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.
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.
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.
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.