Gene expression of the transcriptome using common oncology biospecimens such as degraded FFPE is a substantial challenge to RNA-Seq adoption, which results in the loss of small and rare transcripts in transcriptome analysis.
A novel and streamlined workflow which combines library preparation and post-library ribosomal RNA (rRNA) depletion enables the ability to construct a more complex library from FFPE RNA that includes both long and short RNA biotypes and is therefore more representative of the complete transcriptome.
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