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Next Generation Sequencing Service  

4 out of 5



High throughput sequencing powered by innovation & expertise. Next generation sequencing is not only deep sequencing but also data analysis and project consulting. Eurofins...
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  • Ease of use 5 out of 5
  • After sales service 4 out of 5
  • Value for money 4 out of 5

6 review(s) of this product / Read All

Source BioScience Next Generation Sequencing  

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...
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INVIEW™ Microbiome  

Highlights: 2 x 300bp paired-end sequencing, multiplexing of up 96 samples (Illumina) full-length 16S gene sequencing, multiplexing of up to 10 samples (PacBio) ...
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INVIEW™ Human Exome  

Highlights: Fastest exome sequencing, starting from one sample Applicable for genomic DNA from various sources (tissue, cells, blood and FFPE sample) Special protocol...
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INVIEW™ Transcriptome  

Highlights: Highly standardised Scaled to fit any application and need Guaranteed output of read numbers per package INVIEW ™ stands for streamlined...
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SPRIworks Fragment Library System I for Illumina...  

Fully Automated Fragment Library System for the Illumina* Genome Analyzer The emergence of second generation sequencing technologies has enabled scientists to generate vastly increased...
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Normalized cDNA libraries  

Our cDNA libraries feature full-length-enriched and high quality size-fractionated cDNA. cDNA library construction is usually done in slightly-modified versions of pBluescript or pcDNA3.1.
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Uncloned Normalized cDNA for Next-Generation Seq...  

Our uncloned normalized cDNA is created using proprietary technology which features full-length-enriched and high quality size-fractionated cDNA. Our cDNA has been used successfully with...
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NGSgrade Oligos: Improve Your NGS Data  

NGSgrade oligos are perfectly suited for the demands of any NGS application on all types of instruments (e.g. Illumina HiSeq, Illumina MiSeq, IonProton). The NGSgrade process is derived...
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Accel-NGS™ 1S DNA Library Kit for Illumina  

For the Preparation of DNA Libraries for Next Generation Sequencing (NGS) on Illumina Platforms. Based on innovative Swift technology, the Accel-NGS 1S DNA Library Kit for Illumina...
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Accel-NGS™ 2S DNA Library Kit for Illumina  

For the Preparation of DNA Libraries for Next Generation Sequencing (NGS) on Illumina Platforms. The new Accel-NGS 2S DNA Library Kit for Illumina utilizes a proprietary adapter...
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Accel-NGS™ 2S XT Compatibility Module  

Adapter and pre-hyb PCR primers for preparing DNA libraries for SureSelectXT hybridization and sequencing on the Illumina system.
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Accel-NGS™ DNA Library Kit for Ion Torrent  

For the Preparation of DNA Libraries for Next Generation Sequencing (NGS) on Ion Torrent Platforms. Based on innovative Swift technology, the Accel-NGS DNA Library Kit for Ion Torrent...
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HaloPlex Custom Kits  

HaloPlex custom kits provide you the flexibility to perform pilot studies and easily increase your throughput. Scale up to 96 samples prepped in less than a day with Agilent automation. •...
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SureSelect Custom DNA  

Agilent’s market leading SureSelect platform provides a complete portfolio of catalog and custom products, providing the flexibility you need from discovery to follow-up studies. Agilent’s...
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SureSelect Custom RNA  

Agilent’s market leading SureSelect platform provides a complete portfolio of catalog and custom products, providing the flexibility you need from discovery to follow-up studies. Agilent’s...
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SureSelect DNA Capture Arrays   

Designed for smaller studies, the SureSelect DNA Capture Arrays complement Agilent's in-solution SureSelect Target Enrichment System, which is designed for medium to large-scale NGS studies...
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SureSelect DNA Panels  

Agilent SureSelect DNA panels are predefined designs which focus on targeted gene sets for specific applications. Agilent offers two human panels, the SureSelect Human Kinome panel and...
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SureSelect Focused Exome  

The SureSelect Focused Exome is a highly targeted design that enables analysis of only the disease-associated targets providing deep coverage even on a benchtop sequencer. This design...
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SureSelect Strand Specific RNA Library Preparati...  

Agilent's SureSelect Strand Specific RNA Library Preparation Kit is the highest sensitivity, strand-specific method for preparing libraries for mRNA or targeted RNA-seq, enabling a greater...
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SureSelect Target Enrichment System Kit  

Agilent's SureSelect market leading platform provides a complete portfolio of catalog and custom products, providing the flexibility you need, for your discovery to follow-up studies. ...
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SPRIworks Fragment Library System II for Roche G...  

Fully Automated Fragment Library System for the Roche* 454 GS FLX DNA Sequencer The emergence of next generation sequencing technologies has enabled scientists to generate vastly...
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SPRIworks Fragment Library System III for Life T...  

Fully Automated Fragment Library System for the Life Technologies SOLiD* Sequencer The SPRIworks Fragment Library Systems have built-in size selection and prepare fragment libraries...
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Magna ChIP-Seq™ Chromatin Immunoprecipitation an...  

ChIP-Seq facilitates genome-wide profiling of the interactions of transcription factors, modified histones, and other chromatin associated proteins. By combining chromatin...
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GeneRead DNAseq Library Quant Array  

PCR Array format for QC of target enrichment process and quantification of DNA library in GeneRead DNAseq Gene Panel application QIAGEN Product Finder QIAGEN Online shopping guide
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