The PGTB is an academic platform that makes its skills, expertise and state-of-the-art equipment in the field of genomics available to the public and private scientific community. We support you in carrying out your projects by offering innovative solutions and personalised support.
Our services
SSRseq
Development and genotyping of microsatellite markers using Illumina sequencing
Development and genotyping of all types of species, with or without a reference genome, and on all types of samples, including complex ones (DNA, faeces, etc.)
Metabarcoding
Analysis of 16S, ITS, COI or other regions using Illumina or Oxford Nanopore Technologies sequencing
Illumina: maximum size of 2 × 500 bp and up to 1,152 samples in a single run.
Oxford Nanopore: up to 384 samples per run
Oxford Nanopore: up to 384 samples per run
SNPseq genotyping
Using Illumina sequencing, with characterisation of flanking polymorphisms
95 to 1,140 samples per analysis, across panels of up to 192 SNPs.
Ready to load sequencing
Illumina MiSeq i100 and NextSeq 2000
Delivery time: ~ 4 weeks
Delivery time: ~ 4 weeks
Sequencing of Illumina and custom libraries: WGS, single-cell sequencing, RNA-seq, metabarcoding, metagenomics, etc.
Shotgun sequencing
De novo or resequencing
Short-reads and long-reads
Short-reads and long-reads
Preparation and sequencing of shotgun libraries using Illumina and Oxford Nanopore technologies
DNA capture
Agilent SureSelect chemistry on DNA and methylated DNA
We support you every step of the way, from probe design to data analysis