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Genomic Solutions

BioXplore is offering and tailoring most types of
Genomic services for development needs. 

Whole Genome Sequencing


BioXplore’s Whole Genome Sequencing (WGS) provides the most comprehensive map of an organism's genetic make-up, which covers all corners of an organisms’ entire genome.

Whole genome sequencing for interrogating single-nucleotide variants (SNVs), insertions and deletions (indels), structural variants (SVs), and copy number variants (CNVs) in coding and non-coding regions of the genome.

Whole-Exome Sequencing


BioXplore employs the Illumina system to provide the fast and accurate whole exome sequencing. The exome represents less than 2% of the human genome but contains about 85% of known disease-causing variants.

BioXplore offers exome sequencing services for a wide variety of species, sample types like FFPE, Serum or Plasma, Frozen Tissue, Whole blood and many other sample types including PBMCs, flow-sorted cells, plant tissue etc.  

Clinical Exome Sequencing


Custom targeted sequencing is designed to isolate and deep-sequence a specific region of the genome. Targeted sequencing includes methods such as gene panels where regions or genes of interest are amplified and sequenced.

Whole-genome Bisulfite Sequencing


As a leading provider of NGS services, BioXplore is providing an integrated portfolio of methylation sequencing services.

Whole-genome bisulfite sequencing (WGBS) or bisulfite sequencing (Bisulfite-Seq or BS-Seq) combines bisulfite treatment with next-generation sequencing (NGS) for epigenetic analysis of the methylome of nearly any organism with single-base resolution.



BioXplore offer ChIP-Seq to investigate any protein of interest and locate potential binding sites in the entire genome of a specific organism.

ChIP-Seq combines chromatin immunoprecipitation (ChIP) with next-generation sequencing (NGS) to identify the genomic loci of DNA-protein binding sites.