Transcriptome Profiling Package
Revealing gene expression, decoding biological mechanisms

3
Analysis Levels Covered
95%
Sequencing reads aligned to the reference transcriptome
100%
Workflow compatible with RNA-seq, RT-qPCR, dPCR, and downstream validation
Our Transcriptomic Profiling Plans
Packages (Standard):
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Bulk RNA-seq (total RNA, mRNA, miRNA)
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Metatranscriptomics
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Gene expression by RT-qPCR (relative quantification)
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Gene expression by digital PCR (absolute quantification)
Projects (Custom):
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Single-cell RNA-seq (scRNA-seq)
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Spatial transcriptomics
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Exosome / extracellular RNA (cfRNA, exosomal RNA)
Why Choose Our Transcriptomic Packages?
✅ Personalized approach tailored to your samples and objectives
✅ End-to-end expertise from extraction to interpretation
✅ Proven flexibility in both technology and analysis
✅ A scientific partnership, not just a service
Decoding gene expression to unlock biological complexity
Deciphering molecular mechanisms through in-depth gene expression analysis
Le profilage transcriptomique permet d’analyser l’expression des gènes afin de mieux comprendre les processus biologiques sous-jacents, qu’il s’agisse de la régulation de voies métaboliques, des réponses à des traitements ou de l’identification de biomarqueurs spécifiques.
Chez GENXMAP, nous vous accompagnons dans cette démarche avec des solutions adaptées à vos enjeux scientifiques, que vous soyez en recherche fondamentale, en biotechnologie ou en médecine personnalisée.
Explorer le transcriptome dans toute sa richesse, du bulk RNA-seq à la transcriptomique spatiale
We offer a global and exploratory approach to the transcriptome, ideal for biomarker discovery, molecular signature characterization, or the analysis of cellular states:
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Bulk RNA sequencing: total RNA, mRNA, or miRNA — providing expression profiles at the sample level
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Single-cell RNA-seq: cell-resolution analysis to decipher heterogeneity with in complex populations
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Spatial transcriptomics: preserving tissue architecture to understand the topographic organization of gene expression
Precise quantification, validation, and detection of specific transcripts
We also offer a targeted approach for the validation of exploratory results or the study of specific genes of interest
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RT-qPCR: relative quantification of a transcript panel with high sensitivity
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Digital PCR: ultra-sensitive detection of rare or low-abundance transcripts, with the possibility of absolute quantification
A global approach with an integrated, optimized process
End-to-end turnkey approach with personalized guidance, from nucleic acid purification to data interpretation
1. RNA Extraction
Obtain high-quality RNA extracts, essential for your transcriptomic analyses
Applications:
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Extraction of RNA (total RNA, mRNA, and miRNA) from diverse matrices (cell cultures, tissues, blood, biofilms, etc.)
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Verification of RNA quality and concentration prior to RNA-seq, qPCR, or targeted transcriptomic analyses
Techniques:
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Optimized extraction kits with protocols adapted to sample type and analytical objectives, including purification steps and removal of residual genomic DNA
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Nanodrop: rapid measurement of RNA concentration and purity (260/280 and 260/230 ratios)
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Qubit: sensitive and precise quantification of total RNA, including low-concentration samples
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Fragment Analyzer / TapeStation: assessment of RNA integrity (RIN/RQN), essential for RNA-seq and transcriptomic applications
2. Library Preparation and Quality Control
Prepare your RNA-seq libraries and ensure their quality for high-performance sequencing
Applications:
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Preparation of samples for RNA-seq sequencing
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Global or targeted transcriptomic analyses
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Differential gene expression studies
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Identification of novel transcripts
Techniques:
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Library preparation kits adapted to RNA type (total RNA, polyA+, messenger RNA, or small RNAs) and study requirements
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Fragment Analyzer / TapeStation: verification of library size and quality, detection of potential dimers or abnormal profiles
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Qubit: precise quantification of libraries prior to sequencing
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Library-specific qPCR: functional quantification of sequencing-ready libraries, ensuring optimal yield and homogeneous coverage
3. Next-Generation Sequencing (NGS)
Perform your RNA-seq sequencing with rigorous quality control and actionable results
Applications:
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Sequencing of total RNA, polyA+ RNA, or small RNAs
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Differential expression analyses
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Identification of novel transcripts
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Transcriptomic profiling across different species and experimental conditions
Techniques:
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NovaSeq 6000 (Illumina): platform tailored for transcriptomic projects
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Paired-end sequencing (2×100 bp or 2×150 bp) with sequencing depth adjusted to study objectives (20 to 100 million reads per sample)
4. Bioinformatics & Biostatistics
Leverage your sequencing data with our tailored bioinformatics and biostatistics analyses
Applications:
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Processing and analysis of NGS data
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Identification of genes or signaling pathways of interest
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Differential expression analyses
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Clustering and functional interpretation
Techniques:
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Read quality control of raw sequencing data (FastQC) and adapter/quality trimming.
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Alignment to the reference genome.
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Expression quantification (delivery of a normalized count matrix )
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Differential expression (DEGs): identification using DESeq2/edgeR with outputs including log2 fold change and adjusted p-values.
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Functional annotation & pathway enrichment (GO, KEGG, Reactome).
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Exploratory analysis & visualization: PCA, heatmaps, clustering, custom figures and reports.
Our Ready-to-Use Packages
Optimized, ready-to-use workflows...
Our solutions, your project!
Check our shop for pricing and ordering options.
*For any order ≥ 24 samples
Proposed Configuration
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Target: Complete transcriptome (polyA mRNA)
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Samples: Cells, tissues, biopsies, biological fluids
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Methodology:
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QC: RNA quantification (Qubit), integrity check (Bioanalyzer/Tapestation RIN ≥7), genomic DNA removal
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Total RNA: library preparation with poly(A) selection
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Sequencing: Illumina (2×100 bp, ~20M reads/sample)
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Bioinformatics: QC and primary analysis → differential analysis → results integration → network analysis → synthesis & final reporting with publication-ready visualizations
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Deliverables: FASTQ & BAM/BAI files + count matrices (CSV/XLSX) + differential results & enrichment analyses (XLSX) + reports and result visualizations
Options: Microfluidic or plate-based partitioning; deep sequencing; fusion/splicing detection; clinical or multi-omics co-analysis; ribodepletion; specialized kits for low RNA integrity or low-/ultra-low input RNA.
Check our shop for pricing and ordering options.
*For any order ≥ 48 samples
Proposed Configuration
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Target: Total microbial RNA (expressed mRNA, rRNA-depleted)
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Samples: Active microbiota (gut, skin, soils, biofilms)
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Methodology:
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Microbial RNA extraction
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Post-extraction quality control (quantity, purity, integrity; RIN ≥7)
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rRNA depletion
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RNA-seq library preparation
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Sequencing: Illumina NovaSeq 6000 (2×100 bp, ~20M reads/sample)
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Bioinformatics: QC/filtering → microbial transcriptome assembly → functional annotation → expressed gene quantification → active metabolic pathway analysis → result visualization
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Deliverables: FASTQ files + QC reports; gene/pathway expression matrices; functional profiles (heatmaps, PCoA, enrichment analyses); PDF summary report
Options: Multi-omics integration (DNA + RNA); increased sequencing depth; differential analyses (treatment response, experimental conditions); post-analysis meeting (60 min) for results presentation and discussion
Check our shop for pricing and ordering options.
*For any order ≥ 48 samples
Proposed Configuration
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Target: Targeted expression (genes of interest + reference genes)
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Samples: Total RNA from cells, tissues, or fluids
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Methodology:
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QC: purity (A260/280), absence of genomic DNA
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RT: cDNA synthesis
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qPCR: TaqMan (ΔΔCt method)
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Analysis: Normalization to housekeeping genes → calculation of relative variation → visualizations
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Deliverables: Ct tables + relative expression ratios + PDF report
Options: Independent validation by RNA-seq; TaqMan multiplex; reference gene stability analysis; SYBR Green chemistry
Check our shop for pricing and ordering options.
*For any order ≥ 48 samples
Proposed Configuration
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Target: Targeted expression (genes of interest + reference genes)
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Samples: Total RNA from cells, tissues, or fluids
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Methodology:
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QC: purity (A260/280), absence of genomic DNA
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RT: cDNA synthesis
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dPCR: TaqMan (absolute quantification method)
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Analysis: Positive/negative counting → estimation of absolute concentration → calculation of target ratios
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Deliverables: Absolute values (copies/µL) + tables + quantification charts + PDF report
Options: Rare mutation detection; clinical biomarker validation; target multiplexing
Our solutions
Precise and advanced services, cutting-edge technologies, and reliable analyses.
Our rigorous approach ensures detailed results, essential for your scientific discoveries and clinical applications.











