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Bulk RNA-seq

Genome-wide transcriptional profiling using bulk RNA sequencing

Bulk RNA sequencing enables quantitative profiling of gene expression across samples, providing a robust view of transcriptional changes associated with biological conditions or experimental perturbations. Standardised workflows support reproducible processing of RNA-seq data, from raw reads through to expression quantification, while maintaining compatibility with widely used downstream analysis approaches.

Careful processing and quality control of RNA-seq datasets allows reliable comparison of expression levels between samples, supporting differential expression analysis, pathway interrogation, and functional interpretation. Re-analysing existing RNA-seq data can extract additional biological insight and ensure results are generated using current best-practice methods without the need for new sequencing.

€ Priced based on project discussion(s). Get in touch:

Details

This service is for the FASTQ data processing, QC reports, and minimal biological or statistical interpretation.

 

Optional add-ons such as figure preparation, or data upload to public repositories, are available on request.

Project Setup
• Includes project discussions and data transfers

Analysis per Sample
• Suitable for 1 to >100 samples

NCBI Submission
• FASTQ FTP upload to generate BioProject and Accession IDs

Figures & Statistics
• Composition, diversity, statistical test, and differential abundance

Video Discussions – n=3
• Kick-off, update, and wrap-up calls

Turnaround Time – 2–3 weeks
• Queue and project size dependent

Delivery – Dropbox / FileZilla
• Data retained for 30 days

Deliverables

All files are shared via secure, GDPR-compliant data transfers.

 

Data upload and release will be organised via Dropbox or Filezilla.

Compute resources are provided by an Irish-based cloud computing provider, CloudCIX

multiqc_report.html
• Aggregated quality control summary of raw and processed sequencing data

aligned_reads
• Processed sequencing reads or transcriptome mappings used for expression estimation

expression_matrix.csv
• Quantitative gene or transcript expression values (rows) per sample (columns)

normalised_expression_matrix.csv
• Normalised expression values suitable for between-sample comparison

sample_qc_metrics.csv
• Per-sample sequencing and mapping statistics

Requirements

Pipelines can be run on (i) newly generated datasets, (ii) publicly available metagenomes, or (iii) a combination of both, enabling comparative analyses across studies and environments.

This flexibility allows integration of novel samples with existing microbiome resources for broader context and reproducibility.

Input Format
• Paired- or single-end FASTQ (gzipped)

Read Length
• 50–150 bp

Depth
• ≥ 3 Mn reads

Optional Preprocessing
• Read repair – BBTools

Accepted Platforms
• Illumina, MGI, Element Biosciences, Ultima Genomics

Technical

All analyses are executed within isolated Conda environments, ensuring full reproducibility and dependency control across runs.

Each tool and database version is tracked, guaranteeing consistent results between projects and over time.

QC
• Tool(s): FastQC v0.12
• Purpose: Per-sample read quality analysis

 

Reporting
• Tool(s): MultiQC v1.31
• Purpose: Combined QC report

 

Trimming
• Tool(s): fastp v0.23
• Purpose: Adapter and low-quality trimming

 

Host Removal
• Tool(s): Kraken2 v2.0.8
• Purpose: Optional; host genome or taxonomy database required

 

Deduplication
• Tool(s): Clumpify v39.33
• Purpose: Duplicate read removal

Read Mapping
• Tool(s): Bowtie2
• Purpose: Short-read mapping to known databases

Workflow

Client data are transferred securely to BioFigR via Dropbox/Filezilla and processed on CloudCIX infrastructure using rsync. All transfers occur within GDPR-compliant environments, with optional deposition to NCBI via FTP only upon client approval. No data are shared or stored beyond the agreed workflow stages.

data_handling.png

Contact BioFigR

This streamlined, reproducible nf-core/rnaseq pipeline ensures data integrity from upload to analysis. BioFigR provides transparent, compliant handling at every stage—so clients can focus on results, not logistics.

Contact BioFigR with the number of samples and reads per sample to receive a quotation, or to discuss project requirements.

Supplementary Info

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