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Parseq Lab

Design and development of diagnostics test systems, targeted assays, software
for sequencing data processing and analysis, infrastructure for genome data storage and analysis, solutions for human identification.
Our products
VariFind™ HID assay. For complex cases in forensics expertise: small amounts of DNA, strongly degraded DNA, DNA mixtures.
Newborn Screening
MPS-based assay for detection of mutations in CFTR, PAH and GALT genes, associated with cystic fibrosis, phenylketonuria and galactosemia.
VARIFIND™ IVF-CS ASSAY for genetic carrier screening in egg and sperm donors and couples planning a family.
Reproductive Genetics
MPS-based assay for genetic carrier screening in egg and sperm donors and couples planning a family.
Parseq Lab provides NGS/MPS data analysis, software design and development.
Human Identification
Solution for human identification based on massively parallel sequencing.
VariFind™ HID assay. For complex cases in forensics expertise: small amounts of DNA, strongly degraded DNA, DNA mixtures.
VariFind™ Software
Application for genome data processing. Designed for primary target sequencing data processing and analysis, quality control
and genetic variants annotation.
Screening for severe inherited diseases: cystic fibrosis and galactosemia by VariFind Neoscreen assay (designed by Parseq Lab).
Custom Assays
Service for targeted high-performance DNA sequencing panels design, developing of tools and databases for genomic data analysis.
Biobank contains reference genomic DNA samples with verified mutations in CFTR, PAH и GALT genes.
Reference Materials
DNA samples with CFTR, PAH and GALT genes.
Parseq Lab team creates customized assays for your research.
Storage and Analysis
Hardware-software appliances for genomic data storage and analysis.
Contacts

Parseq Lab s.r.o.
Czech Republic
info@parseq.pro
http://parseq.pro
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