scWGS, structural variant detection, and bespoke DNA analysis.
We offer a fully automated single-cell Whole Genome Sequencing (scWGS) pipeline developed in-house, leveraging our proprietary integration of the Aneufinder algorithm for Copy Number Variation (CNV) detection. Our platform resolves structural variants and aneuploidy down to 40kb in individual cells, providing unparalleled insights into cancer evolution and genomic instability. Complementing this, we offer Shallow Mini-Bulk WGS for cost-effective profiling and Long-Read DNA Sequencing (Oxford Nanopore) for complex structural analysis and methylation profiling.
End-to-end automation from single-cell sorting to library prep, minimizing bias and maximizing throughput for tumor heterogeneity studies.
Our in-house pipeline utilizes advanced algorithms (based on Aneufinder) to detect CNVs, aneuploidy, and subclonal populations with high precision, even in low-coverage data.
Oxford Nanopore reads (>100kb) to resolve complex rearrangements, translocations, and simultaneous DNA methylation profiling.
Custom pipelines for Whole Exome Sequencing (WES), circulating tumor DNA (ctDNA/cfDNA) analysis, and targeted structural variant detection.
Tracking tumor progression, resistance mechanisms, and metastatic spread at single-cell resolution.
Detecting minimal residual disease and early-stage cancer signals from blood samples.
High-depth Exome Sequencing for identifying somatic mutations in driver genes and rare variants.
Characterizing large-scale chromosomal aberrations in 3D culture models to ensure model fidelity.
Integrating ATAC-seq data to map chromatin accessibility and regulatory landscapes in disease contexts.
Our automated scWGS pipeline — from single-cell isolation to copy number calling.
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Our automated pipeline detects copy number variations down to 40kb resolution in individual cells, using our proprietary Aneufinder-based analysis.
Yes. We offer WES alongside scWGS and can combine both approaches for comprehensive genomic profiling.
Tell us about your project and we'll scope a solution for your lab.
