Cost-Effective Workflow for Sequencing Applications from Illumina

5 Nov 2010
Sarah Sarah
Marketing / Sales

Product news

Illumina introduces TruSeq™ Sample Prep and Exome Enrichment Kits. TruSeq sequencing reagents provide a streamlined workflow that is economical and scalable, delivering industry-leading accuracy for sequencing studies.

“The benefits of TruSeq are critical for our customers who are routinely generating more than 300 Gb per run with their HiSeq systems,” said Christian Henry, General Manager of Life Sciences for Illumina. “As we continue to scale the output of our HiSeq systems, the multiplexing capability and economics of TruSeq solutions will become even more important. Illumina is committed to continuing innovation in sequencing to help our customers do more and publish even faster. In fact, the 1,000th study using Illumina sequencing was published in October.”

TruSeq Sample Prep kits feature master-mixed reagents and optimized adapter design, making the industry’s most simplified sequencing workflow even easier. TruSeq Exome Enrichment kits, used with TruSeq DNA Sample Prep kits, enable large-scale exome studies using a pre-enrichment pooling approach with plate-based processing of up to 96 samples.

“The RNA Sample Prep Kit allows us to take full advantage of the increased sequencing output of our Illumina instruments,” said Greg May, President and COO at the National Center for Genomic Resources. “RNA-seq is now cost-competitive with microarrays, allowing the design of reasonably priced, rigorous gene expression experiments with appropriate sample sizes for statistical analysis.”

TruSeq solutions provide:
• Coverage of greater than 62 Mb of the human exome, with an industry-leading price of less than $300 per sample enrichment.
• A flexible approach for single-end, paired-end, and multiplexed sequencing with as much as 80% reduction in price for sample prep.
• Sequencing-based gene expression studies with richer data sets, a simpler workflow, and a lower price than arrays.
• A means for researchers to combine up to 48 samples into a single sequencing lane, profiling the whole spectrum of small RNAs with the highest sensitivity and specificity.

TruSeq Sample Prep kits are available for order and expected to ship later this month. For more information about TruSeq kits or to learn more about Illumina’s sequencing workflow solutions please follow the Company article page link top right of this page.

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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.DNA SequencingDNA sequencing, such as sanger sequencing, is a biological technique that determines the precise order of nucleotide bases in a fragment or template of DNA. DNA sequencers and genetic analyzers are based on capillary electrophoresis, where labeled DNA fragments are electrophoretically separated by size as they migrate through a polymer. Find the best DNA sequencing products, including DNA sequencing kits, genomic libraries and genetic identity kits in our peer-reviewed product directory: compare products, check customer reviews and receive pricing direct from manufacturers.RNA InterferenceRNA interference (RNAi) uses siRNA or miRNA for transcriptional silencing, gene knockdown and regulation of gene expression. RNAi requires chemical synthesis, introduction of DNA vectors into cells, an assay of RNAi effects and RNAi quantification or analysis. Consider target sequence selection, reagent preparation, controls, high specificity and effectiveness and low non-specific gene knockdown.
Cost-Effective Workflow for Sequencing Applications from Illumina