DNA Sequencing Products & Reviews

Our Mycoplasma Plus PCR Primer Set detects infection by all forms of Mycoplasma with a robust single-band PCR product (triplet for Acholeplasma). This kit also includes controls to verify PCR amplification and Mycoplasma genomic DNA. The primer design permits higher annealing temperatures, reducing spurious bands from PCR contaminants.

The future of NGS library preparation is here. 

The NGS STARlet is a compact, flexible and future-proof workstation for library preparation for all common sequencing platforms. It is excellently suited for any throughput from 8 to 48 samples and reduces time consuming manual pipetting steps and sample-to-sample variability. The open workstation concept allows automation of any library preparation chemistry.

Twist Bioscience, the leader in synthetic DNA with unparalleled precision at scale, is redefining targeted sequencing performance with the Twist Human Core Exome Kit. This kit includes library preparation and enrichment components, allowing the flexibility to lower sequencing costs, increase sample throughput, and achieve a higher depth of coverage across target regions with uncompromising quality.

Positive controls provide quality control measures for the verification and validation for point-of-care diagnostic tests including both next-generation sequencing (NGS) and reverse transcriptase-polymerase chain reaction (RT-PCR) assays. Twist offers fully synthetic SARS-CoV-2 RNA controls, available for dozens of distinct reference sequences.

The mouse is an extremely important model system for studying genetic variation, tumor mutations, and phenotypic outcomes as well as the therapeutic effect of pharmaceutical agents. As genetic variant databases are continuously updated, the Twist Mouse Exome panel is thoughtfully designed and built from the most current databases

The Twist Comprehensive Viral Research Panel covers reference sequences for 3,153 viruses, including 15,488 different strains.

Fosmid clones are similar in size (ca. 40kb) to cosmids, but, like BAC clones, they contain replicons derived from the F factor for DNA replication and segregation. Because of this property, they are present in low copy number and consequently more stable than cosmids. Also, the copy control vector can be used for easy DNA purification from fosmid clones. Fosmid libraries are commonly used for closing gaps in a whole genome se…

The PowerPlex® Fusion System is a 24-locus multiplex for human identification applications including forensic analysis, relationship testing and research use.   The PowerPlex® Fusion System provides all of the materials needed for co-amplification and five-color fluorescent detection of 24 loci (23 STR loci and Amelogenin), including the CODIS core loci and the European Standard Set (ESS) loci. With 24 loci, the sys…

Offering 16-capillary throughput and advanced automation capabilities, the Applied Biosystems 3130xl Genetic Analyzer is ideal for medium-throughput laboratories that need streamlined set-up and 24-hour unattended operation. Run a wide variety of sequencing and fragment analysis applications including microsatellite analysis, AFLP, LOH, SNP validation, and SNP screening. Reduce maintenance time by eliminating manual syringe wa…

Next-generation sequencing (NGS) technologies have dramatically reduced sequencing costs and led to novel approaches in many fields of biology.

SUPREMERUN is optimised for Sanger sequencing of your individual research samples in tubes or 96 well plates. 

LIGHTRUN is our most convenient Sanger sequencing solution for your premixed samples.

Highlights: Fastest exome sequencing, starting from one sample Applicable for genomic DNA from various sources (tissue, cells, blood and FFPE sample) Special protocol for low-input samples (≥ 10ng) Available under diagnostics standard (ISO17025) INVIEW™ stands for streamlined high-quality next generation sequencing (NGS) solutions for specific applications. Exome enrichment with the latest Agilent SureSele…

Source BioScience have over 15 years of sequencing experience and a unique network of state of the art sequencing laboratories meaning we are perfectly placed to be your local provider for sequencing. Source BioScience have a reputation for providing the highest quality data combined with excellent turnaround times. Pre-paid sequencing vouchers are available for purchase which offer both cost and time savings.

Source BioScience are one of Europe’s leading providers of commercial sequencing offering services on the most prominent next generation sequencing platforms including the Illumina MiSeq and HiSeq. Source BioScience's next generation sequencing service is Illumina CSPro accredited and operates through a robust quality management system. Customers benefit from both excellent service and rapid turnaround times. Source BioScienc…

The new Sequel System is based on Pacific Bioscience’s proven Single Molecule, Real-Time (SMRT) technology and delivers about 7X more reads with 1 million zero-mode waveguides (ZMWs) per SMRT Cell. The Sequel System is ideal for projects such as rapidly and cost-effectively generating high-quality whole genome de novo assemblies. This innovative sequencing system features automated reagent and SMRT Cell handling and an inte…

Custom design your oligonucleotide according to your specifications. Our probes and primers are manufactured at unmatched quality under ISO 9001 and 13485 compliance. Whether you need RUO or GMP grade oligos, choose from a vast selection of modifications to customize your oligos for your application.

Exceptional flexibility in next-generation sequencing

An affordable benchtop instrument for Sanger sequencing and fragment analysis.

Saphyr, Bionano’s high-speed, high-throughput genome mapping solution, detects and analyzes genome-wide structural variations with exceptional sensitivity and specificity to reveal the true structure of any genome. Saphyr’s breakthrough speed and throughput combined with unmatched structural variation sensitivity make it the ideal solution for identifying disease-associated structural variants in human genetics and oncology tr…

riboPOOL by siTOOLs Biotech is the market‘s most flexible solution in ribosomal RNA (rRNA) depletion prior to RNA-Seq or other analysis. Achieve efficient and specific rRNA depletion for any species with siTOOL’s proprietary oligo design and high complexity pooling technology. Suitable for metagenomic RNA-Seq and non-polyA-dependent.

STRmix is sophisticated forensic software used to resolve mixed DNA profiles previously considered too complex to interpret.

DNA Sequencing Services

DNA and RNA clean-up for next generation sequencing library construction. 1ml sample is available by request.