echiDNA Pathology Labs Pty Ltd

Site

echiDNA Pathology Labs Pty Ltd

Accreditation No.

20642

Site No.

24747

Date of Accreditation

04 Dec 2025

Address

Level 6, CBCRC Building, 300 Herston Road
Herston, QLD 4006
Australia

bgi.com

Contact

Availability

Services available to external clients

Supervision

Not Applicable

echiDNA Pathology Labs Pty Ltd address map

Scope of Accreditation

Print scopes
echiDNA Pathology Labs Pty Ltd

ISO 15189 (2012)

Human Pathology

  • This facility complies with the relevant National Pathology Accreditation Advisory Council (NPAAC) requirements.
Service Product Determinant

Suspended

Molecular genetics - Assay for defined mutation or polymorphism (including pharmacogenetic testing) - Whole genome sequencing studies for inherited (germline) DNA/RNA changes		 Extracted DNA Variants in the nuclear genome

ISO 15189 (2022)

Human Pathology

  • This facility complies with the relevant National Pathology Accreditation Advisory Council (NPAAC) requirements.
Service Product Determinant
Molecular genetics - DNA extraction Blood Viable DNA; Viable DNA for sequencing
Plasma Viable DNA
Molecular genetics - DNA fragment size analysis Extracted DNA DNA fragment size determination
Molecular genetics - DNA sequencing Extracted DNA Sequenced DNA
Inherited (germline) whole exome sequencing; Sequenced DNA utilising massively parallel sequencing technologies
Molecular genetics - Investigation of constitutional genetic variants - Carrier testing - Targeted genes Blood; Extracted DNA Fragile X
Molecular genetics - Investigation of constitutional genetic variants - Carrier testing - Targeted panels for inherited (germline) DNA/RNA changes Blood; Extracted DNA Autosomal recessive single gene disorders; X-linked single gene disorders
Molecular genetics - Non-invasive prenatal (genetic) screening Extracted DNA; Maternal plasma Aneuploidy for chromosomes X and Y; Jacobs syndrome (XYY); Klinefelter syndrome (XXY); Rare autosome aneuploidy and segmental genomic imbalances; Trisomy 13, trisomy 18, trisomy 21; Trisomy X; Turners syndrome (SCA:XO)
Molecular genetics/Cytogenetics - Bioinformatic analysis DNA sequences Primary analysis - Conversion of instrument file to FASTQ or FASTA file; Secondary analysis - Alignment and variant calling; Tertiary analysis - Data annotation and interpretation

The only data displayed is that deemed relevant and necessary for the clear description of the activities and services covered by the scope of accreditation.

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