:
toolshed.g2.bx.psu.edu/repos/iuc/multiqc/multiqc/1.27+galaxy4
Metadata
Links
Observed Tool Versions
Within GTN tutorials
1.27+galaxy4
1.27+galaxy3
1.24.1+galaxy0
1.11+galaxy1
1.11+galaxy0
1.9
1.9+galaxy1
1.8+galaxy1
1.8+galaxy0
1.7
1.2.0
Relevant Tutorials
- Assembly / Unicycler assembly of SARS-CoV-2 genome with preprocessing to remove human genome reads
- Assembly / An Introduction to Genome Assembly
- Assembly / Hybrid genome assembly - Nanopore and Illumina
- Assembly / Large genome assembly and polishing
- Assembly / Unicycler Assembly
- Contributing to the Galaxy Training Material / Creating content in Markdown
- Ecology / Data submission using ENA upload Tool
- Ecology / RAD-Seq Reference-based data analysis
- Epigenetics / CUT&RUN data analysis
- Using Galaxy and Managing your Data / Annotate, prepare tests and publish Galaxy workflows in workflow registries
- Genome Annotation / CRISPR screen analysis
- Introduction to Galaxy Analyses / NGS data logistics
- Introduction to Galaxy Analyses / Very Short Introductions: QC
- Microbiome / Metatranscriptomics analysis using microbiome RNA-seq data
- Microbiome / Metatranscriptomics analysis using microbiome RNA-seq data (short)
- Microbiome / MGnify v5.0 Amplicon Pipeline
- Microbiome / 16S Microbial analysis with Nanopore data
- Microbiome / Pathogen detection from (direct Nanopore) sequencing data using Galaxy - Foodborne Edition
- Sequence analysis / Mapping
- Sequence analysis / Quality Control
- Single Cell / Pre-processing of Single-Cell RNA Data
- Single Cell / Pre-processing of 10X Single-Cell RNA Datasets
- Transcriptomics / Genome-wide alternative splicing analysis
- Transcriptomics / De novo transcriptome assembly, annotation, and differential expression analysis
- Transcriptomics / Pathway analysis with the MINERVA Platform
- Transcriptomics / Whole transcriptome analysis of Arabidopsis thaliana
- Transcriptomics / Reference-based RNA-Seq data analysis
- Transcriptomics / 1: RNA-Seq reads to counts
- Variant Analysis / Exome sequencing data analysis for diagnosing a genetic disease
- Variant Analysis / From NCBI's Sequence Read Archive (SRA) to Galaxy: SARS-CoV-2 variant analysis
- Variant Analysis / Somatic Variant Discovery from WES Data Using Control-FREEC
- Variant Analysis / Identification of somatic and germline variants from tumor and normal sample pairs
- Variant Analysis / M. tuberculosis Variant Analysis