Explore the advanced sequencing, molecular biology, automation, and data management platforms that power BaseClear’s high-quality analytical and genomics services.
BaseClear’s Technology Platforms provide clients with access to a comprehensive portfolio of advanced sequencing, molecular biology, automation, and laboratory information management technologies. Whether supporting microbial genomics, biopharmaceutical development, quality control, strain characterization, contamination testing, or large-scale research projects, these platforms enable the generation of accurate, reliable, and actionable data. Clients benefit from access to the most appropriate technology for their specific application, ranging from high-throughput sequencing and long-read analysis to highly sensitive nucleic acid quantification and automated laboratory workflows.
What makes BaseClear distinctive is the integration of these technologies within a single organization, supported by experienced scientists, bioinformaticians, and project managers. Rather than offering individual instruments or standalone services, we combine leading platforms such as Ultima, Illumina, Oxford Nanopore, Sanger sequencing, dPCR, qPCR, Tecan automation, and LabWare LIMS to create efficient, scalable, and fit-for-purpose workflows. This integrated approach delivers high-quality data, improved turnaround times, full traceability, and a seamless customer experience from sample receipt to final results.
BaseClear offers a broad portfolio of sequencing, PCR, automation, and laboratory information management platforms, including Ultima, Illumina, Oxford Nanopore, Sanger, dPCR, qPCR, Tecan, and LabWare. This allows our scientists to select the most appropriate technology for each project rather than forcing every application onto a single platform.
Our technology platforms are connected through automated laboratory workflows, in-house bioinformatics, and LabWare LIMS and ELN systems. Clients benefit from complete sample traceability, reduced manual handling, improved reproducibility, and a seamless process from sample receipt to final reporting.
The same technology infrastructure supports projects ranging from routine research studies to GMP-compliant biopharmaceutical testing and validation programs. Combined with our GMP license, ISO 17025 accreditation, and ISO 27001 certification, clients can confidently scale projects while maintaining quality, compliance, and data integrity.
The best sequencing solution depends on the biological question, timeline, and data requirements of the project. TurboSeq is designed for rapid turnaround, UltraScale Sequencing for large-scale and cost-efficient data generation, Hybrid Sequencing for maximum genomic resolution through combined short- and long-read sequencing, and RNA-Seq for gene expression profiling and transcriptomic analysis. BaseClear works with clients to select the most appropriate workflow based on project goals, sample type, budget, and desired outcomes.
Hybrid Sequencing provides advantages when both high accuracy and long-range genomic information are required. By combining Illumina short reads with Oxford Nanopore long reads, the approach improves genome assembly quality, resolves repetitive genomic regions, enhances taxonomic classification, and supports more detailed interpretation of complex microbial communities and genomes than either technology alone.
Turnaround times vary depending on the sequencing solution selected and the complexity of the project. Genome in a Week can deliver assembled microbial genomes within five business days, while TurboSeq provides high-quality sequencing data in as little as one week from sample receipt. Larger projects involving RNA-Seq, Hybrid Sequencing, or UltraScale Sequencing may require additional analysis time depending on study size and deliverables.
Every Advanced Sequencing Solution includes quality control measures throughout sample processing, library preparation, sequencing, and bioinformatics analysis. Depending on the service, clients receive detailed QC metrics such as DNA or RNA quality assessments, library quality statistics, sequencing yield, read quality metrics, control performance, and bioinformatics QC summaries to ensure that generated data meet predefined acceptance criteria.
Advanced Sequencing Solutions provide both raw sequencing data and project-specific analytical outputs tailored to the scientific objectives. Depending on the selected service, deliverables may include FASTQ files, genome assemblies, transcriptomic datasets, gene expression tables, variant analyses, taxonomic profiles, publication-ready visualizations, comprehensive reports, and expert interpretation to support research, development, quality control, and regulatory activities.
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