About Us
Products
Genomic Solutions
Genomic Sequencing
Whole Genome Sequencing
Whole Exome Sequencing
Clinical Exome Sequencing
Whole-genome Bisulfite Sequencing
ChIP-seq
Gene Regulation
Total RNA-Seq with Ribosomal Reduction
Small RNA Sequencing
mRNA Sequencing
Dual RNA-seq
ISO-SEQ on PacBio Sequel
Microbial Sequencing
Microbial WGS
16s/18s/ITS Amplicon sequencing
Metagenomics
SNP Genotyping
GeneChiP Axiom
PMRA
PMDA
Illumina array
Infinium® Global Screening Array
Illumina Whole-Genome for Livestock
Molecular Karyotyping
Clinical Oncology
Comprehensive Panel for Solid Tumors
Non-Small Cell Lung Cancer (NSCLC) Panel
Colorectal Cancer (CRC) Panel
PARP inhibitor for Breast & Ovarian Cancers
Application & Services
Sanger Sequencing
Nucleic Acid Extraction Services
Bioinformatics
Agri-Seq
ddRAD
GWAS
DNA Genetic Testing
PrediKT
OncoSx
Partnerships
Contact Us
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Sanger Sequencing
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
HLA typing
Genotyping of microsatellite markers
Identifying single disease-causing genetic variant