A cloud LIMS that tracks samples, tests results, and manages inventory for life science research, industrial QC labs, and biotech/NGS. Includes regulatory support for CLIA and HIPAA, Part 11 and ISO 17025. The quality, security, traceability, and traceability for samples is crucial to a lab's success. Laboratory professionals can use the Lockbox LIMS system to manage their samples. They have full visibility of every step of the sample's journey from accession to long-term storage. LIMS analysis is more than just tracking results. Lockbox's multilayered sample storage and location management functionality lets you define your lab's storage structure using a variety location options: rooms and storage units, shelves and racks, boxes and boxes.
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Labs don't need another LIMS. They need a complete operating system for modern lab operations - and that's QBench, reshaping everything from order placement through sample processing to automated reporting.
Simple. Powerful. Adaptable. Where other LIMS force labs into rigid structures built on heavy custom code and vendor dependency, QBench moves with you. It bends. It adapts. Your processes evolve, and QBench evolves too.
It adapts to your secret sauce. Every lab has its own workflow, its own rhythm, and QBench respects that with unmatched configurability. You shape the workflows. You define the data fields. You stitch together the automations. QBench's former bench scientists work alongside you throughout, offering expert guidance and workflow suggestions.
It automates the tedious work. File parsers and a robust API connect QBench to the instruments and systems you already run, so data flows on its own. No manual entry. No transcription errors.
It unifies everything in one platform. Real-time inventory. A dedicated portal giving clients instant access to results. Built-in analytics. A QMS module that keeps you audit-ready, always.
QBench helps labs work smarter - cloud-based, secure, and always evolving, like the science it supports.
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QIAGEN CLC Genomics Workbench
The QIAGEN CLC Geneomics Workbench is a powerful tool that works for all workflows. It is easy to overcome data analysis challenges with cutting-edge technology, unique features and algorithms that are widely used by scientists in industry and academia. Bioinformatics software solutions that are user-friendly allow for comprehensive analysis and interpretation of your NGS data. This includes de novo assembly and transcriptome assembly, resequencing analysis, WES and targeted panel support, variant calling, variant calling, RNA–seq, ChIP–seq and DNA methylation analysis (bisulfite sequence analysis). You can analyze your RNA-seq (miRNA, smallRNA) and smallRNA (lncRNA), data using easy-to-use transcriptomics workflows that allow for differential expression analysis at both gene and transcript levels. QIAGEN CLC Genomics Workbench was designed to support a wide variety of NGS bioinformatics programs.
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Genome Analysis Toolkit (GATK)
Created within the Data Sciences Platform at the Broad Institute, this comprehensive toolkit provides an extensive array of features primarily aimed at variant discovery and genotyping. With its robust processing engine and high-performance computing capabilities, it is equipped to manage projects of any magnitude. The GATK has established itself as the industry benchmark for detecting SNPs and indels in both germline DNA and RNA sequencing data. Its functionalities are now broadening to encompass somatic short variant detection as well as addressing copy number variations (CNV) and structural variations (SV). Besides the core variant callers, the GATK incorporates numerous utilities for executing associated tasks, including the processing and quality assurance of high-throughput sequencing data, and it comes bundled with the well-known Picard toolkit. Originally designed for exome and whole genome data generated via Illumina sequencing technology, these tools are versatile enough to be modified for use with various other technologies and study designs. As research evolves, the adaptability of the GATK ensures it remains relevant in diverse genomic investigations.
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