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May 14, 2012 at 8:00 AM - 9:00 AM
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Transcriptome sequencing, RNA-Seq, is a powerful tool to determine expression levels of various transcripts using shallow sequencing approaches. However to find novel splice variants, gene fusions and rare transcripts deeper sequencing is required.
This webinar will cover:
• How The Agilent's SureSelect RNA Capture solutions allow you to achieve depth to focusing your research on the regions that matter most to you, while maintaining relative gene expression levels.
• How research on smaller subsets you can find novel splice variants and gene fusions that are frequently associated with disease.
JOIN US FOR THIS UPCOMING WEBINAR
Register Now
Transcriptome sequencing, RNA-Seq, is a powerful tool to determine expression levels of various transcripts using shallow sequencing approaches. However to find novel splice variants, gene fusions and rare transcripts deeper sequencing is required.
This webinar will cover:
• How The Agilent's SureSelect RNA Capture solutions allow you to achieve depth to focusing your research on the regions that matter most to you, while maintaining relative gene expression levels.
• How research on smaller subsets you can find novel splice variants and gene fusions that are frequently associated with disease.
JOIN US FOR THIS UPCOMING WEBINAR
