InView Transcriptome Products
Choose the perfect package for your application
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INVIEW
Transcriptome Explore
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INVIEW
Transcriptome Discover
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INVIEW
Transcriptome
Isoform Discover
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Reliable transcript identification and comparison between expression levels
Improve sensitivity and reduce bias in transcriptome profiling using NGS-based RNA sequencing with expert library preparation and in-depth analysis.
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Discover and quantify novel transcripts and splicing variants
NGS-based RNA-seq of strand-specific libraries for profiling of rare, novel transcripts or for analysing splicing variants even without a reference sequence
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Isoform sequencing with PacBio's long-read technology to precisely identify new spicing variants
Use PacBio's ultra-long reads to cover full-length cDNA and perform genome-wide analysis of transcript isoform variations.
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Comparison
Product
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Explore |
Discover |
| Library type |
Strand-specific cDNA |
| Starting material |
Application for total RNA from various sources, starting from one sample
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| Sequencing technology |
Illumina
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| Read mode |
50 bp single reads
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150 bp paired-end reads |
| Number of guaranteed reads |
Multiples of 30M single reads
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Multiples of 30M read pairs |
| Delivery |
Express delivery time starts at 17 working days
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Very well suited for:
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Novel transcripts
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- |
+ |
Strand specifity information
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- |
+ |
Rare transcripts
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Flexible increase of data output |
Splice variants
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- |
+ |
Transcript identification
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+ |
++(+) |
Differential expression
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+ |
++(+) |
Mapping accuracy
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High |
Flexible |
High quality reference
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Mandatory |
Additional |
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Available additional services:
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RNA isolation *
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+ |
+ |
RNA depletion *
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+ |
+ |
Bioinformatic analysis
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+ |
+ |
* dependent on sample source