The IP-Star® Compact System: An Automated Method for Efficient, Accurate and Reproducible Construction of RNA-seq Libraries

19 Oct 2014

The pairing of traditional expression assays with high-throughput sequencing (RNA-seq) has allowed the generation of genome-wide gene expression data with unparalleled specificity, throughput, and sensitivity delivering an unbiased representation of the transcriptome. However, full genome transcriptional gene characterization has been partially limited by the complexity and increased time-requirements of available RNA-seq library construction protocols. Here we report the successful application of the Diagenode IP-Star® Compact System for the easy, rapid, and reproducible RNA-seq library construction of five Mus musculus (mouse) samples. Use of the IP-Star® Compact System significantly reduces the hands-on time required and results in high-quality, highly reproducible RNA-seq libraries tailored for Illumina high-throughput next-generation sequencing. The IP-Star® Compact System is an efficient and reliable tool for the construction of next-generation RNA-seq libraries, especially for transcriptome-based annotation of larger genomes or genomes with many alternative gene isoforms.

SX-8G IP-Star® Compact Automated System

Diagenode

Chromatin immunoprecipitation and DNA methylation assays followed by next generation sequencing is a powerful technique for generating genome-wide profiles of epigenetic modifications and transcription factor binding sites. The SX-8G IP-Star® Compact Automated System provides the flexibility needed to change multiple parameters in the protocols to achieve optimal experimental conditions. Samples generated on the system are compatible with popular downstream applications such as QPCR, microarrays and next generation sequencing platforms. In addition to automated ChIP and DNA methylation protocols, this system contains a wide variety of protocols including next generation sequencing library preparation and sample purification. Easy-to-use user interface for protocol optimization Magnetic-bead technology for great reproducibility Reduced "hand on time" to just only 15 minutes Easy to use bench-top liquid handling system Process up to 16 samples in parallel True "walk-away" automation Flexibility to adapt your experimental condition

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Genome AnalysisGenomics, the study of genomes, includes functional genomics, evolutionary genomics and comparative genomics. There are many genomic technologies such as DNA sequencing of whole genomes, computational biology and bioinformatics. DNA and nucleic acids must be isolated and concentrated from cells for analysis with kits, automated analyzers and software. Other useful technologies for studying genomics include PCR, microarrays and electrophoresis.Next Generation SequencingNext-generation sequencing (NGS), also known as whole-genome sequencing, high-throughput sequencing and massive parallel sequencing, produces and analyses thousands to millions of nucleotide sequences at once. Sequencing systems operate via varying technologies depending on the manufacturer, including sequencing by synthesis, ligation, pyrosequencing, ion semiconductor and single-molecule real-time sequencing. For NGS, library preparation is paramount to successful sequencing. In this section, explore a range of library preparation kits, from targeted, amplicon-based or hybridization-based kits including epigenomic, transcriptomic and genomic workflows to fragmentation kits. Find the best next-generation sequencing products in our peer-reviewed product directory: compare products, check customer reviews and receive pricing direct from manufacturers.Library GenerationLibrary generation refers to the construction of NGS libraries from RNA and DNA sources.RNA-SeqRNA sequencing (RNA-seq) is a next-generation sequencing technique used to analyze the transcriptome, providing insights into gene expression and regulation. This method is essential for genomics, disease research, and personalized medicine. Explore RNA-seq tools in our peer-reviewed product directory; compare products, check reviews, and get pricing directly from manufacturers.High ThroughputHigh throughput experiments allow the simultaneous processing of several samples. This parallelization reduces the cost per experiment and increases reproducibility and output volume of data.
The IP-Star® Compact System: An Automated Method for Efficient, Accurate and Reproducible Construction of RNA-seq Libraries