Shop All Sequencing & Genetic Analysis Software

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.

Ridom™ SeqSphere+ Software for Ion Torrent™ Systems (Commercial) (Ion Torrent™)

SeqSphere+ Software from Ridom allows for automatic processing and analyzing of microbial sequence data obtained from Ion Torrent™ systems. SeqSphere+ Software enables whole genome microbial typing (MLST+) or traditional MLST sequencing projects. This software is designed both for individual labs and for distributed work-groups (client/server model) to enable easy data sharing. License options are available for 1, 3, or 5 years; 2 or 5 seats; and commercial or academic/government labs.

Ridom SeqSphere+ Software Features:

User-friendly: no scripting skills or bioinformatician needed

Highly automated workflow: download a pre-designed task template or create a custom template, then apply it to the analysis of hundreds of strains with almost no user intervention.

Single, expanding nomenclature service: worldwide, unique nomenclature service that enables a 'Molecular Typing Esperanto'

DNA re-sequencing editor: edit and analyze reference-mapped assemblies of Ion Torrent™ data (e.g., MLST, MLST+) with auto-correction of homopolymer-related insertion/deletion errors.

Sanger data: assemble, edit, and analyze Sanger CE sequencing data (e.g., MLST).

Analytical tools: select data entries from a comparison table for epidemiologic, evolutionary, or functional analysis. Cluster and visualize data entries by using minimum spanning or UPGMA/neighbor-joining trees.

Database:
   --Store, search, retrieve, export, and create reports from your epidemiologic and DNA sequence data stored in an integrated database. Search new sequence entries against stored data.
   --Data fields are compliant with the metadata requirements of the NCBI BioSample. Enables data entry plausibility checks.

Bacterial typing: typing of bacteria is automatically performed with user-defined quality parameters (e.g., coverage, stop codons) using public or self-defined query libraries and task templates.

Ridom Community:
   --Rapidly and easily share task templates with other institutions or download them online from the Task Template 'Store'.
   --Option to contribute to a single, worldwide, expanding, publicly-available database of nomenclature and epidemiologic data. Larger (supra) national institutions may obtain their own server for epidemiologic data upon request.

Security:
   --Encryption (SSL) of data in transmission
   --Various configurable user roles, user groups, and access controls
   --Audit trail functionality (who, when and what)

Computer Specifications (Minimum)

Client computer OS: Windows® 7 64-bit, CPU: Core i5, RAM: 8 GB, HD: 500 GB, Internet connection required to use public Ridom MLST+ Nomenclature Server & Task Template 'Store' (supports working with a private and local nomenclature and to generate custom tasks).

Server computer OS: Windows® 7/Linux 64-bit (Ubuntu LTS recommended), CPU: Core i5, RAM: 8 GB (48 GB recommended if MIRA de novo assembly done on this server), HD: 2 TB (RAID level 1 or 5 recommended), it is recommended not to use the NGS machine computer as server.

MicroSEQ™ ID Microbial Identification Software Lite v3.1 Bundle (Applied Biosystems™)

MicroSEQ ID Microbial Identification Software v3.1 allows you to easily identify and classify unidentified bacterial or fungal sequences by comparing them to a validated microbial library. The Lite version of the software is for use on a stand-alone PC (not connected to the genetic analyzer) for simple analyses. This bundle includes the bacterial and fungal sequence libraries.

• A validated library of over 3000 microbial sequences helps ensure you get the answers you need
• Automatically identify unknown specimens
• The MicroSEQ system is a complete integrated solution, including security, audit, and e-signature features
• Qualification and validation support are available

Confidently identify microbes
The MicroSEQ ID sequence libraries consist of bacterial libraries of 500 bp 16S rDNA sequences and approximately 9300 validated entries, including extensive coverage of gram-negative non-fermenters, Bacillus, Coryneforms, Mycobacteria, and Staphylococcus, as well as a fungal library containing more than 1300 entries. 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 Auto-ID feature in MicroSEQ ID software 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 v3.1 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 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.

Ridom™ SeqSphere+ Software for Ion Torrent™ Systems (Academic/Government) (Ion Torrent™)

SeqSphere+ Software from Ridom allows for automatic processing and analyzing of microbial sequence data obtained from Ion Torrent™ systems. SeqSphere+ Software enables whole genome microbial typing (MLST+) or traditional MLST sequencing projects. This software is designed both for individual labs and for distributed work-groups (client/server model) to enable easy data sharing. License options are available for 1, 3, or 5 years; 2 or 5 seats; and commercial or academic/government labs.

Ridom SeqSphere+ Software Features:

User-friendly: no scripting skills or bioinformatician needed

Highly automated workflow: download a pre-designed task template or create a custom template, then apply it to the analysis of hundreds of strains with almost no user intervention.

Single, expanding nomenclature service: worldwide, unique nomenclature service that enables a 'Molecular Typing Esperanto'

DNA re-sequencing editor: edit and analyze reference-mapped assemblies of Ion Torrent™ data (e.g., MLST, MLST+) with auto-correction of homopolymer-related insertion/deletion errors.

Sanger data: assemble, edit, and analyze Sanger CE sequencing data (e.g., MLST).

Analytical tools: select data entries from a comparison table for epidemiologic, evolutionary, or functional analysis. Cluster and visualize data entries by using minimum spanning or UPGMA/neighbor-joining trees.

Database:
   --Store, search, retrieve, export, and create reports from your epidemiologic and DNA sequence data stored in an integrated database. Search new sequence entries against stored data.
   --Data fields are compliant with the metadata requirements of the NCBI BioSample. Enables data entry plausibility checks.

Bacterial typing: typing of bacteria is automatically performed with user-defined quality parameters (e.g., coverage, stop codons) using public or self-defined query libraries and task templates.

Ridom Community:
   --Rapidly and easily share task templates with other institutions or download them online from the Task Template 'Store'.
   --Option to contribute to a single, worldwide, expanding, publicly-available database of nomenclature and epidemiologic data. Larger (supra) national institutions may obtain their own server for epidemiologic data upon request.

Security:
   --Encryption (SSL) of data in transmission
   --Various configurable user roles, user groups, and access controls
   --Audit trail functionality (who, when and what)

Computer Specifications (Minimum)

Client computer OS: Windows® 7 64-bit, CPU: Core i5, RAM: 8 GB, HD: 500 GB, Internet connection required to use public Ridom MLST+ Nomenclature Server & Task Template 'Store' (supports working with a private and local nomenclature and to generate custom tasks).

Server computer OS: Windows® 7/Linux 64-bit (Ubuntu LTS recommended), CPU: Core i5, RAM: 8 GB (48 GB recommended if MIRA de novo assembly done on this server), HD: 2 TB (RAID level 1 or 5 recommended), it is recommended not to use the NGS machine computer as server.

MicroSEQ™ ID 16S rDNA 500 Supplemental Library (Applied Biosystems™)

The MicroSEQ ID 16S rDNA 500 Supplemental Library is a stand-alone library that extends the size of the MicroSEQ ID 16S rDNA 500 Library v2013 to strengthen the identification process when using MicroSEQ ID Microbial Identification Software. The Supplemental library contains 7,138 16s rDNA public sequences of type and non-type strains of bacterial species that underwent the same rigorous validation process as the sequences in the MicroSEQ ID 16S rDNA 500 Library v2013. The Supplemental Library is used when the MicroSEQ ID 16S rDNA 500 Library v2013 results in a percent match lower than the species ID acceptance criteria.

Key features include:
• Quality controlled—an in-silico validated library with over 7,000 type and non-type strains quality-checked for sequence, taxonomy, nomenclature, and phylogeny
• Simplified—reliable entries from public resources converted into a simple format for routine validation of unique environmental isolates
• Consistent—the same acceptance criteria for analysis and the same reporting format in the software
• Maintained—regular updates for entries and information supported by experienced Thermo Fisher Scientific technical staff

Partek® Flow® Lab Edition Software, 12 Month License (Government) (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.

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.

Ion Reporter™ Server System (Ion Torrent™)

The Ion Reporter Server System is a combined hardware and software solution for analyzing human and bacterial sequencing data. It consists of a locally deployed computer with a suite of informatics tools that streamlines and simplifies analysis, annotation, and archiving of semiconductor sequencing data from any Ion Torrent sequencer. The Ion Reporter Server System combines the ease of use of Ion Reporter Software with the control and access of a powerful computer server in your own building. A locally deployed computer affords many benefits, such as tighter control of the hardware and software versioning. In addition, data uploads from the Torrent Server are faster when the transfer is within your own network. With your own hardware, you have access to unlimited analyses, as well as more options for integration into your lab's workflow.

Streamlined integration with Ion Torrent next-generation sequencing systems
The Ion Reporter Server System is built to complete the next-generation sequencing workflow from sequencing data to report. This platform builds on the sample processing and sequencing output from the Ion S5, Ion S5 XL, Ion PGM, and Ion Proton systems by coupling tightly with the Torrent Server for data transfer and analysis initiation. When a sequencing run is started, an Ion Reporter Software workflow can be pre-designated so the data transfer and analysis are initiated seamlessly, eliminating the hands-on time between run initiation and reviewing annotated variants, with a host of annotations added to guide understanding.

Flexible analyses with controlled pipelines
Many research applications, including applications in the areas of oncology, inherited disease, reproductive health, and 16S bacterial metagenomics, are supported within Ion Reporter Software using pre-tuned, customizable analysis workflows. These workflows can be used to analyze single samples, paired tumor/normal samples, and family trios. Detect germline or somatic SNPs, indels, gene fusions, and CNVs in a single workflow. Use algorithms designed for oncological somatic variant detection, liquid biopsy cfDNA variant detection, and others designed specifically for low-pass whole-genome copy number for aneuploidy detection and inherited disease research applications. The analysis workflows designed around targeted sequencing have been specifically developed for Ion AmpliSeq gene panels and Oncomine assays. Ion Reporter Software also includes a 16S metagenomics workflow, which enables environmental and clinical researchers interested in bacterial populations to identify and classify the relative proportions of microbes present at any taxonomic level from one or multiple mixed populations.

Each of the Ion Reporter Software workflows can be used as pre-configured or modified and then locked for controlled use without the need for an analyst or bioinformatician. Alternatively, the platform is extensible with our software APIs to drive integration with your lab environment and processes. By integrating detected variants with comprehensive public and Ion Torrent proprietary annotations and your own lab-specific content, Ion Reporter Software helps reduce your bioinformatics work and the time needed to interpret your results. The analysis modules and parameters are configurable, allowing you to customize the workflow to fit your research needs. Workflows are open for development and testing, and may be locked for repeated use in an auditable production environment when desired. These features make Ion Reporter Software an ideal solution for clinical researchers needing a simple bioinformatics tool that helps ensure consistency of results.

Workflows follow intuitive steps
The Ion Reporter Software workflow steps mirror the typical role-based sample processing workflow used by most labs. Sequencing reads from Ion S5, Ion S5 XL, Ion PGM, or Ion Proton systems are automatically imported from the Torrent Browser into the local Ion Reporter Software environment for read mapping, variant detection, multi-sample analysis, and annotation. You can then filter the identified variants based on technical criteria such as read coverage, P-value, allele frequency, and a growing set of annotations such as gene names, conservation scores, COSMIC, OMIM and other public and proprietary classifications. After you classify and interpret the variants, Ion Reporter Software displays this summary in an easily readable report alongside the relevant variants and their corresponding annotations.

Ion Reporter Software can also be used for long-term data management and access to individual files and audit logs. The computer server enables Ion Reporter Software to provide scalable analysis and control of your data and results. In addition, the software is designed to the same robust data security standards as described in the HIPAA implementation guidelines.

Services and support
Service and support plans—comprehensive plans to maximize instrument performance and ensure availability of critical systems
Training—courses for experimental design, data analysis, troubleshooting, applications, and instrument operation
Bioinformatics—tailored support for NGS informatics execution, software use, data analysis, and downstream applications
DataSafe Solution—storage and back-up strategy, design, hardware, and support for all lab data

For more information about the Ion Reporter Server System and related products, please download the Ion Reporter Server System flyer below.

MicroSEQ™ ID 16S rDNA Full Gene Library v2.0 (Applied Biosystems™)

The MicroSEQ® ID 16S rDNA Full Gene Library v2.0 is designed for installation with the MicroSEQ® ID analysis software. It contains the complete 16S sequence from bacterial organisms that can be compared to an unknown bacterial sequence using MicroSEQ® ID analysis software to identify bacteria.

MicroSEQ® ID Analysis 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 ensures you get the answers you need.
• Easy-to-use interface and optimized search algorithms enable quick results.
• Phylogenetic trees provide a deeper understanding of your unknowns.
• Security features support 21 CFR Part 11 compliance, enabling the software to integrate smoothly into your workflow.

Confidently Identify Microbes
The MicroSEQ® system comprises bacterial libraries of 500 bp sequences and of over 1,400 validated entries--including extensive coverage of gram-negative nonfermenters, Bacillus, Coryneforms, Mycobacteria, and Staphylococcus. Another library containing more than 900 entries is available for fungal identification. To ensure you can accurately identify 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.

Flexible and Easy-to-Use
To simplify microbial sequence identification, analysis, and reporting, MicroSEQ ID Analysis Software provides easy-to-use wizards and a powerful, automated toolset. The software also includes a full complement of audit-trail and security features that support 21 CFR Part 11 compliance. Further, this flexible software even allows you to create customized entries for specific sequences from new or proprietary strains.

The MicroSEQ® System: A Complete, Integrated Solution
Streamlining every step in microbial identification, Applied Biosystems MicroSEQ System combines the advantages of MicroSEQ ID Software with easy PrepMan Ultra sample preparation reagents and protocols, MicroSEQ bacterial and fungal application kits, and industry-leading thermal cyclers and sequencing systems. To ensure optimal performance and system-wide integration, we develop and test all components of the system together.

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

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 v4.0, client installation (Applied Biosystems™)

This client version of GeneMapper® Software v4 installs the client configuration (user interface) only. Users must install GeneMapper® Software 4, 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.

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.

G5v2 Module CD for 310 Genetic Analyzer (Applied Biosystems™)

This is a G5v2 Module for use in the 310 Genetic Analyzer.

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

Variant Reporter™ Software v1.1, 30 Day Demo (Applied Biosystems™)

The Variant Reporter® Software performs comparative sequencing, also known as direct sequencing, medical sequencing, PCR sequencing and resequencing with DNA sequencing files. The software is designed for reference based and non-reference based analysis such as mutation detection and analysis, SNP discovery and validation and sequence confirmation. The robust algorithms will call SNPs, mutations, insertions, deletion and heterozygous insertions⁄deletions for data generated using the Applied Biosystems® Genetic Analyzers.

There are two ways to obtain the 30-day demo software
1. Register and download the free demo Variant Reporter® Software:
http:⁄⁄marketing.appliedbiosystems.com⁄mk⁄get⁄VARIANT_REPORTER0507_LOGIN?isource=fr_E_AB_Product_Page

2. Add the 30-day demo CD (part number 4385270) to your shopping basket and it will be shipped to you for free.

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.