Workflows
What is a Workflow?Filters
RNASeq-DE @ NCI-Gadi processes RNA sequencing data (single, paired and/or multiplexed) for differential expression (raw FASTQ to counts). This pipeline consists of multiple stages and is designed for the National Computational Infrastructure's (NCI) Gadi supercompter, leveraging multiple nodes to run each stage in parallel.
Infrastructure_deployment_metadata: Gadi (NCI)
A prototype implementation of the Air Quality Prediction pipeline in Galaxy, using CWL tools.
Lysozyme in Water simplest version, from COMPSs Tutorial. The original idea of this worklfow comes from http://www.mdtutorials.com/gmx/lysozyme/index.html
ABR_Threshold_Detection
What is this?
This code can be used to automatically determine hearing thresholds from ABR hearing curves.
One of the following methods can be used for this purpose:
- neural network (NN) training,
- calibration of a self-supervised sound level regression (SLR) method
on given data sets with manually determined hearing thresholds.
Installation:
Run inside the src directory:
Installation as python package
pip install -e ./src (Installation as python
...
An example workflow for the Specimen Data Refinery tool, allowing an individual tool to be used
Type: Galaxy
Creators: Laurence Livermore, Oliver Woolland, Oliver Woolland
Submitter: Oliver Woolland
An example workflow for the Specimen Data Refinery tool, allowing an individual tool to be used
An example workflow to allow users to run the Specimen Data Refinery tools on data provided in an input CSV file.
StructuralVariants Workflow
Type: Common Workflow Language
Creators: Laura Rodriguez-Navas, Daniel López-López
Submitter: Laura Rodriguez-Navas
VGP Workflow #1
This workflow produces a Meryl database and Genomescope outputs that will be used to determine parameters for following workflows, and assess the quality of genome assemblies. Specifically, it provides information about the genomic complexity, such as the genome size and levels of heterozygosity and repeat content, as well about the data quality.
Inputs
- Collection of Hifi long reads in FASTQ format
Outputs
- Meryl Database of kmer counts
- GenomeScope
- Linear plot
...
VGP Workflow #1
This workflow collects the metrics on the properties of the genome under consideration by analyzing the k-mer frequencies. It provides information about the genomic complexity, such as the genome size and levels of heterozygosity and repeat content, as well about the data quality. It uses reads from two parental genomes to partition long reads from the offspring into haplotype-specific k-mer databases.
Inputs
- Collection of Hifi long reads in FASTQ format
- Paternal short-read ...