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Catalog Number | No. of Reactions |
---|---|
4479789 | 48 Reactions |
4475936 | 12 Reactions |
Generally, a successful Ion RNA-Seq library will be within the recommended size range for sequencing on the Ion PGM or Proton systems and the sequencing data will have a high (or expected) percentage of on-target reads.
Find additional tips, troubleshooting help, and resources within our Next-Generation Sequencing Support Center.
Please visit the Transcriptome Sequencing by Ion Torrent Sequencing page (https://www.thermofisher.com/us/en/home/life-science/sequencing/rna-sequencing/transcriptome-sequencing/transcriptome-sequencing-ion-torrent-next-generation-sequencing.html) for information on RNA-Seq data analysis using Torrent Suite Software, or 3rd party software providers.
Find additional tips, troubleshooting help, and resources within our Next-Generation Sequencing Support Center.
The GGCCAAGGCG sequence is part of the RNA library adapter sequence. This sequence can be automatically trimmed by the software by selecting the “RNA_Barcode_None” option under the Barcodes menu. The run can be reanalyzed with the correct barcode settings to trim the adapter sequence. In the future, the “RNA_Barcode_None” option should be selected in the run plan or selected on the instrument prior to starting the sequencing run.
Find additional tips, troubleshooting help, and resources within our Next-Generation Sequencing Support Center.
RNA-Seq relies on a random sampling strategy in which most sequencing reads will identify abundant transcripts with an increasing number of reads needed to identify lower abundant transcripts and/or low levels of gene expression. While depletion and purification strategies are available from Thermo Fisher Scientific to remove unwanted abundant transcripts and increase sequencing power, transcript detection sensitivity is a function of mapped reads. Accordingly, the complexity of the genome under investigation should be taken into account when planning an RNA-Seq experiment. Applications that require a small number of reads, such as low multiplexed gene expression, can be performed on the Ion 318 Chip Using the PGM platform whereas, human/mammalian transcriptomes and highy-multiplexed gene expression profiling should be performed on the GeneStudio platforms, using the higher throughput chips. For more information, please see the Transcriptome Sequencing by Ion Torrent Sequencing page (https://www.thermofisher.com/us/en/home/life-science/sequencing/rna-sequencing/transcriptome-sequencing/transcriptome-sequencing-ion-torrent-next-generation-sequencing.html).
Find additional tips, troubleshooting help, and resources within our Next-Generation Sequencing Support Center.
Another method is chemical fragmentation (not part of the protocol), which is useful for quantifying exon levels, novel splicing identification, and fusion gene discovery, and provides more uniform coverage for viral and bacterial transcripts. Chemical fragmentation is more randomized than RNase III fragmentation, but can be difficult to optimize. Chemically fragmented RNA fragments require repair with T4 polynucleotide kinase (not included in kit) before proceeding into ligation.
Find additional tips, troubleshooting help, and resources within our Next-Generation Sequencing Support Center.
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