OLC Redmine Automator
The OLC Redmine Automator provides access to genomic data, analysis tools, and data-management workflows through Redmine. Access requires the appropriate organizational network and CFIA Genomics project permissions.
- New users: Getting Started
- General help: Troubleshooting
- Documentation contributions: Adding documentation
Tool and database versions
Automator requests report tool and database versions when available. If a completed request does not report information needed for reproducibility, contact the bioinformatics team and include the Redmine issue number.
Choose a workflow
Import, export, or retrieve data and reports
- External Retrieve — exports raw reads or draft assemblies for local download.
- Report Retrieve — retrieves COWBAT assembly-pipeline reports for requested
SEQIDs. - SRA Download — imports FASTQ data from NCBI SRA and submits it to FoodPort/COWBAT processing.
- SRA Upload — transfers internal raw-read files into an NCBI SRA submission preload folder.
Assess, combine, or reduce raw-read data
- FastQC/MultiQC — creates per-sample read-quality reports and a combined MultiQC report.
- QUAST - evaluates genome assemblies by computing various metrics
- MetaQUAST - evaluates metagenome assemblies by computing various metrics
- Downsample — reduces FASTQ data by coverage, compressed size, read count, base count, sampling fraction, or supported BBMap options.
- Downsample option reference — lists additional supported
reformat.shoptions and defaults. - fastqmerge — combines FASTQ files from multiple sequencing runs of the same biological sample.
Detect genes or run in silico PCR
- GeneSeekr — searches FASTA-formatted assemblies for predefined or attached custom targets.
- Sipprverse — searches raw paired-end FASTQ reads for predefined or custom targets.
- KMA — screens assemblies or raw reads against curated or custom target databases.
- PrimerFinder — performs in silico PCR using VTyper or attached custom primer sets.
Detect or summarize antimicrobial resistance
- ResFinder — detects acquired AMR genes in draft genome assemblies; it does not detect chromosomal point mutations.
- PointFinder — detects supported resistance-associated point mutations in selected genera.
- StarAMR — combines acquired-gene detection with supported mutation detection for Campylobacter and Salmonella assemblies.
- CARD-RGI — predicts resistomes in isolate assemblies or raw FASTQ data.
- AMRsummary — combines acquired-AMR detection with predicted plasmid or chromosome location.
- Plasmid-Borne Identity — searches for user-supplied targets and predicts whether matching targets are plasmid-borne.
GeneSeekr, Sipprverse, and KMA also provide AMR-related target-screening modes. Use their pages when input type or a curated/custom target database determines the workflow choice.
Identify an organism, profile taxonomy, or investigate contamination
- Unknown Isolate — identifies an uncertain isolate assembly using rMLST, Mash, ANIb, and ANIm evidence in a GROBI report.
- StrainMash — identifies the closest represented RefSeq type strain for an assembly.
- AutoCLARK — reports species represented in raw reads or draft assemblies.
- Kraken2/Bracken — performs taxonomic classification and refined abundance estimation using selectable databases.
- MetaPhlAn4 — profiles microbial communities using clade-specific marker genes.
AutoCLARK, Kraken2/Bracken, and MetaPhlAn4 are taxonomic-analysis workflows.
Suspected contamination in raw reads
If you think raw FASTQ reads might be contaminated, run ConFindr. ConFindr checks for evidence of intra-species and inter-species contamination before assembly or downstream analysis.
Do not use Downsample, External Retrieve, or AutoCLARK as substitutes for a ConFindr contamination assessment.
Type an isolate
- MLST — determines an organism- and scheme-specific multilocus sequence type.
- rMLST — performs ribosomal multilocus sequence typing.
- ECTyper — predicts O- and H-antigen serotypes for Escherichia coli assemblies.
- IntiminTyper — assigns intimin (
eae) subtypes to supported E. coli assemblies. - eCGF — performs comparative genomic fingerprinting subtyping for Campylobacter assemblies.
Compare closely related isolates by SNVs or SNPs
- SNVPhyl — analyzes paired-end query reads and produces pairwise SNV counts, core-genome statistics, an alignment, and a Newick tree.
- Snippy — performs rapid variant calling and core alignment, supports paired-end and single-end reads, and can optionally create cleaned IQ-TREE outputs.
- COWSNPhR — calls variants with DeepVariant, maps them to reference annotations, and creates summary tables, alignments, and a FastTree phylogeny.
All three workflows require a suitable reference and closely related query isolates. Their filters and output values are not interchangeable.
Build a tree or select close or diverse genomes
- MashTree — builds a rapid whole-genome distance tree from Mash estimates.
- bcgTree — builds a partitioned maximum-likelihood bacterial tree from essential single-copy core genes.
- NearTree — ranks candidate strains closest to one query within a supplied comparison set.
- CloseRelatives — finds CFIA collection genomes closest to one query using Mash distance.
- DiversiTree — creates a Parsnp or MashTree tree and selects a diverse subset from the supplied genomes.
- dRep — compares assemblies by Mash and secondary ANI algorithms or dereplicates a genome set.
Analyze a pan-genome or microbial association
- Roary/Scoary — calculates a pan-genome and can test binary trait associations against accessory-gene presence/absence.
- GWAS-pyseer — performs microbial genome-wide association with explicit population-structure correction.
Annotate genomes or detect mobile genetic elements
- Prokka — annotates genome assemblies and produces standard feature, nucleotide, and protein outputs.
- MobSuite — reconstructs and types predicted plasmids in draft genome assemblies.
- PHASTEST — identifies, annotates, and visualizes prophage regions in assembled bacterial genomes and plasmids.
Extract or inspect assembly data
- SequenceExtractor — extracts a requested interval or complete contig from an assembly.
- GFA Retrieve — retrieves GFA graphs from supported hybrid assemblies for visualization in Bandage.
Predict protein subcellular localization
- PSORTb — predicts the subcellular localization of proteins encoded by a genome assembly.
Before submitting a request
- Open the selected workflow page.
- Confirm whether it requires raw reads, an assembly, an attachment, or a previous Redmine result.
- Copy the documented Subject exactly.
- Preserve the documented Description order and parameter spelling.
- Review attachment filenames, formats, and size limits.
- Check the expected runtime and troubleshooting section.
Internal operational workflows are intentionally excluded from this standard-access index.