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Lasergene Genomics Suite  

Lasergene Genomics Suite keeps it simple, providing all the software you need for next-gen sequence assembly and analysis, in a single integrated package. We support all major NGS...
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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...
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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

130 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 Premixed...
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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

105 review(s) of this product / Read All

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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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

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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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  

5 out of 5



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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  • Ease of use 5 out of 5
  • After sales service 5 out of 5
  • Value for money 5 out of 5

9 review(s) of this product / Read All

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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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...
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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 ...
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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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DeNovox Automated De Novo Sequencing Software  

DeNovoX software automates and accelerates sequencing, returning results equal to or better than those formerly achieved through expert manual sequencing of peptides within proteins and is...
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