Workflows
What is a Workflow?Filters
dada2 amplicon analysis for paired end data
The workflow has three main outputs:
- the sequence table (output of makeSequenceTable)
- the taxonomy (output of assignTaxonomy)
- the counts which allow to track the number of sequences in the samples through the steps (output of sequence counts)
This workflow performs segmentation and counting of cell nuclei using fluorescence microscopy images. The segmentation step is performed using Otsu thresholding (Otsu, 1979). The workflow is based on the tutorial: https://training.galaxyproject.org/training-material/topics/imaging/tutorials/imaging-introduction/tutorial.html
Assemble long reads with Flye, then view assembly statistics and assembly graph
Run velocyto to get loom with counts of spliced and unspliced. It will extract the 'barcodes' from the bundled outputs.
MMGBSA simulation and calculation
Run baredSC in 1 dimension in logNorm for 1 to N gaussians and combine models.
Automated inference of stable isotope incorporation rates in proteins for functional metaproteomics
We assume the identifiers of the input list are like: sample_name_replicateID. The identifiers of the output list will be: sample_name
Racon polish with long reads, x4
Downloads fastq files for sequencing run accessions provided in a text file using fasterq-dump. Creates one job per listed run accession.
Tests