NextGENe®LR Analysis Software for Long-Read Sequencing

Transform complex genetic data into actionable insights

Efficiently analyze data from Pacific Biosciences systems, plus Oxford Nanopore instruments with up to 98% accuracy.

Why Researchers Choose NextGENeLR

Precision Analysis

• Detect SNVs & indels at frequencies as low as 2%
• Identify complex structural variants with homopolymer compression
• Resolve mitochondrial mixtures with 0.1% sensitivity
• Assist with Haplotype determination

Scientist-Friendly Design

• Intuitive interface designed for domain experts, not coders
• Process multiple samples in batches
• One-click workflows from raw data to reports

Visual Insights

• Interactive alignment viewers with integrated variant tables
• Color-coded STR displays (normal/premutation/pathogenic)
• Deliver publication-ready visuals and standard formats (BAM/VCF)

Key NextGENeLR Applications

Structural Variation Detection

Reliably identify insertions, deletions, and translocations through specialized long-read alignment with homopolymer compression technology. Traditional short-read technologies often miss critical structural variations that NextGENeLR can accurately detect and visualize.
Learn more about Structural Variation Detection

Whole Genome Mitochondrial DNA Analysis

Analyze complete mitochondrial sequences in as few as two amplicons, with variant detection down to 0.1% for minor haplotypes. Our Haplotype Reports deliver precise mitochondrial haplotyping results even for challenging samples.
Learn more about Mitochondrial DNA Analysis

STR Expansion Analysis

Precisely measure disease-associated repeat lengths with color-coded visualization of normal, premutation, and pathogenic ranges for neurological disorders.
Learn more about STR Expansion Analysis

Get Started with NextGENeLR

From raw data to actionable discoveries, NextGENeLR empowers domain experts to unlock the full potential of long-read sequencing technologies. Transform your long-read sequencing analysis with NextGENeLR's powerful combination of precision, ease of use, and visual insights.

Whether you're analyzing SNVs/small Indels, structural variations, mitochondrial DNA, or STR expansions, our specialized algorithms and intuitive interface eliminate bioinformatics bottlenecks and deliver publication-ready results.