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Lasergene Genomics Suite  
DNASTAR Inc.

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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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SUPREMErun  
GATC Biotech

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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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LIGHTrun  
GATC Biotech

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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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InView™ Microbiome Profiling 2.0  
GATC Biotech

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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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LISA.lims  
Systat Software Inc

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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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Genome Assembly Services  

5 out of 5


DNASTAR Inc.

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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™ Human Exon  
GATC Biotech

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Highlights: Fast access within 10 business days, starting from one sample Applicable for genomic DNA from various sources (tissue, cells, blood and FFPE sample) Special...
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InView™ Transcriptome  
GATC Biotech

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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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LABWORKS LIMS  

2 out of 5


PerkinElmer, Inc.

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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

Agilent SureCall 2.0 Software  
Agilent Technologies

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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 Technologies

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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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HORIZON® LIMS  

3 out of 5


ChemWare, Inc.

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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 3 out of 5
  • Value for money 3 out of 5

2 review(s) of this product / read all

CLC Genomics Workbench  
CLC bio

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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 Inc.

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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  
GATC Biotech

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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  
GATC Biotech

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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  
GATC Biotech

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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  
Ingenuity Systems Inc.

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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  
LabVantage Solutions Inc.

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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

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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 4 out of 5
  • After sales service 5 out of 5
  • Value for money 4 out of 5

2 review(s) of this product / read all

Ion Reporter™ Software  
Life Technologies

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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  
Life Technologies

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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  
PerkinElmer, Inc.

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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  
PerkinElmer, Inc.

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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  
Thermo Fisher Scientific

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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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