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RNA-Seq allows you to discover and profile the entire transcriptome in any organism.

With no probes or primers to design, RNA-Seq delivers unbiased and unparalleled information about the transcriptome.

RNA-Seq supports both genome-wide expression discovery and profiling, enabling the discovery and measurement of transcript abundance over five orders of magnitude, and accurately quantify tissue-specific isoforms.

This enables the generation of full sequence date from any poly-A tailed RNA to analyze novel transcripts, novel isoforms, alternative splice sites, rare transcripts, and cSNPs in one experiment.

Sequencing-based RNA analysis records the numerical frequency of a sequence in the library population, eliminating background signals observed using relative expression profiles generated with microarray hybridizations.

RNA-Seq offers a new level of assay customizability to optimize each experiment to a study’s specific design and purposes.

The sequencing data is essentially digital (numerical frequency of discrete mapped reads) so coverage depth can be tuned by simply sequencing more or less of the sample.

This customizable depth enables a range of applications, from expression profiling and sample classification with low read count to rare transcript or variant discovery with deep coverage.

RNA-Seq Sample Submission

*Recommended sample submission type

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