Newborn screening

NGS-based assay for testing of cystic fibrosis, phenylketonuria and galactosemia

NGS-based assay for testing of clinically significant variants in CFTR gene associated with cystic fibrosis

NNGS assay for 2nd tier newborn screening of inherited metabolic disorders

NNGS assay for 2nd tier newborn screening of inherited metabolic disorders

Inherited disorders

NGS-based assay for variants detection in 24 genes associated with different types of sugar intolerance

NGS-based assay for detecting of clinically significant genetic variants associated with 19 severe genetic disorders

NGS-based assay for detecting of clinically significant genetic variants associated with 19 severe genetic disorders

Reproductive genetics

NGS-based assay for detecting of clinically significant genetic variants associated with 19 severe genetic disorders

Registry typing

NGS Assay for high-througoutput high-resolution human HLA typing

Custom Assay Service

Service for custom NGS assay design by Parseq Lab.

Data analysis and storage

Infrustructure for genomic data analysis and storage

Application for genome data processing.

Other products

Reference genomic DNA samples with verified mutations in CFTR, PAH и GALT genes.

Biological identificators for sample contamination control.

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