Whole Genome Sequencing
Whole Exome Sequencing
Clinical Exome Sequencing
Whole-genome Bisulfite Sequencing
Total RNA-Seq with Ribosomal Reduction
Small RNA Sequencing
ISO-SEQ on PacBio Sequel
16s/18s/ITS Amplicon sequencing
Infinium® Global Screening Array
Illumina Whole-Genome for Livestock
Comprehensive Panel for Solid Tumors
Non-Small Cell Lung Cancer (NSCLC) Panel
Colorectal Cancer (CRC) Panel
PARP inhibitor for Breast & Ovarian Cancers
Application & Services
Nucleic Acid Extraction Services
DNA Genetic Testing
Sanger sequencing is widely used to get high quality long read (up to 500 bp or more) targeting smaller genomic regions in a larger number of samples.
BioXplore offers a wide range of services for Sanger Sequencing to match your project needs.
Sequencing PCR products and plasmid sequences, inserts, mutations.
Sequencing of variable regions
Validating results from next-generation sequencing (NGS) studies
Genotyping of microsatellite markers
Identifying single disease-causing genetic variant