Alternatives to QIAGEN CLC Genomics Workbench

Labguru, a cloud-based Electronic Lab Notebook, LIMS and Informatics Platform that offers a complete solution to life science research and industry, is secure and reliable. It records and manages laboratory data, inventory, molecular biology tools, and chemistry tools. This allows labs to run more efficiently and automates lab operations. Labguru allows scientists to design experiments and workflows. They can also capture structured and unstructured information, manage projects, and share their results. You can create custom-designed experiment templates and integrate protocols, SOPs and other cutting-edge features to improve data quality, streamline workflows, and reduce costs. Labguru is available via the cloud on desktops as well as mobile devices. Labguru is part Holtzbrinck Publishing Group. It serves more than 100,000 scientists from universities, research institutes, startups, and large pharma companies around the world.

The [FP]-LIMS modules rely on a powerful SQL database solution. These modules allow for quick queries and data processing. We guarantee maximum user friendliness. Our job server is the central element of automation, which executes event- and time-controlled tasks. To monitor limit values and send an alarm message (email, message on monitor, etc.) automatically. When they are exceeded. Modern LIMS software, including modules such as inspection planning, workflow management, and analysis management, can help you design your quality management system in the most efficient way. This will make your production processes more efficient.

Geneious Prime makes bioinformatics more accessible by transforming raw information into visualizations which make sequence analysis intuitive. Simple assembly of sequences and easy editing contigs. Automatic annotation of gene prediction, motifs and translation. Genotype microsatellite trace with automated ladder fitting, peak calling, and generation of tables of alleles. A highly customizable sequence view displays beautiful visualizations of annotated assemblies and genomes. SNP variants analysis with powerful SNPs, RNA-Seq analysis and amplicon metagenomics. Create your own searchable database of primers, test PCR and sequence primers, and design and test them. CRISPR tools are powerful and make it easy to analyze your editing results, find sites, and design guide RNAs. Pre-processing NGS data with extensive tools for downstream analysis produces clean sequences. Create phylogenetic tree using peer-reviewed algorithms.

OmicsBox, a leading bioinformatics tool, offers end-toend data analysis for genomes, transcriptomes and metagenomes. It also provides genetic variation studies. The application, which is used by leading private and public research institutes worldwide, allows researchers to process large and complicated data sets and streamline their analytical process. It is designed to be efficient, user-friendly and equipped with powerful tools to extract biological insight from omics data. The software is divided into modules, each of which has a set of tools and features designed to perform specific types of analyses, such as de novo genome assemblies, genetic variations analysis, differential expression analyses, taxonomic classifications, and taxonomic classes of microbiome, including the interpretation of results and rich visualizations. The functional analysis module uses the popular Blast2GO annotating methodology, making OmicsBox a great tool for non-model organisms research.

Illumina DRAGEN Secondary Analysis is a comprehensive and accurate analysis of next-generation sequence data. Machine learning and graph reference genome drive unprecedented accuracy. Ultra-efficient workflow. Can process a whole 34x human genome in under 30 minutes using DRAGEN server version 4. Reduces FASTQ files up to 5x, resulting in an ultra-efficient workflow. Analyzes data from next-generation sequencing (NGS), including whole genomes, transcriptomes, methylomes and exomes. Available on the platform of your choice and scalable according to needs. DRAGEN analysis is the most accurate for germline and somatic mutation calling, as demonstrated by precisionFDA's industry challenges. DRAGEN analysis allows labs of any size and discipline to do more with genomic data. DRAGEN analysis is based on highly reconfigurable FPGA technology to provide hardware-accelerated implementations for genomic analysis algorithms.

Stop messing around with broken informatics tools and cloud infrastructure. Get started today on uncovering biological insights. Scientists are often limited by the fragmentation of tools across biology and bioinformatics teams. To help teams accelerate their R&D, we created a harmonized platform for bioinformatics between the cloud and the wet lab. Import raw data from your cloud service provider, your team's instruments, or your cloud. Create and deploy custom bioinformatics workflows using any language. Stop wasting time tinkering with your infrastructure. You can easily run any workflow and keep track of every analysis. Interactive visualizations of NGS data ready-to-go with point-and click plots Latch integrates with your AWS S3. You can access hundreds of terabytes in organic filesystems you are familiar with. Create bioinformatics workflows, and dynamically create no-code interfaces with Python with tunable storage and compute.

Pluto was founded in 2021 by the Wyss Institute of Harvard University. It has been a trusted partner for many life sciences organizations across the country, from biotech start-ups and public biopharma companies. Our cloud-based platform allows scientists to manage all their data, run bioinformatics analysis, and create interactive visualizations that are published-quality. The platform is being used for a variety of biological applications. These include preclinical and translational science research, cell and gene therapies and drug discovery and development.

Universal Analysis Software (UAS), a platform that analyzes and manages forensic genomic data, simplifies complex bioinformatics. The UAS is an all-inclusive solution that includes analysis modules for all ForenSeq workflows, including ForenSeq MainstAY and ForenSeq Kintelligence. It also contains ForenSeq DNA Signature prep, ForenSeq DNA Whole Genome, ForenSeq Control Region, ForenSeq mtDNA Whole Genome and ForenSeq UAS Control Region. UAS quickly generates FASTQ files and performs alignment. It also calls forensically relevant variants using NGS data. The extensive testing behind UAS's variant calls ensures that they are reliable and deliver accurate results in a user-friendly package that does not require per-seat licenses. UAS is a tool for forensic analysts. It streamlines the handling of base-bybase sequence information. It also includes a variety of features that allow you to perform everything from a quick review of everyday STR profiles to detailed analysis on the most difficult samples.

Store, archive, and manage multi-omic data sets. Illumina Connected Analytics provides a secure platform for genomic data to operationalize informatics, and drive scientific insight. CWL and Nextflow allow you to easily import, build and edit workflows. Leverage DRAGEN bioinformatics pipelines. Organize your data in a safe workspace and share it with the world in a compliant way. Our platform allows you to keep your data in the cloud. Visualize and interpret data using a flexible analysis tool, such as JupyterLab Notebooks. Data warehouses allow you to aggregate, query and analyze sample data and population data. Scale analysis operations through the creation, validation, automation, and deployment of informatics pipelines. Reduce the time needed to analyze genomic data when quick results are a key factor. Enable comprehensive profiling for the identification of novel drug targets and biomarkers of drug response. Data can be transferred seamlessly from Illumina sequencing platforms.

A robust platform for automatic variant prioritization and clinical interpretation, as well as report generation, is essential to ensure efficient reporting of NGS-based clinical trials. Strand Omics, a cloud-based platform that is HIPAA-compliant and fast, drives our clinical diagnostics practice. It has been refined over 4 years with over 10,000 clinical reports and multiple peer reviewed publications. Strand Omics is a combination of bioinformatics algorithms and curated databases, visualization interfaces, and reporting capabilities. It offers specialized workflows that can be used for rare inherited disorders and somatic tumor profiling tests. The platform has over 10,000 variants curated to oncogenicity, 100 genes that are curated for druggability across multiple types of cancer, and 500 drugs that have been curated for evidence.

GenomeStudio Software allows you to visualize and analyze data from Illumina array platforms. This powerful tool supports genotyping analysis of microarray datasets. Performance-optimized tools and a user-friendly graphical interface enable you to convert data into meaningful results quickly and easily. Analyze SNP/CNV data across 5,000,000 probes and markers. Detect outliers in sample data. Analyze differentially expressed genes across multiple genomes. Profile miRNA expression. Combine microRNA and mRNA data into one project. Single-base resolution detection of cytosine methylation. Identify methylation signatures throughout the entire genome. Illumina's goal is to use innovative technologies to analyze genetic variation and function. This will allow us to do studies that were impossible just a few short years ago. We believe it is vital to provide innovative, flexible, and scalable solutions that meet the needs of customers.

Partek bioinformatics software provides powerful visualization and statistical tools in an intuitive interface. Researchers of all levels can explore genomic data faster and more efficiently than ever before. We turn data into discovery®. Our intuitive interface makes it easy for scientists to perform sophisticated array and NGS analysis using pre-installed workflows. Public and custom statistical algorithms can be used together to quickly and accurately distill NGS data into biological insights. Genome browser, Venn diagrams and heat maps, as well as other interactive visualizations, show the biology of your next generation sequencing and array data in vivid color. Our Ph.D. scientists can be reached at any time to assist with your NGS analysis. This product is specifically designed for next-generation sequencing applications that require high-level computing. It offers flexible installation and management options.

Data management and simplified Bioinformatics are ideal for labs that are just getting started or for those who want to scale up their next-generation sequencing operations quickly. BaseSpace Sequence hub is an integral part of the BaseSpace Suite and is a direct extension to your Illumina instruments. BaseSpace Sequence hub allows you to manage your data with ease using a set of curated analysis apps. BaseSpace Sequence hub is powered by Amazon Web Services. Provides a secure environment. You can set up runs and monitor the quality of instrument runs. By converting sequence data into a standard format, and streaming it directly to the cloud, this tool promotes efficiency. Access to computing resources is available without the need for capital expenditures. Access to a variety of genomic analysis apps, whether provided by you, Illumina or third parties, increases organizational productivity.

ESP is a unified, composable, and bimodal platform with a single data fabric that reduces the total cost of operations while enabling digital transformation for life sciences + healthcare. This FDA-compliant platform includes a number of best-in-class apps, including ELN, LIMS and Sample Management. ESP's REST API library and Python SDK enable flexibility and extensibility to meet customer-specific requirements. Each release is constantly updated with new applications. ESP ships with a wide range of pre-built connectors to lab Instruments, bio-process equipment, analytics, AI/ML, 3rd party software systems (such as ERP, CRM, EMR, etc.) logistics systems, bar-code printers, etc.

Correlation Engine, an interactive omics database, places private omics data into a biological context by combining it with highly curated publicly available data. Correlation Engine, one of the largest databases in the world for life science research, provides researchers with unprecedented access and insight to a vast number of high-quality whole genome analyses. The knowledgebase allows for novel discoveries through the interrogation of billions of datapoints derived from standard analyses of whole genome studies. A suite of applications for determining biological context, a constantly growing library of curated datasets, and support of multiple species and multi-omic data sets. Use a simple graphical interface to leverage guided workflows and APIs. Accelerate the journey from omic to decision-making and gain access to more than 25,000 multi-omics studies that have been reanalyzed (from over 250.000 signatures).

Emedgene streamlines tertiary analyses for germline research and rare disease genomics. Emedgene was designed to speed up the time and certainty of user-defined variant interpretations, prioritizations, curations, and research reports. Automate your tertiary analyses with explainable AI and automation that supports genomes, exomes and virtual panels. Unify your NGS instruments and your IT systems in order to simplify and secure the entire workflow. With the latest knowledge graph options, curation abilities, and a team to support you, you can confidently keep up with evolving science, technologies, and demand. Automated workflows and explainable AI (XAI), which can be used to increase throughput without adding more staff, are a great way to do this. Implement a high-throughput WGS,WES, virtual panel or targeted panel workflow integrated into your lab's ecosystem.

The XetaBase platform is unique in that it simplifies tertiary analyses by aggregating, indexing and enriching secondary genome data. This allows for a continual reinterpretation of the data to unlock clinical and research insights. XetaBase enables the rapid management of genomic data and its cost-effective use in the laboratory and clinic. XetaBase is a genomic-scale platform. The greater the volume and the complexity, the better the insights and outcomes. XetaBase, a genomic-native platform, is built on the OpenCB open-source software platform. It meets the demands of genomic medicine for speed, scale, and reinterpretation. Zetta Genomics provides genomic data management that is fit for the precision-medicine age. XetaBase offers a novel solution for the challenges of genomic information. It replaces outdated flat file approaches and brings meaningful and actionable genome data to the lab and clinic. XetaBase allows for continual reinterpretation and scales seamlessly as databases expand to include genome sequences.

Qlucore Omics Explorer makes it so simple to use that you don't have to rely on a specialist in bioinformatics for analysis and exploration of your Omics or NGS data sets. Qlucore Omics Explorer, a next-generation D.I.Y bioinformatics software, is available for research in academia, life science, and plant-tech industries. The flexible and powerful visualization-based data analysis tool delivers instant results and allows for the exploration and visualization of large data. The software was designed to allow you to choose the best workflow for your experiments and maximize the results of your research. You will be able see your results instantly by combining instant visualization with powerful statistics, flexible selection methods, and powerful statistics. You decide the workflow and starting point for your own exploration. You have complete control over the exploration process and can tailor it to your needs.

IDBS Polar is the first BioPharma lifecycle management (BPLM) platform in the world. It eliminates repetitive manual tasks and allows you to execute your processes efficiently while curating data. This will allow you to accelerate the time to market, by tackling the most challenging challenges of process design, optimization scale-up and technology transfer. Interactive data analytics applications such as bioreactor comparision designed specifically for biopharmaceutical development scientists. IDBS Polar is an integrated platform that manages drug progress in contexts such as workflow, integration and insight. Workflows designed for the BioPharma lifecycle, with process-aware design, planning, and execution. Integrations that give meaning to your data. Rapid integration into your development environment, enabling automation, and curating a data backbone based on processes.

Legacy R&D software can be a drain on scientific potential. It slows down R&D progress and scatters data between silos. Benchling is the industry's most trusted life sciences R&D cloud. All the tools you need to accelerate, measure, and forecast R&D, from discovery through bioprocessing, all in one place. A suite of seven applications that are natively unified and can be used to accelerate R&D at all levels. Open integration, codeless configuration, and dashboards that are tailored to your needs. For continued success, deep life science R&D and consulting expertise are essential. Benchling is a unified R&D platform that allows you to spend less time searching for data and more time working together in order to advance your research. Scientists, managers, executives, and researchers can optimize R&D output by having complete visibility into the experimental context, program performance, resource utilization, and program performance.

g.nome is a cloud-native, workflow-optimized platform that provides streamlined, scalable and interoperable workflows to perform next-generation sequencing analyses. g.nome offers a low-code/no code pipeline build. Using pre-built toolkits and workflows from a curated collection, g.nome gives researchers the power to import custom code and handle large datasets reliably. With g.nome you can remove long-standing barriers related to workflow language, visibility of process flow, and quality control. All that's left is streamlined, interoperable, and scalable genomic workflows. This allows research teams to focus on what they do best, which is the science.

Eidogen-Sertanty’s Target Informatics platform (TIP), is the first global structural informatics system. It enables researchers to examine the druggable genome from an structural perspective. TIP increases the rapidly expanding body experimental protein structure information and transforms structure based drug discovery from an inefficient, data-scarce discipline to a high-throughput science with rich data. TIP is a tool that bridges the knowledge gap between bioinformatics (bioinformatics) and cheminformatics. It provides drug discovery researchers with a knowledge bank of information that is both unique and highly complementary to existing bio- and cheminformatics platform information. TIP's seamless integration between structural data management technology and unique target-to-lead analysis capabilities enhances every stage of the discovery pipeline.

Founded in order to improve lives through high-value care, the hc1 platform has become a leader in bioinformatics for precision prescribing and testing. The cloud-based hc1 high-value care platform® organizes large amounts of live data, including genomics and medications, to provide solutions that ensure the right patient receives the right test and prescription. The hc1 Platform is a platform that powers solutions that optimize diagnostic testing, prescribing, and patient care for millions of patients across the country. Visit www.hc1.com to learn more about the proven approach of hc1 to personalizing care and eliminating waste for thousands upon thousands of health systems, diagnostic labs, and health plans.

Ruffus is a Python computation pipeline library. It is open-sourced and powerful, user-friendly, and widely used for science and bioinformatics. Ruffus was designed to automate scientific and other analyses with minimal fuss and effort. It is suitable for even the most basic tasks. Even complex pipelines can be handled. This will prevent make or scons from becoming cross-eyed and recursive. No "clever magic", no pre-processing. The lightweight syntax, which does one small thing well, is unambitious. Ruffus is licensed under the permissive MIT-free software license. This license allows for free use and inclusion in proprietary software. It is a good idea to run your pipeline in a temporary directory that is not connected to your original data. Ruffus is a lightweight Python module that can be used to build computational pipelines. Ruffus requires Python 2.6 and higher, or Python 3.0 and higher.

Dotmatics is the global leader in R&D scientific software that connects science, data, and decision-making. More than 2 million scientists and 10,000 customers trust Dotmatics to accelerate research and help make the world a healthier, cleaner, and safer place to live.

HyperProtein, Hypercube, Inc.'s latest product, focuses on the computational science of protein sequences. The product allows you to analyze one-dimensional sequences of protein as well as subsequent three-dimensional structures. The product's most important feature is the relationship between structure and sequence. HyperProtein is not like other software programs that can perform specific functions, such as sequence alignment or protein sequence sequence, but it does combine a variety of Bioinformatics tools and Molecular Modeling tools that are related to the science that begins with a protein sequence.

Ensure seamless data integration and top-notch informatics management. iLES is a single-stop communication, documentation storage, and workflow hub for your entire organization. It works in real time. iLES supports LIMS (Lab Information System), ELN(Electronic Lab Notebook), SDMS [Scientific Data Management System] and DMS (Data Management System). Regardless of which digital stage your lab is at or what system it is replacing, iLES uses vendor neutral technologies to integrate your data. To manage all communications and lab needs, you will only need one system, iLES. Automated upgrades and rapid feature release. Access information securely from anywhere on the planet using any device that has an Internet connection. Technology that is vendor-neutral helps transform laboratories into paperless, tightly integrated environments.

Polly allows you to harness the power of biomedical information. The Polly Platform allows you to scale batch jobs, workflows and visualization applications. Polly supports resource pooling, optimizes resource allocation based upon your usage requirements, and makes use of spot instances when possible. This results in optimization, efficiency, quicker response time, and lower costs for resources. Access a dashboard that allows you to monitor and track resource usage and costs in real-time. This will allow you to reduce overheads when resource management is done by your IT team. Polly's infrastructure is built around version control. Polly uses a combination dockers and interactive notebooks to ensure version control for your analyses and workflows. We have created a mechanism that allows data, code, and the environment to co-exist. This, along with cloud data storage and the ability for users to share projects, ensures reproducibility in every analysis.

Microsoft's experience and scale in managing exabyte-scale workloads can be used to reduce the need for you to manage your own data center. Microsoft Genomics on Azure gives you the performance and scalability that comes with a supercomputing facility of the highest caliber, all on demand. Take advantage of an MPI backend network that has a latency of under three microseconds, and a non-blocking throughput of 32 gigabits per seconds (Gbps). This backend network features remote direct memory access, which allows parallel applications to scale up to thousands of cores. Azure offers high memory and HPC class CPUs to help get results quickly. Scale up or down according to your needs and only pay for what you actually use. Azure's worldwide network of data centers can help you meet your compliance needs and address data sovereignty issues. Easy integration into your existing pipeline code with a REST API and simple Python client.

Swiss-PdbViewer, also known as DeepView, is an application that allows you to analyze multiple proteins simultaneously. To compare active sites and other parts, the proteins can be superimposed. The intuitive interface and graphic make it easy to find information about amino acid mutations, Hbonds, angles and distances between atoms. Nicolas Guex has been developing Swiss-PdbViewer (aka DeepView), since 1994. Swiss-PdbViewer was originally tightly connected to SWISS-MODEL (an automated homology modeling server) that was developed at the Structural Bioinformatics Group of the Biozentrum in Basel. The SWISS-MODEL interface has evolved to the point that advanced modeling can now be done directly. It is no longer possible to maintain a direct interface with SwissPdbViewer.

We are now in the next era for human identification. We provide more than just the traditional DNA profile. We offer better answers to solve the most difficult mysteries. Our comprehensive portfolio of next generation sequencing (NGS), solutions will help you take your forensic investigations to the next level. We offer a variety of capabilities that will allow you to make the identifications that you need. We offer modern alternatives to traditional methods and can help you improve your operations today as well as prepare you for the analyses of tomorrow. Our NGS workflow is flexible and adaptable to multiple applications. It can also be scalable and integrated seamlessly into your existing laboratory environment. Using mtDNA analysis, even the most difficult, compromised or degraded DNA samples can be saved.

The most widely used LIMS (Laboratory Information Management System) is the best way to increase productivity, ensure compliance, streamline operations, and improve organizational efficiency. Thermo Scientific's SampleManager LIMS™, which combines laboratory management, data management (SDMS), and process execution/procedural ELN(LES) capabilities, is the world's most widely used LIMS. SampleManager LIMS is used by laboratories in all industries including pharmaceutical, food, beverage, oil and natural gas, manufacturing, contract testing, and water and environmental.

You can seamlessly combine and collect a variety data in a single software platform. Automatic synchronization and electromyography are combined to create a smarter workflow. Even with complex biomechanics record systems, collection, review, analysis, reporting, and reporting are now simplified. MyoRESEARCH®, module configurations make it easy to select the devices that will be used for your session. Your data will automatically be time synchronized.

Scilligence SDMS is a centralized storage solution that integrates with a variety of instruments and devices. This allows scientists to quickly and securely access the data they require. SDMS automation allows the retrieval of scientific data from instruments, equipment or devices, and the extraction and storage of metadata in a relational data base. This streamlines data management and reduces costs. We offer strict version control, detailed audit histories, and a history of document changes that are aligned with common regulatory compliance standards. SDMS is compatible with lab devices and instruments for automated data retrieval. It also integrates seamlessly with Scilligence applications. We also allow the integration of other storage and database solutions. Protect your intellectual property with site, account and project-level access control.

The Suite is secure and scalable. It features an intuitive interface that allows scientists to configure workflows for any technique, modality, or data type. Signals VitroVivo 3.0, formerly Signal's Screening, transforms raw data into actionable findings. Signals Inventa 3.0, formerly Signals Lead Discovery is the next-generation analytics software that allows researchers to seamlessly publish results across disparate data sources. A cloud-based electronic notebook that is easy to use allows for experimental data capture, materials management, collaboration workflows, and more. Flexible visual and automated instrument data processing to improve data quality and reproducibility. Rich interactive analytics and unified data management for scientific research results. Integration with partner systems and processes as well as internal systems is possible.

Flywheel provides comprehensive data management solutions to researchers looking to improve productivity and collaboration in imaging research and clinical trials, multi-center studies, and machine learning. Flywheel provides end-to-end solutions that streamline data ingestion and curate it to common standards. We also automate processing and machine-learning pipelines. Our platform allows for secure collaboration in the life sciences, clinical, academic, as well as AI, industries. Cross-platform data and algorithm integration, secure and compliant data discovery among a global network, and cloud-scalable and on-premise computational workflows to support research and clinical applications. Flywheel is a data curation platform that supports multi-modality research. It can manage a wide range of data types, including digital pathology, imaging files, clinical EMR data and omics, as well as instruments.

Govalidation, a web-based app that allows you to validate your life cycle digitally, is called Govalidation. A configurable workflow allows for the automatic review and approval of the cycle. The system was designed in compliance to 21 CFR Part 11 and regulatory requirements. Industry experts provided inputs and the best standards were followed. Facilitates best practice system for method validation. Each URS is assessed using a risk-based approach. This allows for the development of a medication plan and testing case to mitigate the risk. Digital transformation eliminates 100% of paper-records Integrated deviation management enables paperless test execution. Manual errors can be avoided or minimized. Clarity in the execution of validation projects with detailed view of project status as of date. Audit ready system with real-time data for review.

Arxspan's Electronic Lab Notebook, a cloud-based platform for scientific data management, combines biology and chemistry data in one system. It is designed to facilitate collaboration between internal teams and external partners. Single cloud ELN supports chemistry and biology experiments. Advanced, chemical, and keyword searching. Attachment and inline editing for all Microsoft Office, image and instrument files. The private, secure Arxspan Cloud environment allows for deployment without the need for hardware maintenance, acquisition, or IT overhead. Integration with legacy electronic laboratory notebooks systems is possible out of the box. View and/or create sharing capabilities at the notebook and project levels. Configurable permission hierarchy and user roles. Test signing and witnessing workflows. SAFE BioPharma compatibility with multi-factor capabilities. Support for system validation and system updates

Avogadro, an advanced molecule editor/visualizer, is designed for cross-platform usage in computational chemistry and molecular modeling. It provides high-quality rendering and a powerful plugin structure. Avogadro, a free and open-source molecular editor/visualization tool, is available for Mac, Windows, and Linux. It can be used in computational chemistry and molecular modeling as well as materials science and other related areas. It provides flexible, high-quality rendering and a powerful plugin structure.

We build products with our in-house chemists, biologists and clients to deliver outstanding performance and scientific understanding. Chemaxon offers a wide range of products, including out-of-the box solutions for scientists and IT professionals. It also includes components that add extra functionality as well as integrations with 3rd-party software, such Microsoft Excel or KNIME. Chemaxon, a leading software provider, is trusted by more than one million users. Its industry-leading tools for scientific discovery include calculation, search, and drawing tools. Our applications are used widely in education and research in the life sciences. Our clients come from a wide range of industries. The majority of major pharmaceutical companies are among them. Our offices are located at Budapest, Basel and Boston, with distributors all over the world.

ScienceDesk data automation simplifies the use of artificial intelligence (AI) in materials sciences. Your team can easily add and apply the latest AI algorithms every day with this practical tool. You can customize properties, universal identifiers and QR-codes. There is also a textual-numeric search engine that links experimental and sample data. ScienceDesk allows scientists and engineers to collaborate and gain insights into their experimental data through an innovative platform. This asset's potential is not fully tapped due to the complexity of data formats and dependence on experts to extract specific information. ScienceDesk's research data management system, ScienceDesk, solves this problem by combining data analysis and documentation in a well-designed data structure. Our algorithms give scientists and researchers the ability to have complete control over their data. They can share data and analysis knowledge.

LabSpeed™, Results Analysis software allows you to share, chart, report, export, monitor, validate, share, and analyze results from all types of instruments in a laboratory. These instruments can be hand-held devices, multi-element analysis spectrumrometers, bio-tech instruments, or handheld devices. You can access your instrument data instantly with minimal or no setup. LabSpeed automatically handles data connections and formats. It is easy to quickly create the solutions that a laboratory needs on a daily basis in a drag-and-drop interface. LabSpeed can simultaneously work with data from any type of analytical instrument, regardless of its complexity. LabSpeed can be used at the instrument to review, export and print data, or in the office for advanced publishing, research, data analysis, and data analysis. LabSpeed offers advanced capabilities and features that are not available in other software packages like Crystal Reports®, SigmaPlot® or InfinityQS®.

Logilab SDMS is an established and reliable Scientific Data Management System that can capture data from any type, make, or manufacturer of analytical instrument, making it a versatile tool for scientific research and experimentation. This system allows for the capture and archiving of both instrument data and metadata to a secure and dedicated server, which serves as a single point of truth for all scientific data. Logilab SDMS has been primarily designed to capture, catalog, and archive instrument raw data and files, along with their associated metadata. The tagging system enables data to be indexed into catalogues and archived for long-term purposes, ensuring that scientific data is readily available whenever it is needed. Furthermore, with Logilab SDMS, laboratories can confidently face audits knowing that their scientific data is organized, archived, and readily available for review.

Scitara DLX™ provides a fast connectivity infrastructure for any instrument used in life science laboratories. It is fully compliant and auditable, and can be accessed from any cloud-based platform. Scitara™, a universal digital data network, connects all instruments, resources, apps, and software within the laboratory. The cloud-based platform, which is fully auditable, connects all data sources in the lab, allowing data to flow freely across multiple endpoints. Scientists can now spend their time on scientific research and not waste it trying to solve data problems. DLX corrects and curates flight data to support the creation of precise, structured data models that feed AI/ML systems. This supports a successful digital transformation strategy for the pharma and biopharma sectors. The ability to access scientific data allows for faster decision-making and drug discovery, which helps bring drugs to market quicker.

StackWave's Laboratory Information Management System, Electronic Laboratory Notebook (ELN), or Scientific Data Management System, (SDMS), are innovative, flexible and innovative software solutions that will improve the efficiency of your laboratory. Let StackWave automate your tedious scientific processes so that your team can concentrate on what is important. StackWave's lab software is perfect for labs of any size and in any industry. Our solutions can support a wide range of processes. We have worked with teams from small biotechs to large pharmaceutical companies. The StackWave LiMS is the most advanced laboratory information management system. It combines the best of web, database and software technologies. The StackWave LiMS is built on StackWave’s proven software infrastructure and provides the flexibility, reliability, performance, and performance you need to meet your most challenging information management challenges.

NuVerve is a collaborative SaaS that offers Scientific Data Intelligence for scientists. It provides a set easy-to-use features to structure data, create custom analyses, and automatically generate reports. NuVerve, priced at $75/month, is available to all scientists.

Cytobank, a cloud-based platform that allows for analysis, storage, sharing, and sharing of mass cytometry data, is available. Cytobank can be accessed via the internet using a web browser and an existing account. Cytobank does not require any additional software or hardware to be installed, updated, or maintained. Both license types have the same functionality. This license is ideal for large research groups, pharma, biotech R&D teams, clinical research organizations, and other clinical research organizations. Private Cloud, Access is controlled by an administrator role. Larger compute caps for functionality such as viSNE

LabSolutions LC/GC is a software platform that improves software operation. It allows simultaneous control and analysis up to four LC/GC system and data, making it more user-friendly. LabSolutions DB, a SQL-based platform, integrates a data management function and LabSolutions LC/GC. It is also compliant with ER/ES Regulations. Other vendor's HPLCs or GCs can also all be controlled. LabSolutions CS is able to read data from any computer connected to a network, as all data for analytical purposes is stored in a database on a server computer. A client PC can also be used to perform analysis directions, instrument monitoring, and control. LabSolutions CS can also be used to manage servers and is compatible with Citrix XenApp. LabSolutions C/S allows for the management of data from spectroscopy instruments and other vendors' HPLCs and GCs in addition to Shimadzu chromatography.

LabVantage is a platform that combines laboratory information management system, electronic lab notebook (ELN), lab execution (LES), and scientific database management system (SDMS). It allows labs to be productive and efficient. LabVantage can be deployed intelligently via a zero-footprint web browser-based interface. It is available for all sizes of enterprises as pre-packaged solutions to specific industries and via on-premise or cloud-hosted SaaS implementations. Our solutions are designed to help lab managers, scientists, technicians, and researchers better manage everything, from instruments and materials to reports and regulatory compliance to data integrity.

LabKey platform unlocks the power of your data to accelerate life-changing discovery. We believe your time should be spent on your research and not battling information bottlenecks. Our team uses their years of experience to provide reliable and intuitive solutions for managing your research. Your data is the key to life-changing scientific insights. LabKey's biology-aware data management platform allows teams to centralize and organize complex data in order to support discovery. It is crucial that you are able to understand, treat, cure, and eventually eliminate disease. We are committed to helping you achieve your mission. This is why we offer exceptional software solutions and support.