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Vector NTI Advance™ Sequence Analysis Software Dynamic License (Invitrogen™)

The price shown is the list price. To inquire on volume discount or account-specific pricing, please email bioinfosales@invitrogen.com or visit the Vector NTI® Software page.

Dynamic License Server (DLS) is a software installed on-site. It manages the distribution of the purchased number of Dynamic Licenses across purchased Access Seats on the network. Because there are generally more Seats than licenses in the system, not all computers can use the Vector NTI software at the same time. Thus, the number of licenses purchased represents the number of users who can access the Vector application concurrently. For example, an organization may equip 20 computers with 5 Network Licenses, meaning that at most 5 users (at any of the 20 computers) can use the Vector NTI application simultaneously.

Vector NTI Advance™ Sequence Analysis Software Network License (Invitrogen™)

The price shown is the list price. To inquire on volume discount or account-specific pricing, please email bioinfosales@invitrogen.com or visit the Vector NTI® Software page.

Network Licenses are based on the concept of sharing a license among networked computers. All the networked computers (known as “Access Seats") are connected to a designated machine running Invitrogen’s Dynamic License Server (DLS) software. Network Licenses are useful for large groups of users who wish to maximize the number of individual computers that can run a copy of the Vector application.

Sequencing Analysis Software v5.4 Initial License (Applied Biosystems™)

This software enables you to basecall, trim, display, edit, and print data from our entire line of capillary DNA sequencing instruments for data analysis and quality control.

• Obtain longer read lengths, more high-quality bases, and increased accuracy at the 5' end
• Get increased accuracy in regions with low signal-to-noise ratios or with anomalous signal artifacts such as spikes or dye blobs
• Determine the quality of your data using superior metrics from basecalling quality values
• Accelerate quality control using analysis reports with analysis statistics
• Filter out low-quality sequence ends automatically with sequence trimming

Longer Read Lengths with High-Quality Base Pairs
Our significantly improved basecalling algorithm, the KB™ basecaller now gives you up to 100 more high-quality bases than other basecalling algorithms. You also get longer read lengths with high-quality base pairs, mixed basecalling with quality value, and accurate basecalling of usually difficult-to-sequence short PCR fragments.

Easily Review Sequencing Results with Quality Values
This software enables you to customize and color code the range of the quality values to represent low-, medium-, and high-quality bases. This way, when the basecaller identifies each base and assigns it a quality value, all you have to do is look at the color coding to easily review, discard, or accept it. In addition, the software trims the ends of low-quality bases, grays them out on the user interface for easy identification, and calculates a sample score, which is the average quality value for all the bases in the untrimmed region.

Reduce Data Screening Time
Eliminate manual review of sequencing data batches. With the software's Quality Control (QC) reports, you get read length and sample score (average QV of bases in the clear range) for each sample file, enabling you to sort data by quality. And to make reviewing data even easier, each QC report is hyperlinked back to its source data

For Research Use Only. Not for use in diagnostics procedures.

Sequencing Analysis Software v6.0, Initial License (Applied Biosystems™)

This software enables you to basecall, trim, display, edit, and print data from our entire line of capillary DNA sequencing instruments for data analysis and quality control.

• Obtain longer read lengths, more high-quality bases, and increased accuracy at the 5' end
• Get increased accuracy in regions with low signal-to-noise ratios or with anomalous signal artifacts such as spikes or dye blobs
• Determine the quality of your data using superior metrics from basecalling quality values
• Accelerate quality control using analysis reports with analysis statistics
• Filter out low-quality sequence ends automatically with sequence trimming

Longer Read Lengths with High-Quality Base Pairs
Our significantly improved basecalling algorithm, the KB™ basecaller, now gives you up to 100 more high-quality bases than other basecalling algorithms. You also get longer read lengths with high-quality base pairs, mixed basecalling with quality value, and accurate basecalling of usually difficult-to-sequence short PCR fragments.

Easily Review Sequencing Results with Quality Values
This software enables you to customize and color code the range of the quality values to represent low-, medium-, and high-quality bases. This way, when the basecaller identifies each base and assigns it a quality value, all you have to do is look at the color coding to easily review, discard, or accept it. In addition, the software trims the ends of low-quality bases, grays them out on the user interface for easy identification, and calculates a sample score, which is the average quality value for all the bases in the untrimmed region.

Reduce Data Screening Time
Eliminate manual review of sequencing data batches. With the software's Quality Control (QC) reports, you get read length and sample score (average QV of bases in the clear range) for each sample file, enabling you to sort data by quality. And to make reviewing data even easier, each QC report is hyperlinked back to its source data.

Sequencing Analysis Software v7.0, Initial License (Applied Biosystems™)

This software enables you to basecall, trim, display, edit, and print data from our entire line of capillary DNA sequencing instruments for data analysis and quality control.

• Obtain longer read lengths, more high-quality bases, and increased accuracy at the 5' end
• Get increased accuracy in regions with low signal-to-noise ratios or with anomalous signal artifacts such as spikes or dye blobs
• Determine the quality of your data using superior metrics from basecalling quality values
• Accelerate quality control using analysis reports with analysis statistics
• Filter out low-quality sequence ends automatically with sequence trimming

Longer Read Lengths with High-Quality Base Pairs
Our significantly improved basecalling algorithm, the KB basecaller, now gives you up to 100 more high-quality bases than other basecalling algorithms. You also get longer read lengths with high-quality base pairs, mixed basecalling with quality value, and accurate basecalling of usually difficult-to-sequence short PCR fragments.

Easily Review Sequencing Results with Quality Values
This software enables you to customize and color code the range of the quality values to represent low-, medium-, and high-quality bases. This way, when the basecaller identifies each base and assigns it a quality value, all you have to do is look at the color coding to easily review, discard, or accept it. In addition, the software trims the ends of low-quality bases, grays them out on the user interface for easy identification, and calculates a sample score, which is the average quality value for all the bases in the untrimmed region.

Reduce Data Screening Time
Eliminate manual review of sequencing data batches. With the software's Quality Control (QC) reports, you get read length and sample score (average QV of bases in the clear range) for each sample file, enabling you to sort data by quality. And to make reviewing data even easier, each QC report is hyperlinked back to its source data.

GeneMapper™ Software v4.1, full installation (Applied Biosystems™)

GeneMapper® Software is a flexible fragment analysis software package that provides quality DNA sizing and allele calls for all Applied Biosystems® genetic analyzers. This software is designed to support multi-application functionality, including analysis of amplified fragment length polymorphism (AFLP), loss of heterozygosity (LOH), microsatellites, and SNP genotyping.

Features include:
• Multi-user, client-server deployment (through Oracle 11g RDBMS)
• Increased data processing efficiency through remote auto-analysis and command line operation
• Security and audit features to help you meet 21CFR11 requirements
• Organize, manage, and batch-process your data with Report Manager and Database Dashboard
• Automatically evaluate and reduce data review time with Process Quality Values (PQVs) for high-throughput genotyping

The software supports a wide variety of applications on the Applied Biosystems® 3500, 3500xL, 3730, 3730xl, 3130, 3130xl, 3100, 3100–Avant, and 310 instrument systems.

GeneMapper™ Software v4.1, client installation (Applied Biosystems™)

This client version of GeneMapper® Software v4.1 installs the client configuration (user interface) only. Users must install GeneMapper® Software 4.1, full installation, prior to installing the client version, which should be installed on a computer separate from that of the full version.

GeneMapper® Software is a flexible fragment analysis software package that provides quality DNA sizing and allele calls for all Applied Biosystems® genetic analyzers. This software is designed to support multi-application functionality, including analysis of amplified fragment length polymorphism (AFLP), loss of heterozygosity (LOH), microsatellites, and SNP genotyping.

Features include:
• Multi-user, client-server deployment (through Oracle 11g RDBMS)
• Increased data processing efficiency through remote auto-analysis and command line operation
• Security and audit features to help you meet 21CFR11 requirements
• Organize, manage, and batch-process your data with Report Manager and Database Dashboard
• Automatically evaluate and reduce data review time with Process Quality Values (PQVs) for high-throughput genotyping

The software supports a wide variety of applications on the Applied Biosystems® 3500, 3500xL, 3730, 3730xl, 3130, 3130xl, 3100, 3100–Avant, and 310 instrument systems.

GeneMapper™ Software 5, full upgrade (Applied Biosystems™)

This product upgrades a previous Full Installation version of GeneMapper® Software to GeneMapper® Software 5.

GeneMapper® Software is a flexible genotyping software package that provides DNA sizing and quality allele calls for all of our electrophoresis-based genotyping systems. This software specializes in multi-application functionality, including amplified fragment length polymorphism (AFLP®), loss of heterozygosity (LOH), microsatellite and SNP genotyping analysis. GeneMapper® Software can help users increase data processing efficiency with remote auto-analysis and command line operation, and allows for multiuser, client-server deployment. The software uses Process Quality Values (PQVs) for automated identification that reduces data review time for high throughput genotyping. In addition, the security and audit features help users meet 21 CFR 11 requirements.

Features include:

• Installation on the data collection computer or a non-instrument computer
• Support of networked multiple clients when installed on a non-instrument computer
• An Oracle® 11g database with project-related data storage that ensures faster installation times and latest database support, as well as flexible archive capabilities
• Customizable project auto-saving frequency
• Defining of linearity range in the analysis methods for more reproducible, higher quality sizing of larger fragments (>800bps)
• Analysis of 6-dye data generated from the Applied Biosystems® 3500 and 3500xL instrument systems for higher multiplexing capabilities

GeneMapper® Software has not undergone specific developmental validation for human identification applications. Human identification laboratories analyzing single-source or parentage samples that choose to use GeneMapper® Software for data analysis should perform their own developmental validation studies.

Several users may access the database concurrently; however, because genotype analysis is data-intensive, more than five clients simultaneously accessing the database may slow the performance of GeneMapper® Software.

Recommended Computer Configuration: Dell® Optiplex XE, with Core 2 Duo E8400/3.0GHz, 6MB, 1333FSB, 4GB, Non-ECC, 1333MHz DDR3, 2X2GB, Dell OptiPlex 580, 2 x 500GB SATA 3.0Gb/s and 8MB Data Burst Cache, 16X DVD+/-RW SATA, Data Only, 17-inch Color Monitor (1280 x 1024 pixels or higher). Supported Operating Systems: Windows® 7 Professional Service Pack 1 32-bit.

MicroSEQ™ ID Microbial Identification Software v2.0 (Applied Biosystems™)

This easy-to-use software enables you to identify and classify unidentified bacterial or fungal sequences by comparing them to a validated microbial library.

• A validated library of over 2300 microbial sequences help ensure you get the answers you need
• Automatically identify unknown specimens
• Run plates on Applied Biosystems® 3500 Series Genetic Analyzers directly via the MicroSEQ® ID Software
• MicroSEQ® system is a complete integrated solution, including security, audit, and e-signature features
• Qualification and validation support

Confidently Identify Microbes
The MicroSEQ® system comprises bacterial libraries of 500 bp sequences and over 2300 validated entries--including extensive coverage of gram-negative nonfermenters, Bacillus, Coryneforms, Mycobacteria, and Staphylococcus. Another library containing more than 1100 entries is available for fungal identification. To help ensure accurate identification of the species of your sequences, we rigorously validate all library entries. And unlike other widely available databases, MicroSEQ® libraries contain only correctly identified organisms and quality-controlled sequences derived from type strains of preeminent culture collections. The libraries also support sequence polymorphisms, and include bacterial Category A biothreat agents.

Automatically Identify Unknown Specimens
Reviewing each specimen in a project file to make a manual identification call can be tedious and time consuming. The new Auto-ID feature in MicroSEQ® ID Software v3.0 uses a set of editable parameters to automatically identify unknown specimens. The results table is displayed in the report, and an editable comments field allows additional information or manual identifications to be entered into the same table.

Run Plates on 3500/3500xL Instruments Directly via the MicroSEQ® ID Software
Applied Biosystems® 3500 Series Genetic Analyzer users are now able to run plates on these instruments directly via the MicroSEQ® ID Software v3.0 user interface, without needing Autoanalysis Manager. A single software wizard enables you to set up projects, specimens, and plates; adjust the plate layout via drag and drop; start and monitor the run; and review results.

The MicroSEQ® System: A Complete, Integrated Solution
Streamlining every step in microbial identification, the Applied Biosystems® MicroSEQ® system combines the advantages of MicroSEQ® ID Software with easy to use PrepMan® Ultra sample preparation reagents and protocols, MicroSEQ® bacterial and fungal application kits, and industry-leading thermal cyclers and sequencing systems. To help ensure optimal performance and system-wide integration, we develop and test all components of the system together. The MicroSEQ® ID Software also includes security, audit, and electronic signature features enabling the software to smoothly integrate into your workflow.

Qualification and Validation Support
To help ensure seamless integration into your laboratory, from installation to routine operation, we offer comprehensive installation and operational qualification (IQ/OQ) and validation support services.

For Research Use Only. Not for use in diagnostics procedures.

Partek® Flow® Lab Edition Software, 12 Month License (Academic) (Ion Torrent™)

Partek® Flow® Lab Edition provides small labs and departments the tools needed to store, manage, and collaboratively analyze large genomic data sets. Whether a cloud, cluster, or server deployment, it provides the computing resources and flexibility to scale with ever-changing needs.

Partek® Flow® Lab Edition Software, 12 Month License (Commercial) (Ion Torrent™)

Partek® Flow® Lab Edition provides small labs and departments the tools needed to store, manage, and collaboratively analyze large genomic data sets. Whether a cloud, cluster, or server deployment, it provides the computing resources and flexibility to scale with ever-changing needs.

GeneMapper™ Software 5, client upgrade (Applied Biosystems™)

This product upgrades a previous Client Installation of GeneMapper® Software to GeneMapper® Software 5.

GeneMapper® Software is a flexible genotyping software package that provides DNA sizing and quality allele calls for all of our electrophoresis-based genotyping systems. This software specializes in multi-application functionality, including amplified fragment length polymorphism (AFLP®), loss of heterozygosity (LOH), microsatellite and SNP genotyping analysis. GeneMapper® Software can help users increase data processing efficiency with remote auto-analysis and command line operation, and allows for multiuser, client-server deployment. The software uses Process Quality Values (PQVs) for automated identification that reduces data review time for high throughput genotyping. In addition, the security and audit features help users meet 21 CFR 11 requirements.

Features include:

• Installation on the data collection computer or a non-instrument computer
• Support of networked multiple clients when installed on a non-instrument computer
• An Oracle® 11g database with project-related data storage that ensures faster installation times and latest database support, as well as flexible archive capabilities
• Customizable project auto-saving frequency
• Defining of linearity range in the analysis methods for more reproducible, higher quality sizing of larger fragments (>800bps)
• Analysis of 6-dye data generated from the Applied Biosystems® 3500 and 3500xL instrument systems for higher multiplexing capabilities

GeneMapper® Software has not undergone specific developmental validation for human identification applications. Human identification laboratories analyzing single-source or parentage samples that choose to use GeneMapper® Software for data analysis should perform their own developmental validation studies.

Several users may access the database concurrently; however, because genotype analysis is data-intensive, more than five clients simultaneously accessing the database may slow the performance of GeneMapper® Software.

Recommended Computer Configuration: Dell® Optiplex XE, with Core 2 Duo E8400/3.0GHz, 6MB, 1333FSB, 4GB, Non-ECC, 1333MHz DDR3, 2X2GB, Dell OptiPlex 580, 2 x 500GB SATA 3.0Gb/s and 8MB Data Burst Cache, 16X DVD+/-RW SATA, Data Only, 17-inch Color Monitor (1280 x 1024 pixels or higher). Supported Operating Systems: Windows® 7 Professional Service Pack 1 32-bit.

Partek® Flow® Enterprise Edition Software, 12 Month License (Commercial) (Ion Torrent™)

Partek® Flow® Enterprise Edition provides organizations with diverse needs and geographic locations the tools needed to store, manage, and collaboratively analyze large genomic data sets. Whether a cloud, cluster, or server deployment, it provides the elastic computing resources and flexibility to scale with ever-changing needs.

GeneMapper™ Software 5, client installation (Applied Biosystems™)

This client version of GeneMapper® Software 5 installs the client configuration (user interface) only. Users must install GeneMapper® Software 5, full installation, prior to installing the client version, which should be installed on a computer separate from that of the full version.

GeneMapper® Software is a flexible genotyping software package that provides DNA sizing and quality allele calls for all Life Technologies® electrophoresis-based genotyping systems. This software specializes in multi-application functionality, including amplified fragment length polymorphism (AFLP®), loss of heterozygosity (LOH), microsatellite and SNP genotyping analysis. GeneMapper® Software can help users increase data processing efficiency with remote auto-analysis and command line operation, and allows for multiuser, client-server deployment. The software uses Process Quality Values (PQVs) for automated identification that reduces data review time for high throughput genotyping. In addition, the security and audit features help users meet 21 CFR 11 requirements.

Features include:

• Installation on the data collection computer or a non-instrument computer
• Support of networked multiple clients when installed on a non-instrument computer
• An Oracle® 11g database with project-related data storage that ensures faster installation times and latest database support, as well as flexible archive capabilities
• Customizable project auto-saving frequency
• Defining of linearity range in the analysis methods for more reproducible, higher quality sizing of larger fragments (>800bps)
• Analysis of 6-dye data generated from the Applied Biosystems® 3500 and 3500xL instrument systems for higher multiplexing capabilities

GeneMapper® Software has not undergone specific developmental validation for human identification applications. Human identification laboratories analyzing single-source or parentage samples that choose to use GeneMapper® Software for data analysis should perform their own developmental validation studies.

Several users may access the database concurrently; however, because genotype analysis is data-intensive, more than five clients simultaneously accessing the database may slow the performance of GeneMapper® Software.

Recommended Computer Configuration: Dell® Optiplex XE, with Core 2 Duo E8400/3.0GHz, 6MB, 1333FSB, 4GB, Non-ECC, 1333MHz DDR3, 2X2GB, Dell OptiPlex 580, 2 x 500GB SATA 3.0Gb/s and 8MB Data Burst Cache, 16X DVD+/-RW SATA, Data Only, 17-inch Color Monitor (1280 x 1024 pixels or higher). Supported Operating Systems: Windows® 7 Professional Service Pack 1 32-bit.

Partek® Genomics Suite® Software, 12 Month License (Government)

Partek® Flow® Enterprise Edition provides organizations with diverse needs and geographic locations the tools needed to store, manage, and collaboratively analyze large genomic data sets. Whether a cloud, cluster, or server deployment, it provides the elastic computing resources and flexibility to scale with ever-changing needs.