8 lines
416 B
Markdown
8 lines
416 B
Markdown
This workflow can be used for the following:
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+ Identify RNA transcripts using either cDNA or direct RNA reads.
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+ Reference aided transcriptome assembly.
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+ Annotation of assembled transcripts.
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+ Gene fusions detection.
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+ Differential gene expression analysis using a pre-computed or assembled reference transcriptome.
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+ Differential transcript usage analysis using a precomputed or assembled reference transcriptome. |