NextGENeLR delivers enhanced precision, streamlined workflows, and powerful reporting tools to address critical challenges in long-read sequencing analysis.
Designed for PacBio® and Oxford Nanopore® data, NextGENeLR now makes complex variant detection and interpretation accessible to all researchers without compromising accuracy.
NextGENeLR delivers major advancements in variant detection accuracy and interpretive power designed specifically for the demands of long-read sequencing. From single-nucleotide changes to complex genomic rearrangements, these innovations redefine precision in genomic analysis.
Whether you're investigating inherited disorders, infectious diseases, or structural variations, these new tools provide the clarity and reliability needed for confident discovery.
NextGENeLR’s updated algorithms now identify and filter common noise patterns, significantly improving the accuracy of SNV and short indel detection.
Overcome the limitations of short-read technologies with reliable detection of large insertions, deletions and translocations—all from a single analysis pipeline.
Sequence the entire mitochondrial genome in just 2 amplicons, enabling high-resolution analyses for haplotyping and disease research.
NextGENeLR puts powerful long-read analysis directly in the hands of biologists and clinicians through its intuitive graphical interface.
Designed specifically for domain experts, it eliminates coding barriers with guided, one-click workflows—seamlessly integrating every step from raw data processing to final report generation in a single, user-friendly environment.
NextGENeLR requires no bioinformatics expertise—its intuitive interface combines analysis, visualization, and reporting in one unified workspace, eliminating complex scripting. Researchers can effortlessly run a batch of new samples while simultaneously reviewing the results of a previous project in the viewer.
NextGENeLR is capable of delivering publication-ready results with high-resolution visualizations of BAM alignments, haplotyping results and STR expansion profiles. The platform also provides a variety of output options, generating both standardized analysis files (BAM, annotated VCF) and textual outputs for seamless sharing and collaboration.
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