One channel. The full fertility-genetics menu.

Every genomic and microbiome test your patients need, ordered through a single BioBloom login.

Endometrial and Microbiome

1 test

Our signature test, developed in Cambridge.

Signature test

Endometrial Microbiome Analysis

Checks the womb lining’s bacterial balance, which is associated with implantation outcomes.

Embryo Testing (PGT)

4 tests

Screening embryos before transfer.

PGT-A

Screens embryos for the right number of chromosomes before transfer.

PGT-SR

For carriers of chromosome rearrangements; finds the balanced embryos.

PGT-M

Tests embryos for a specific inherited disease that runs in the family.

Secure Select (niPGT-A)

Chromosome screening from the embryo’s culture fluid — used alongside, not instead of, biopsy PGT-A.

Carrier and Reproductive Risk

4 tests

Understanding what parents may pass on.

Secure Match

Checks both partners for recessive conditions they could pass on.

Secure Risk

By consultation

Polygenic risk scoring for adults, for common complex conditions.

KIR-HLA-C

Types maternal KIR and partner HLA-C, an emerging marker studied in implantation failure.

Thrombophilias

Factor V Leiden and prothrombin variants, tested in selected cases.

Female Factor

2 tests

Investigating female-side fertility.

Karyotype (female)

Full chromosome check from a blood sample.

FMR1 / POI

Fragile-X changes linked to early loss of ovarian function.

Male Factor

5 tests

Investigating male-side fertility.

Sperm FISH

Counts chromosome errors directly in sperm.

Y-microdeletions

Missing pieces of the Y chromosome that affect sperm production.

CFTR / CBAVD

Cystic-fibrosis gene changes linked to blocked or absent sperm ducts.

Karyotype (male)

Full chromosome check from a blood sample.

Sperm DNA Fragmentation

DNA damage in sperm, associated with fertilisation and pregnancy-loss outcomes.

Prenatal

5 tests

Testing during an established pregnancy.

Secure Natal (NIPT)

Screens for trisomy 21, 18 and 13 from a maternal blood draw.

Fetal Karyotype

Full chromosome analysis of the baby.

Array-CGH (microarray)

Detects missing or extra chromosome pieces.

QF-PCR

Rapid check for the most common chromosome conditions.

Whole-Exome Sequencing

Deep gene sequencing to find a suspected genetic cause.

Not sure which test?

Your BioBloom clinical team can help you build the right panel for each patient.