NGS Services
LGC Diagnostics and Genomics - Rapid Genomics Genotyping SolutionsNext-generation sequencing (NGS) technologies have dramatically reduced sequencing costs and led to novel approaches in many fields of biology.
Next-generation sequencing (NGS) technologies have dramatically reduced sequencing costs and led to novel approaches in many fields of biology.
Our latest generation Ovation RNA-Seq System V2 provides a fast and simple method for preparing amplified cDNA from total RNA for RNA-Seq applications, now with enhanced transcript coverage and uniform distribution of sequencing reads. Amplification is initiated at the 3' end as well as randomly throughout the whole transcriptome in the sample. This feature makes the Ovation RNA-Seq System V2 ideal for amplification prior to…
SURVEYOR Mutation Detection Kits provide a simple, accurate and cost-effective means to scan DNA fragments for mutations with unmatched sensitivity and specificity. The SURVEYOR Mutation Detection Kit for Standard Gel Electrophoresis has been designed to cleave unlabeled DNA fragments at mismatched sites for subsequent analysis by agarose gel electrophoresis or polyacrylamide gel electrophoresis (PAGE). DNA 200 to 4,000 bp lo…
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…
Introducing the next-generation sequencing system for the molecular diagnostic laboratory. The Ion PGM™ Dx Instrument System* will deliver the speed and simplicity of the Ion Torrent™ platform, combined with key workflow advantages designed specifically for regulated laboratory environments and in vitro diagnostic applications. Used in conjunction with Ion PGM™ Dx library kits, Ion One Touch™ Dx template kits,…
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…
DNA library preparation of difficult samples for NGS on Illumina® platforms.
Ion AmpliSeq HD technology is a new amplicon-based library preparation technology for Ion Torrent next-generation sequencing (NGS) that gives you the power to design your own panels and find variants with a low limit of detection—down to 0.1% for cell-free DNA samples. This revolutionary technology enables researchers to routinely get answers when ultrahigh sensitivity is required, such as when detecting low-frequency alleles…
A streamlined solution to convert up to 96 DNA samples to a single, ready-to-sequence 16S library.
Bionano Prep Kits™ provide the critical reagents and protocols needed to extract and label high molecular weight (HMW) DNA for use on the Irys ® and Saphyr™ genome mapping systems. Bionano kits are optimized for performing Bionano genome mapping applications on a variety of sample types.
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.
Accurate and sensitive quantification of DNA, RNA, and protein with flexible throughput
DNA and RNA clean-up for next generation sequencing library construction. 1ml sample is available by request.
The Sanger sequencing services are well-equipped to handle DNA sequencing including single-tube, high-throughput and glycerol DNA sequencing projects
The unique workflow of the NEBNext Small RNA library prep kits addresses the challenge of minimization of adaptor-dimers while achieving production of high-yield, diverse multiplex libraries in a simple protocol.