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README.md: Added ref to downstream analyses #1060

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Aug 16, 2023
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README.md: Added ref to downstream analyses #1060

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README.md: Pointer to downstream workflow 'differential abundance'
smoe Jul 13, 2023
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Update README.md
drpatelh Aug 2, 2023
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Expand Up @@ -95,6 +95,8 @@ To see the results of an example test run with a full size dataset refer to the
For more details about the output files and reports, please refer to the
[output documentation](https://nf-co.re/rnaseq/output).

This pipeline assigns the RNA/cDNA reads to genes in the genome, counts the number of reads per gene and normalizes the data. It does not compare the samples or assign P values to individual genes. For downstream analyses, the output files can be analysed directly in statistics environments like [R](https://www.r-project.org/) or [Julia](https://julialang.org/), or be forwarded to another workflow of Nextflow to determine transcripts with [differential abundance](https://github.com/nf-core/differentialabundance/).
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## Online videos

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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