VariFind™ PULM Assay
NGS-based assay for for detection of clinically significant genetic variants in 83 genes associated with pulmonary diseases and related conditions

Intended use: molecular-genetic investigation of pulmonary diseases and related conditions
Disordes included
Acute respiratory distress
Spontaneous family pneumothorax
Pulmonary hypertension
Lymphangioleiomyomatosis
BPCO
Primary ciliary dyskinesia
Pulmonary fibrosis
Emphysema
Hereditary pulmonary alveolar proteinosis
Acute nocturnal respiratory distress
Pulmonary cysts
Cystic fibrosis
Bronchiectasis
Genes included
Assay information
Analyzed region
CDSs + 20 bp padding (except CFTR)
For CFTR: CDSs + UTRs
Target region size
469 kb
Platform
Illumina MiSeq Series
Product composition
Reagents kit
Targeted enrichment , library preparation, molecular barcoding
VariFind™ Software for
MPS data analysis & variants annotation
Assay workflow
NGS Libraries Preparation
Sequencing
Automated data analyis & annotation
Report generation
Made on
Tilda