Illumina TruPath Genome

Illumina TruPath™ Genome transforms human whole-genome sequencing by combining the accuracy of short-read sequencing with long-range genomic insights. Powered by proximity mapped read technology and designed for use with the NovaSeq™ X Series and DRAGEN™ Germline analysis, TruPath Genome simplifies WGS with approximately 10 minutes of hands-on preparation time while enabling comprehensive variant detection, improved structural variant resolution, and ultralong phasing. Key features include:

• Simplified workflow: Approximately 10 minutes of hands-on preparation time, eliminating traditional library preparation steps
• Long-range genomic insights: Uses proximity mapped read technology to preserve long-distance DNA information
• Improved coverage: Helps resolve difficult-to-map, repetitive, homologous, and duplicated genomic regions
• High-accuracy variant calling: Supports detection of SNVs, indels, CNVs, structural variants, and phased variant calls
• Enhanced structural variant detection: Improves SV resolution and enables visualization of complex rearrangements
• Ultralong phasing: Produces phase blocks extending from hundreds of kilobases to several megabases
• NovaSeq X Series integration: Runs on NovaSeq X and NovaSeq X Plus Systems with C2 or C8 flow cell configurations

For Research Use Only.

Not for use in diagnostic procedures (except as specifically noted).