WHOLE GENOME
Whole-genome sequencing (WGS) yield a complete view of the entire genome. WGS applications are big such as genetic variants in genome-wide association study (GWAS) or marker development program. Indeed, WGS allow us to provide a full profile of single nucleotide polymorphism (SNP) and structural variant, from single insertion/deletion to large structural variant
OUR SERVICES
DNA purity is very important in WGS analysis and we will take a good care of your samples with our state-of-the art DNA extraction process
DNA EXTRACTION
LIBRARY PREPARATION
Library preparation allow us to barcode any of your samples and add sequencing adaptors specific to your favourite platform. Our library preparation is PCR free which will prevent any PCR bias to occur
We have access to a broad range of sequencing platform:
MiSeq | HiSEq | NovaSeq | Ion Torrent
SEQUENCING
BIOINFORMATICS
FAST-GBS pipeline :
- Base calling and demultiplexing
- Alignment to reference sequence
- Quality control and improvement of reads
- Variant calling (SNP, small indels, SVs)