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SUPREMErun  

5 out of 5



SUPREME run is optimised for Sanger sequencing of your individual research samples in tubes or high-throughput sequencing in 96 well plates. Sanger sequencing of plasmids or...
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  • Ease of use 5 out of 5
  • After sales service 5 out of 5
  • Value for money 4 out of 5

89 review(s) of this product / Read All

LIGHTrun  

5 out of 5



LIGHT run is our most convenient and advanced Sanger sequencing solution for your premixed samples.     Sanger sequencing of purified plasmids or PCR fragments ...
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  • Ease of use 5 out of 5
  • After sales service 5 out of 5
  • Value for money 4 out of 5

66 review(s) of this product / Read All

InView™ Microbiome Profiling 2.0  

Highlights: Multiplexing of up to 96 samples Increased amplicon length applying 2 x 300bp paired-end sequencing mode Optimised bioinformatics pipelines for samples of any...
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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 for...
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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 high-quality next...
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Genome Assembly Services  

5 out of 5



We understand that not everyone has the time to invest in assembling, analyzing, and annotating a genome. That's why DNASTAR offers genome assembly and related services using our...
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  • Ease of use 5 out of 5
  • After sales service 5 out of 5
  • Value for money 5 out of 5

1 review(s) of this product / Read All

Lasergene Genomics Suite  

Lasergene Genomics Suite provides all of the software you need for next-gen sequence assembly and analysis in a single, integrated package. We support all major next-gen and third-gen...
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LABWORKS LIMS  

2 out of 5



PerkinElmer has been delivering Laboratory Solutions for over 70 years. As one of the original suppliers of commercial Laboratory Information Management Systems, we understand the important...
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  • Ease of use 4 out of 5
  • After sales service 1 out of 5
  • Value for money 2 out of 5

1 review(s) of this product / Read All

LISA.lims  

LISA.lims, the premier Laboratory Information Management System, helps you to automate, organize, and standardize complex workflows for tracking crucial information required for making...
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Agilent SureCall 2.0 Software  

Agilent SureCall software allows clinical researchers who use NGS panels for inherited diseases and cancer, to analyze, visualize, and contextualize NGS data using a single application. ...
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GeneSpring NGS Software  

Agilent’s GeneSpring NGS software suite includes data analysis workflows for Methyl-Seq, RNA-Seq, DNA-Seq, Chip-Seq and Small RNA-Seq data. GeneSpring NGS provides SureSelect customers with...
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Next Generation Sequencing Services  

PerkinElmer is a NGS service provider you can trust to deliver consistent, high quality next generation sequencing and bioinformatics. We believe that trust is earned, not given.
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HORIZON® LIMS  

3 out of 5



HORIZON is not a do-it-yourself "toolbag" or generic all-purpose LIMS. It's not a converted hospital information system (HIS) or process control LIMS retrofitted for the special needs of...
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  • Ease of use 3 out of 5
  • After sales service 4 out of 5
  • Value for money 4 out of 5

2 review(s) of this product / Read All

CLC Genomics Workbench  

Dominating the high-throughput sequencing data analysis challenge We have overcome the challenge to analyze high-throughput sequencing data faster than it is produced by implementing a...
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Lasergene 12  

DNASTAR Lasergene 12 provides all the software you need for genomics, structural biology, and evolutionary biology research and is available as a complete package or as individual suites...
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InView™ De novo Genome 2.0  

Highlights: Ideal for small genomes Highest N50 fewer and larger contigs Minimum number of mis-assemblies Extremely long reads The cuttinge-edge sequencing...
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InView™ Epigenome  

Highlights: Study your methylome with high-end conversion rate (≤ 99,9%) on true base level resolution Applicable for all organisms with 5-methylcytosines with flexible scaling...
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InView™ Modification Analysis  

Highlights: Resolve strand-specific modifications at single-base resolution Simultaneous detection of sequence and epigenetic variants Hypothesis-free detection InView...
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Variant Analysis  

Identify causal variants from human sequencing data in just hours Rapidly Identify and Prioritize Variants Ingenuity Variant Analysis combines analytical tools and integrated content...
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LV LIMS  

LV LIMS is a comprehensive client server ??ut of the box??Laboratory Information Management System (LIMS) suitable for a wide range of laboratory applications. The easy configuration and...
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LabWare LIMS  

5 out of 5



LabWare LIMS is a full-featured, configurable, enterprise Laboratory Information Management System (LIMS). Our architecture combines the power and security of an enterprise server...
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  • Ease of use 5 out of 5
  • After sales service 5 out of 5
  • Value for money 5 out of 5

2 review(s) of this product / Read All

Ion Reporter™ Software  

Ion Reporter™ Software automates all steps of your bioinformatics pipeline All the steps—from launching the sequencing run to annotating variants—are automated in the Ion Reporter™...
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Oncomine™ NGS Power Tools  

Oncomine™ NGS Power Tools help prioritize therapeutic opportunities with curated NGS data, methods, and an efficient delivery mechanism. They can help to identify and discern driver...
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GeneSifter Lab Edition  

Geospiza's laboratory workflow management system for genetic analysis can simplify laboratory management, increase throughput, reduce errors and support real-time data distribution to...
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OmicsOffice® Software  

OmicsOffice® is a cross-technologies consistent environment that allows the user to rely on the same application for the analysis and integration of data coming from different genomics...
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