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Merge pull request #1060 from smoe/patch-1
README.md: Added ref to downstream analyses
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README.md

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@@ -95,6 +95,8 @@ To see the results of an example test run with a full size dataset refer to the
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For more details about the output files and reports, please refer to the
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[output documentation](https://nf-co.re/rnaseq/output).
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This pipeline quantifies RNA-sequenced reads relative to genes/transcripts in the genome and normalizes the resulting data. It does not compare the samples statistically in order to assign significance in the form of FDR or P-values. For downstream analyses, the output files from this pipeline can be analysed directly in statistical environments like [R](https://www.r-project.org/), [Julia](https://julialang.org/) or via the [nf-core/differentialabundance](https://github.com/nf-core/differentialabundance/) pipeline.
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## Online videos
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A short talk about the history, current status and functionality on offer in this pipeline was given by Harshil Patel ([@drpatelh](https://github.com/drpatelh)) on [8th February 2022](https://nf-co.re/events/2022/bytesize-32-nf-core-rnaseq) as part of the nf-core/bytesize series.

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