) |
| KIR-HLA-C | Types maternal KIR and partner HLA-C, an emerging marker studied in implantation failure. | EDTA blood (both partners) |
| Thrombophilias | Factor V Leiden and prothrombin variants, tested in selected cases. | EDTA/citrated blood |
Female factor
2 tests
Genetic testing for female-factor infertility and premature ovarian insufficiency.
| Test | What it looks for | Sample |
|---|---|---|
| Karyotype (female) | Full chromosome check from a blood sample. | Peripheral blood |
| FMR1 / POI | Fragile-X changes linked to early loss of ovarian function. | EDTA blood |
Male factor
4 tests
Genetic and sperm testing for male-factor infertility, including the karyotype, Y-microdeletion and CFTR tests that NICE NG257 recommends for defined groups of men.
| Test | What it looks for | Sample |
|---|---|---|
| Sperm FISH | Counts chromosome errors directly in sperm. | Semen sample |
| Y-microdeletions | Missing pieces of the Y chromosome that affect sperm production. | EDTA blood |
| CFTR / CBAVD | Cystic-fibrosis gene changes linked to blocked or absent sperm ducts. | EDTA blood |
| Karyotype (male) | Full chromosome check from a blood sample. | Peripheral blood |
Prenatal
5 tests
Screening and chromosome testing during pregnancy.
| Test | What it looks for | Sample |
|---|---|---|
| NIPT (cell-free DNA prenatal screening) | Screens for trisomy 21, 18 and 13 from a maternal blood draw. | Maternal blood (early gestation) |
| Fetal Karyotype | Full chromosome analysis of the baby. | Amniotic fluid or chorionic villus sample |
| Array-CGH (microarray) | Detects missing or extra chromosome pieces. | Chorionic villus/amniotic fluid, or blood/products of conception |
| QF-PCR | Rapid check for the most common chromosome conditions. | Amniotic fluid or chorionic villus sample |
| Whole-Exome Sequencing | Deep gene sequencing to find a suspected genetic cause. | EDTA blood (proband ± parental trio) |
In development
Our menu starts with fertility and gynaecology. Tests in the following areas are in development.
- Oncology
- Pharmacogenomics
- Rare disease
- Infectious disease
Not sure which tests fit your clinic?
Tell us about your clinic and the indications you see most, and we will map the menu to them on a short onboarding call.