Used APPLIED BIOSYSTEMS SoLiD EZ #9090413 for sale

APPLIED BIOSYSTEMS SoLiD EZ is an automated equipment designed to perform high throughput sequencing and library preparation for genomic, transcriptomic, and epigenetic studies. It is a single-use, user-friendly system that is well-suited for laboratories of any size, allowing users to quickly assemble, recharge, and process their samples. This unit includes components such as a controller, reagent carousels, and a barcode scanner which makes sample tracking accurate and efficient. The Genome Analysis Machine featured in SoLiD EZ is a powerful platform for sequencing genomic regions to detect known and unknown variants. This tool enables researchers to capture and sequence entire genomes and amplicon libraries to detect both known and novel mutations. The platform also has the ability to access high-resolution long-read sequencing capabilities to enable higher sensitivity and accuracy in detecting alterations. APPLIED BIOSYSTEMS SoLiD EZ features a comprehensive workflow including automated library preparation, which allows sequence alignments and genotyping of up to 30 samples in one day. Its pipeline also features automated library QC, which leverage real-time monitoring tools to identify and correct potential issues with library quality before use. Furthermore, the asset is designed to analyze samples with low input requirements and determines the presence of rare variants and SNPs with enhanced accuracy. The model also contains adaptive microfluidics technology for large-scale sample analysis and automated sample handling, which is essential for high throughput sequencing. This technology enables bioinformaticians to obtain more accurate and consistent results from single cells or multiple cell compartments simultaneously. Additionally, SoLiD EZ can be used for epigenetic sequencing of DNA methylation patterns, which can be used to understand complex diseases and their treatment. APPLIED BIOSYSTEMS SoLiD EZ is a reliable, efficient, and cost-effective the platform for high-throughput bioinformatics and genomics studies. Its ease of use and workflow automation makes it attractive to laboratories of any size. Its features and versatility enable researchers to perform genotyping, sequencing, and epigenetics in a single easy-to-use platform.