Data Pre-processing
We check the quality of raw reads and prepare them for downstream analysis.
- Quality filtering
- Adapter trimming
- Discarding rRNA-mapped reads or contaminants
- Quality report (HTML/PDF)
- Filtered reads in FASTQ format
From data to biology. Professional analysis of biological data.
We offer a wide array of bioinformatic services for model and non-model organisms
We check the quality of raw reads and prepare them for downstream analysis.
See steps and outputs → RNA-SeqWe estimate gene and transcript expression, then compare it between conditions.
Service details → RNA-SeqWe assemble the transcriptome against a reference genome to detect novel genes and splicing isoforms. On request we also annotate the assembled transcriptome.
See steps and outputs → RNA-SeqWe assemble the transcriptome without a reference, so no genome sequence is needed. On request we add annotation: identification of homologous proteins and long non-coding RNAs.
AnnotationWe identify protein-coding genes and ncRNAs, assign GO terms and KEGG pathways, and identify domains.
See steps and outputs → Small RNAWe identify and quantify miRNAs and siRNAs, and predict their target genes.
Service details → ProteomicsWe analyse mass spectrometry data — from sample preparation support to biological interpretation.
See steps and outputs → GenomicsWe detect SNPs, short indels and structural variants in sequencing data.
Service details → GenomicsWe assemble and annotate bacterial genomes, reaching a closed chromosome with its plasmids, and screen for resistance and virulence genes.
Service details → GenomicsWe assemble plant, animal and fungal genomes from long reads, order them with Hi-C data and annotate genes using RNA-Seq.
Service details → Other NGSWe analyse ChIP-Seq data, study RNA editing and alternative splicing, and deposit data in public repositories.
See steps and outputs → InfrastructureWe provide a ready-to-use computing environment with the software installed, for when you prefer to analyse the data yourself.
See steps and outputs → InfrastructureWe build dedicated pipelines, web applications and biological databases for a specific research project.
See steps and outputs → DesignWe design custom PCR/qPCR primers and probes, and validate their specificity.
We check the quality of raw reads and prepare them for downstream analysis.
We estimate gene and transcript expression, then compare it between conditions.
We assemble the transcriptome against a reference genome to detect novel genes and splicing isoforms. On request we also annotate the assembled transcriptome.
We assemble the transcriptome without a reference, so no genome sequence is needed. On request we add annotation: identification of homologous proteins and long non-coding RNAs.
We identify protein-coding genes and ncRNAs, assign GO terms and KEGG pathways, and identify domains.
We identify and quantify miRNAs and siRNAs, and predict their target genes.
We analyse mass spectrometry data — from sample preparation support to biological interpretation.
We detect SNPs, short indels and structural variants in sequencing data.
We assemble and annotate bacterial genomes, reaching a closed chromosome with its plasmids, and screen for resistance and virulence genes.
We assemble plant, animal and fungal genomes from long reads, order them with Hi-C data and annotate genes using RNA-Seq.
We analyse ChIP-Seq data, study RNA editing and alternative splicing, and deposit data in public repositories.
We provide a ready-to-use computing environment with the software installed, for when you prefer to analyse the data yourself.
We build dedicated pipelines, web applications and biological databases for a specific research project.
We design custom PCR/qPCR primers and probes, and validate their specificity.
Tell us what you are working on. Discussing the project and quoting it are free of charge, and we will help you pick the right analysis.
Get in Touch