Alternatives to Loupe Browser
Compare Loupe Browser alternatives for your business or organization using the curated list below. SourceForge ranks the best alternatives to Loupe Browser in 2026. Compare features, ratings, user reviews, pricing, and more from Loupe Browser competitors and alternatives in order to make an informed decision for your business.
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TheLoupe
TheLoupe
TheLoupe® jewelry appraisal software is the most powerful tool for your appraisal business. TheLoupe® jewelry appraisal software is the most powerful tool for your appraisal business. Our online appraisal software is designed for both the beginner and experienced appraiser to learn easily. TheLoupe® allows you to effortlessly move through a complete appraisal with accuracy and speed, even when updating and archiving files. With our online appraisal software, you can create consistent and professional appraisals. TheLoupe® allows you to add a custom logo, has easy-to-use templates, calculates gem-weights in real-time, and much more. TheLoupe® features digital imaging, online plotting, real-time updates, and built-in customer follow-ups.Starting Price: $24.99/month/user -
2
Parse Biosciences Evercode
Parse Biosciences
Combinatorial barcoding technology strips away the limitations and frustrations of yesterday’s single-cell approach. It ditches the specialized instrument, freeing you to pursue unprecedented discoveries. Unleash the potential of a single cell. Profile from 1000 to 1 million cells or nuclei in a single experiment, offering unparalleled scientific progress. Evercode combinatorial barcoding technology blows droplet-based approaches out of the water. Expand the size of your experiments without the limitations of yesterday’s restraints. Get better data quality. All without the need for finicky hardware that’s already out of date. Perform single-cell experiments with nothing more than a pipette and common laboratory equipment. Split-pool combinatorial barcoding enables scalable single cells without any custom instrument. Scalable single-cell sequencing without the instrument. Each kit provides end-to-end solution reagents and intuitive analysis software. -
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CZ CELLxGENE Discover
CZ CELLxGENE
Select two custom cell groups based on metadata to find their top differentially expressed genes. Leverage millions of cells from the integrated CZ CELLxGENE corpus for powerful analysis. Execute interactive analyses on a dataset to explore how patterns of gene expression are determined by spatial, environmental, and genetic factors using an interactive speed no-code UI. Understand published datasets or use them as a launchpad to identify new cell sub-types and states. Census provides access to any custom slice of standardized cell data available on CZ CELLxGENE Discover in R and Python. Explore an interactive encyclopedia of 700+ cell types that provides detailed definitions, marker genes, lineage, and relevant datasets in one place. Browse and download hundreds of standardized data collections and 1,000+ datasets characterizing the functionality of healthy mouse and human tissues. -
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BioTuring Browser
BioTuring Browser
Explore hundreds of curated single-cell transcriptome datasets, along with your own data, through interactive visualizations and analytics. The software also supports multimodal omics, CITE-seq, TCR-seq, and spatial transcriptomic. Interactively explore the world's largest single-cell expression database. Access and query insights from a single-cell database of millions of cells, fully annotated with cell type labels and experimental metadata. Not just creating a gateway to published works, BioTuring Browser is an end-to-end solution for your own single-cell data. Import your fastq files, count matrices, Seurat, or Scanpy objects, and reveal the biological stories inside them. Get a rich package of visualizations and analyses in an intuitive interface, making insight mining from any curated or in-house single-cell dataset become such a breeze. Import single-cell CRISPR screening or Perturb-seq data, and query guide RNA sequences.Starting Price: Free -
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Loupe
Loupe
Know when issues happen in your application with Loupe. A logging and application monitoring solution for .NET and Java, Loupe helps software teams monitor, find, and fix errors in their applications the first time. It also gives users the visibility into events and key metrics for all applications, and offers the ability to dig deeper into specific events, sessions, users, and machines. Loupe can be deployed on-premise or as a cloud hosted solution.Starting Price: $25.00/month -
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Cellenics
Biomage
Turn your single-cell RNA sequencing data into meaningful insight with Cellenics software. Biomage hosts a community instance of Cellenics, an open source analytics tool for single-cell RNA sequencing data that has been developed at Harvard Medical School. It enables biologists to explore single-cell datasets without writing code and helps scientists and bioinformaticians to work together more effectively. It takes you from count matrices to publication-ready figures in just a few hours and can be integrated seamlessly with your workflow. It’s fast, interactive, and user-friendly. And it’s cloud-based, secure, and scaleable. The Biomage-hosted community instance of Cellenics is free for academic researchers with small/medium-sized datasets (up to 500,000 cells). It’s used by 3000+ academic researchers studying cancer, cardiovascular health, and developmental biology.Starting Price: Free -
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GeoMx Digital Spatial Profiler (DSP)
nanoString
Quickly resolve tissue heterogeneity and the complexity of microenvironments with the GeoMx Digital Spatial Profiler (DSP), the most flexible and robust spatial multi-omic platform for analysis of FFPE and fresh frozen tissue sections. GeoMx is the only spatial biology platform that non-destructively profiles the expression of RNA and protein from distinct tissue compartments and cell populations with an automated and scalable workflow that integrates with standard histology staining. Spatially profile the whole transcriptome and 570+ protein targets separately or simultaneously from your choice of sample inputs: whole tissue sections, tissue microarrays (TMAs), or organoids. Make GeoMx DSP your spatial biology platform of choice for biomarker discovery and hypothesis testing. Decide where to draw the line and let the tissue be your guide with biology-driven profiling that empowers you to choose the tissue microenvironments and cell types that matter most to you. -
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GenomeStudio
Illumina
Visualize and analyze data generated on Illumina array platforms with GenomeStudio Software. This powerful solution supports the genotyping analysis of microarray data. Performance-optimized tools and a user-friendly graphical interface enable you to convert data into meaningful results quickly and easily. Analyze SNP and CNV data across 5 million markers and probes. Detect sample outliers. Analyze differentially expressed genes across different genomes. Profile miRNA expression. Combine mRNA and microRNA data in a single project. Detect cytosine methylation at single-base resolution. Identify methylation signatures across the entire genome. At Illumina, our goal is to apply innovative technologies to the analysis of genetic variation and function, making studies possible that were not even imaginable just a few years ago. It is mission critical for us to deliver innovative, flexible, and scalable solutions to meet the needs of our customers. -
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GenomeBrowse
Golden Helix
This free tool delivers stunning visualizations of your genomic data that give you the power to see what is occurring at each base pair in your samples. GenomeBrowse runs as a native desktop application on your computer. No longer do you have to sacrifice speed and interface quality to obtain a consistent cross-platform experience. It was developed with performance in mind to deliver a faster and more fluid browsing experience than any other genome browser available. GenomeBrowse is also integrated into the powerful Golden Helix VarSeq variant annotation and interpretation platform. If you love the visualization experience of GenomeBrowse, check out VarSeq for filtering, annotating, and analyzing your data before utilizing the same visualization interface. GB can display all your alignment data. Looking at all your samples in one view can help you spot contextually relevant findings.Starting Price: Free -
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Partek Flow
Partek
Partek bioinformatics software delivers powerful statistical and visualization tools in an easy-to-use interface. Researchers of all skill levels are empowered to explore genomic data quicker and easier than ever before. We turn data into discovery®. Pre-installed workflows and pipelines in our intuitive point-and-click interface make sophisticated NGS and array analysis attainable for any scientist. Custom and public statistical algorithms work in concert to easily and precisely distill NGS data into biological insights. Genome browser, Venn diagrams, heat maps, and other interactive visualizations reveal the biology of your next-generation sequencing and array data in brilliant color. Our Ph.D. scientists are always just a phone call away and ready to help with your NGS analysis any time you have questions. Designed specifically for the compute-intensive needs of next-generation sequencing applications with flexible installation and user management options. -
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Evo 2
Arc Institute
Evo 2 is a genomic foundation model capable of generalist prediction and design tasks across DNA, RNA, and proteins. It utilizes a frontier deep learning architecture to model biological sequences at single-nucleotide resolution, achieving near-linear scaling of compute and memory relative to context length. Trained with 40 billion parameters and a 1 megabase context length, Evo 2 processes over 9 trillion nucleotides from diverse eukaryotic and prokaryotic genomes. This extensive training enables Evo 2 to perform zero-shot function prediction across multiple biological modalities, including DNA, RNA, and proteins, and to generate novel sequences with plausible genomic architecture. The model's capabilities have been demonstrated in tasks such as designing functional CRISPR systems and predicting disease-causing mutations in human genes. Evo 2 is publicly accessible via Arc's GitHub repository and is integrated into the NVIDIA BioNeMo framework. -
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XetaBase
Zetta Genomics
The unique XetaBase platform simplifies tertiary analysis, aggregating, indexing, and enriching secondary genomic data, enabling continual re-interpretation to unlock research and clinical insight. XetaBase accelerates data management and the cost-effective application of genomic data in the lab and clinic. XetaBase encompasses genomic scale, the greater the volume and complexity, the greater the insight and outcomes. XetaBase is a genomic-native technology, built on the open-source, OpenCB software platform to meet the scale, speed, and re-interpretation demands of genomic medicine. Zetta Genomics delivers genomic data management fit for the precision medicine age. XetaBase is a completely novel solution to the challenges of genomic data. It sweeps away obsolete flat file approaches to bring meaningful and actionable genomic data into the lab and the clinic. XetaBase empowers continual re-interpretation while scaling seamlessly as databases grow to encompass genome sequences. -
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OmicsBox
BioBam Bioinformatics S.L.
OmicsBox is a leading bioinformatics solution that offers end-to-end data analysis of genomes, transcriptomes, metagenomes, and genetic variation studies. The application is used by top private and public research institutions worldwide and allows researchers to easily process large and complex data sets, and streamline their analysis process. It is designed to be user-friendly, efficient, and with a powerful set of tools to extract biological insights from omics data. The software is structured in different modules, each with a specific set of tools and functions designed to perform different types of analysis, such as de-novo genome assemblies, genetic variation analysis, differential expression analysis, and taxonomic classifications of microbiome data, including the functional interpretation and rich visualizations of results. The functional analysis module includes the popular Blast2GO annotation methodology and makes OmicsBox particularly suited for non-model organism researchStarting Price: €100/month/seat -
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Illumina DRAGEN Secondary Analysis
Illumina
The Illumina DRAGEN Secondary Analysis provides accurate, comprehensive, and efficient analysis of next-generation sequencing data. Graph reference genome and machine learning driving unprecedented accuracy. Provides ultra-efficient workflow; can fully process a 34x whole human genome in ~30 minutes with DRAGEN server v4. Furthers ultra-efficient workflow by reducing FASTQ file sizes up to 5×. Analyzes next-generation sequencing (NGS) data from whole genomes, exomes, methylomes, and transcriptomes. Available on platform of choice and scalable based on needs. DRAGEN analysis leads in accuracy for germline and somatic variant calling demonstrated in industry challenges from precisionFDA. DRAGEN analysis enables labs of all sizes and disciplines to do more with their genomic data. DRAGEN analysis uses highly reconfigurable field-programmable gate array technology (FPGA) to provide hardware-accelerated implementations of genomic analysis algorithms. -
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Evo Designer
Arc Institute
Evo Designer is an advanced tool developed by the Arc Institute, leveraging the capabilities of the Evo 2 genomic foundation model to facilitate DNA sequence generation and analysis. This platform enables users to input nucleotide sequences or specify organisms, prompting the model to generate corresponding DNA sequences. It provides comprehensive annotations of coding regions and, for prokaryotic sequences, offers 3D protein visualizations utilizing ESMFold. Additionally, Evo Designer evaluates sequences by scoring their perplexity and per-nucleotide entropy, assisting researchers in assessing sequence complexity and variability. The underlying Evo 2 model is trained on over 9 trillion nucleotides from a diverse array of prokaryotic and eukaryotic genomes, employing a deep learning architecture that models biological sequences at single-nucleotide resolution with a context window extending up to 1 million tokens. -
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Correlation Engine
Illumina
Correlation Engine is an interactive omics knowledgebase that puts private omics data in a biological context with highly curated public data. One of the largest biological databases in the world, Correlation Engine provides life science researchers with unprecedented access to vast numbers of high-quality whole-genome analyses and insightful scientific tools. The knowledgebase enables novel discoveries by interrogating billions of data points derived from standardized analyses of whole genome studies. A suite of applications to determine biological context, a continually growing library of curated data sets, and support for multiple species and multi-omic datasets. Utilize a simple graphical user interface to leverage guided workflows, push-button applications, and APIs. Accelerate your journey from omic data to decision and get access to over 25,000 multi-omics studies (from over 250,000 signatures) that have been reanalyzed. -
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QIAGEN CLC Genomics Workbench
QIAGEN Digital Insights
QIAGEN CLC Genomics Workbench is a powerful solution that works for everyone, no matter the workflow. Cutting-edge technology and unique features and algorithms widely used by scientific leaders in industry and academia make it easy to overcome challenges associated with data analysis. User-friendly bioinformatics software solutions allow for comprehensive analysis of your NGS data, including de novo assembly of whole genomes and transcriptomes, resequencing analysis (WGS, WES and targeted panel support), variant calling, RNA-seq, ChIP-seq and DNA methylation (bisulfite sequencing analysis). Analyze your RNA-seq and small RNA (miRNA, lncRNA) data with easy-to-use transcriptomics workflows for differential expression analysis at gene and transcript levels. QIAGEN CLC Genomics Workbench is developed to support a wide range of NGS bioinformatics applications. -
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VarSeq
Golden Helix
Simple, fast, and repeatable variant analysis software for gene panels, exomes, and whole genomes. VarSeq is an intuitive, integrated software solution for tertiary analysis. With VarSeq you can automate your workflows and analyze variants for gene panels, exomes, and whole genomes. Understanding genomic data has never been easier thanks to our software. VarSeq software provides a powerful filtering and annotation engine to sift through large variant data sets. Using a chain of filters, you can quickly narrow your list of variants down to those that are most likely to be of interest. After determining the parameters that work well for your analysis, you can save the state of your filters so that you can easily apply the same analysis to another dataset. The same automated workflow can be used for each batch of samples, making VarSeq an ideal solution for high-throughput environments. Real-time filtering gives you the power to quickly prototype and tune analysis workflows. -
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Genome Analysis Toolkit (GATK)
Broad Institute
Developed in the Data Sciences Platform at the Broad Institute, the toolkit offers a wide variety of tools with a primary focus on variant discovery and genotyping. Its powerful processing engine and high-performance computing features make it capable of taking on projects of any size. The GATK is the industry standard for identifying SNPs and indels in germline DNA and RNAseq data. Its scope is now expanding to include somatic short variant calling and to tackle copy number (CNV) and structural variation (SV). In addition to the variant callers themselves, the GATK also includes many utilities to perform related tasks such as processing and quality control of high-throughput sequencing data and bundles the popular Picard toolkit. These tools were primarily designed to process exomes and whole genomes generated with Illumina sequencing technology, but they can be adapted to handle a variety of other technologies and experimental designs.Starting Price: Free -
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Alissa Interpret
Agilent Technologies
Alissa Interpret is your universal genomic data interpretation software for clinical decision support. Increase your productivity, shorten the turnaround time, and maintain regulatory compliance with Alissa Interpret’s agnostic CGH and NGS tertiary analysis platform for variant interpretation and reporting. Achieve complete operational efficiency when pairing Alissa Interpret with Agilent’s fully optimized SureSelect NGS reagents, intuitive secondary NGS analysis Alissa Reporter, Magnis walkaway automation, and TapeStation QC for a streamlined NGS data analysis workflow. External and internal curated variant knowledgebases at your fingertips. Automated variant interpretation solution accelerates CGH and NGS tertiary analysis. One platform for SNVs, InDels, CNVs, LOH, and fusions. Integrate with your LIMS and eliminate genomic data analysis bottlenecks. Connect with peers, share knowledge, and improve diagnostic yield. -
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Congenica
Congenica
We drive precision medicine and help reduce the burden on healthcare systems by delivering automated analysis, diagnosis, and treatment solutions to healthcare providers and patients worldwide. Congenica was founded on pioneering work at the Wellcome Sanger Institute and the UK NHS. Our products combine state-of-the-art technology, market-leading automation, and AI to enable our uniquely differentiated platform to be employed in all areas of human disease where genomic information is key to unlocking actionable insights. We are a digital health company providing software and solutions for the analysis and interpretation of genomic data at scale. Full automation with powerful APIs and ML to reduce the burden on specialist staff, maximize case throughput, accelerate decision-making, and streamline reporting. Certified, accurate, and secure analysis platform to support clinical decisions with the highest degree of confidence in the clinical outcome. -
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Universal Analysis Software (UAS) provides a platform for analyzing and managing forensic genomic data, simplifying complex bioinformatics. The UAS is an all-inclusive solution, containing analysis modules supporting all current ForenSeq workflows including ForenSeq MainstAY, ForenSeq Kintelligence, ForenSeq DNA Signature Prep, ForenSeq mtDNA Whole Genome, and ForenSeq mtDNA Control Region. UAS rapidly generates FASTQ files, performs alignment, and calls forensically relevant variants from NGS data. Extensive testing backs highly reliable variant calls to deliver accurate results in a user-friendly package with no per-seat licenses. Designed specifically for forensic analysts, UAS streamlines handling of base-by-base sequence information and contains a range of features to enable everything from efficient review of everyday STR profiles to detailed analysis of the most challenging samples.
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Emedgene
Illumina
Emedgene streamlines your tertiary analysis workflows for rare disease genomics and other germline research applications. Emedgene is designed to accelerate the time and certainty in user-defined variant interpretation, prioritization, curation, and research report generation. Enable greater efficiency from your tertiary analysis workflows with explainable AI (XAI) and automation supporting genomes, exomes, virtual panels, and targeted panels. Unify your laboratory and NGS instrumentation with your IT systems to simplify and secure your complete workflow. Confidently keep pace with evolving science, technology, and demand with up-to-date knowledge graph options, curation capabilities, and a team of experts to support your journey. Increase throughput without increasing headcount using explainable AI (XAI) and automated workflows. Implement a high throughput WGS, WES, virtual panel, or targeted panel workflow that is integrated into your lab's digital ecosystem. -
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Illumina Connected Analytics
Illumina
Store, archive, manage, and collaborate on multi-omic datasets. Illumina Connected Analytics is a secure genomic data platform to operationalize informatics and drive scientific insights. Easily import, build, and edit workflows with tools like CWL and Nextflow. Leverage DRAGEN bioinformatics pipelines. Organize data in a secure workspace and share it globally in a compliant manner. Keep your data in your cloud environment while using our platform. Visualize and interpret your data with a flexible analysis environment, including JupyterLab Notebooks. Aggregate, query, and analyze sample and population data in a scalable data warehouse. Scale analysis operations by building, validating, automating, and deploying informatics pipelines. Reduce the time required to analyze genomic data, when swift results can be a critical factor. Enable comprehensive profiling to identify novel drug targets and drug response biomarkers. Flow data seamlessly from Illumina sequencing systems. -
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Galaxy
Galaxy
Galaxy is an open source, web-based platform for data-intensive biomedical research. If you are new to Galaxy start here or consult our help resources. You can install your own Galaxy by following the tutorial and choosing from thousands of tools from the tool shed. This instance of Galaxy is utilizing infrastructure generously provided by the Texas Advanced Computing Center. Additional resources are provided primarily on the Jetstream2 cloud via ACCESS, and with support from the National Science Foundation. Quantify, visualize, and summarize mismatches in deep sequencing data. Build maximum-likelihood phylogenetic trees. Phylogenomic/evolutionary tree construction from multiple sequences. Merge matching reads into clusters with TN-93. Remove sequences from a reference that are within a given distance of a cluster. Perform maximum-likelihood estimation of gene essentiality scores.Starting Price: Free -
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Gzip
GNU Operating System
GNU Gzip is a popular data compression program originally written by Jean-loup Gailly for the GNU project. Mark Adler wrote the decompression part. We developed this program as a replacement for compress because of the Unisys and IBM patents covering the LZW algorithm used by compress. These patents made it impossible for us to use compress, and we needed a replacement. The superior compression ratio of gzip is just a bonus. Stable source releases are available on the main GNU download server (HTTPS, HTTP, FTP) and its mirrors; please use a mirror if possible. gzip reduces the size of the named files using Lempel-Ziv coding (LZ77). Whenever possible, each file is replaced by one with the extension ‘.gz’, while keeping the same ownership modes, access, and modification times. (The default extension is ‘z’ for MSDOS, OS/2 FAT, and Atari.) If no files are specified, the standard input is compressed to the standard output.Starting Price: Free -
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Platforma
MiLaboratories
Platforma is a no-code bioinformatics software that converts raw next-generation sequencing (NGS) data into insights. It offers a user-friendly interface with modular, no-code "blocks" for complex analysis tasks like immune repertoire, single-cell, and gene expression data. Building on the legacy of its predecessor, MiXCR, Platforma also enables AI-powered selection for antibody/TCR candidates. The platform is designed to be accessible to scientists without a bioinformatics background, allowing for scientists to take control of their own discoveries and reduce time to insight. -
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g.nome
Almaden Genomics
g.nome, a cloud-native platform that delivers streamlined, scalable, and interoperable workflows for next-generation sequencing analysis. g.nome provides a low-code/no-code pipeline build. With pre-built workflows and toolkits from a curated library, g.nome is giving power to researchers — enabling them to import custom code, handle big datasets reliably, and optimize team collaboration from anywhere. With g.nome, long-time barriers linked to workflow language, process flow visibility, and quality control are removed. All that’s left are streamlined, scalable, and interoperable genomic workflows — leaving research teams to do what they do best: focus on the science. -
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hc1
hc1
Founded to improve lives with high-value care, hc1 has emerged as the leader in bioinformatics for precision testing and prescribing. The cloud-based hc1 High-Value Care Platform® organizes volumes of live data, including lab results, genomics, and medications, to deliver solutions that ensure that the right patient gets the right test and the right prescription. Today, the hc1 Platform powers solutions that optimize diagnostic testing and prescribing for millions of patients nationally. To learn more about hc1's proven approach to personalizing care while eliminating waste for thousands of health systems, diagnostic laboratories, and health plans, visit www.hc1.com. -
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marimo
marimo
A reactive notebook for Python — run reproducible experiments, execute as a script, deploy as an app, and version with git. 🚀 batteries-included: replaces jupyter, streamlit, jupytext, ipywidgets, papermill, and more ⚡️ reactive: run a cell, and marimo reactively runs all dependent cells or marks them as stale 🖐️ interactive: bind sliders, tables, plots, and more to Python — no callbacks required 🔬 reproducible: no hidden state, deterministic execution, built-in package management 🏃 executable: execute as a Python script, parametrized by CLI args 🛜 shareable: deploy as an interactive web app or slides, run in the browser via WASM 🛢️ designed for data: query dataframes and databases with SQL, filter and search dataframes 🐍 git-friendly: notebooks are stored as .py files ⌨️ a modern editor: GitHub Copilot, AI assistants, vim keybindings, variable explorer, and moreStarting Price: $0 -
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VSClinical
Golden Helix
VSClinical allows for the clinical interpretation of variants based on ACMG & AMP guidelines. The VSClinical guided workflow enables following the American College of Medical Genetics (ACMG) guidelines used to identify and classify causal variants for inherited disease risk, cancer predisposition, and the diagnosis of rare diseases. The ACMG/AMP joint guidelines for variant interpretation provide a set of criteria to score variants and place them into one of five classification tiers. Following the guidelines requires deep diving into the annotations, genomic context, and existing clinical assertions about every variant. VSClinical provides a tailored workflow to score each relevant criterion while also providing all the bioinformatic, literature and evidence from clinical knowledgebases to assist in the scoring and interpretation process. VSClinical is designed to allow variant scientists to efficiently process variants. -
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Eidogen-Sertanty Target Informatics Platform (TIP)
Eidogen-Sertanty
Eidogen-Sertanty's Target Informatics Platform (TIP) is the world's first structural informatics system and knowledgebase that enables researchers with the ability to interrogate the druggable genome from a structural perspective. TIP amplifies the rapidly expanding body of experimental protein structure information and transforms structure-based drug discovery from a low-throughput, data-scarce discipline into a high-throughput, data-rich science. Designed to help bridge the knowledge gap between bioinformatics and cheminformatics, TIP supplies drug discovery researchers with a knowledge base of information that is both distinct from and highly complementary to information furnished by existing bio- and cheminformatics platforms. TIP's seamless integration of structural data management technology with unique target-to-lead calculation and analysis capabilities enhances all stages of the discovery pipeline. -
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Geneious
Geneious
Geneious Prime makes bioinformatics accessible by transforming raw data into visualizations that make sequence analysis intuitive and user-friendly. Simple sequence assembly and easy editing of contigs. Automatic annotation for gene prediction, motifs, translation, and variant calling. Genotype microsatellite traces with automated ladder fitting and peak calling and generates tables of alleles. Beautiful visualizations of annotated genomes and assemblies are displayed in a highly customizable sequence view. Powerful SNP variants analysis, simple RNA-Seq expression analysis, and amplicon metagenomics. Design and test PCR and sequencing primers and create your own searchable primer database. Geneious Biologics is a flexible, scalable, and secure way to streamline your antibody analysis workflows, create high-quality libraries and select the optimal therapeutic candidates.Starting Price: $1,280 per year -
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Geneyx
Geneyx
Geneyx Analysis is a comprehensive solution for next-generation sequencing (NGS) data that can scale the process of FASTQ to clinical reports for hospital and commercial labs. This advanced platform integrates machine learning and AI-based features to identify novel biomedical insights, while also improving diagnostic yields and turnaround times. By providing a fully transparent and intuitive solution, Geneyx Analysis enables clinicians and researchers to have complete control over data analysis and alleviates the complexities of regulating in-house bioinformatics pipelines. Protocols can be fully customized to accommodate gene panels, exomes, and genomes, and our comprehensive annotation engine supports the analysis of all genetic variants including structural and copy number variations as well as regulatory elements. Together, Geneyx Analysis automates the diagnostic process from sequencer to report, while creating a comprehensive resource for novel variant discovery. -
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BaseSpace Sequence Hub
Illumina
Data management and simplified bioinformatics for labs getting started and for rapidly scaling next-generation sequencing (NGS) operations. As a key component of the BaseSpace Suite, BaseSpace Sequence Hub is a direct extension of your Illumina instruments. Encrypted data flow from the instrument into BaseSpace Sequence Hub, enabling you to manage and analyze your data easily with a curated set of analysis apps. BaseSpace Sequence Hub is powered by Amazon Web Services (AWS). Offers a security-first environment. Enables you to set up runs and monitor instrument run quality. Promotes efficiency by converting sequencing data to a standard format and streaming directly to the cloud. Provides access to computing resources without the capital expenditure of in-house infrastructure. Increases organizational productivity with easy access to a multitude of genomic analysis apps (provided by you, Illumina, or third parties). -
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Microsoft Genomics
Microsoft
Instead of managing your own data centers, take advantage of Microsoft's scale and experience in running exabyte-scale workloads. Because Microsoft Genomics is on Azure, you have the performance and scalability of a world-class supercomputing center, on demand in the cloud. Take advantage of a backend network with MPI latency under three microseconds and non-blocking 32 gigabits per second (Gbps) throughput. This backend network includes remote direct memory access technology that enables parallel applications to scale to thousands of cores. Azure provides you with high memory and HPC-class CPUs to help you get results fast. Scale up and down based on what you need and pay only for what you use to reduce costs. Tackle data sovereignty requirements with a worldwide network of Azure data centers and adhere to your compliance requirements. Easily integrate into your existing pipeline code using a REST-based API and simple Python client. -
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ARES Touch
Graebert
ARES Touch is a comprehensive mobile CAD solution for iOS and Android devices, enabling users to create and modify DWG drawings on tablets and smartphones with a full suite of 2D drafting and annotation commands. Optimized for touch inputs, it allows field workers to access, annotate, and synchronize drawings in real time, ensuring they always work with the latest versions. Users can view, annotate, and modify DWG files on the go, making it ideal for technical surveys, on-site inspections, maintenance, project coordination, client meetings, and facility management. It supports synchronization with popular cloud storage services like Dropbox, Box, iCloud, Google Drive, and OneDrive, allowing offline access when needed. It offers a complete set of 2D drafting tools, including precise drawing aids such as the loupe, entity snap, tracking, and coordinate input. Additionally, ARES Touch enables users to annotate drawings with pictures taken from the device's camera and text legends.Starting Price: Free -
38
Bioconductor
Bioconductor
The Bioconductor project aims to develop and share open source software for precise and repeatable analysis of biological data. We foster an inclusive and collaborative community of developers and data scientists. Resources to maximize the potential of Bioconductor. From basic functionalities to advanced features, our tutorials, guides, and documentation have you covered. Bioconductor uses the R statistical programming language and is open source and open development. It has two releases each year and an active user community. Bioconductor provides Docker images for every release and provides support for Bioconductor use in AnVIL. Founded in 2001, Bioconductor is an open-source software project widely used in bioinformatics and biomedical research. It hosts over 2,000 R packages contributed by over 1,000 developers, with over 40 million downloads per year. Bioconductor has been cited in more than 60,000 scientific publications.Starting Price: Free -
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WS Grid+
WizardSoft
WS Grid+ is an accessible window manager for Windows 10. It helps you make order out of many chaotic program windows scattered across your screen. It lets you move and/or resize the active window using a grid selection system. It also provides keyboard/mouse shortcuts to instantly move and resize a window with no need to reach for its title bar. Finally, it gives you useful shortcuts to the Windows 10 virtual desktops feature. Double-tap key CTRL (or ALT + F1) to open/move the panel at/to the current mouse pointer's location. Use the mouse to make a grid selection. The active application window will duplicate the chosen relative position and size. Press CTRL while clicking on a grid cell to only change the window's position and leave its size as-is. Press the key ESC to close the panel (no focus needed). Resize the active window to preset dimensions and reposition to make it completely visible if needed.Starting Price: $6.72 one-time payment -
40
BarCodeWiz OnLabel
BarCodeWiz
Add barcodes to Microsoft Office with one click. Create a single barcode, pages of labels, or mail merge documents in Microsoft Word. Convert cells to barcodes or full sheets of labels directly in Excel. Easily create auto-incrementing barcodes. Add barcodes to your to your Access Reports. Choose from 23 types of barcodes, both linear (1D) and 2D. Compatible with all versions of MS Office from 2000 to 2016 and Windows 2000 to Windows 10. Create barcodes in any program supporting TrueType Fonts. Create single barcodes, pages of labels, or mail merge documents in Microsoft Word with the included add-in. Convert cells to barcodes or full sheets of labels directly in Excel using the included add-in. Create auto-updating barcodes by using Excel formulas. Add barcodes to your to your Access Reports. Add barcodes to Crystal Reports with the included User Function Library. Barcodes are created as text. Copy and paste to any document or program where text is supported.Starting Price: $149 one-time payment -
41
Pluto
Pluto Biosciences
Since its founding in 2021 from the Wyss Institute at Harvard University, Pluto has become a trusted partner of life sciences organizations around the country ranging from biotech start-ups to public biopharma companies. Our cloud-based platform gives scientists the ability to manage all of their data, run bioinformatics analyses, and create interactive and publication-quality visualizations. The platform is currently being used for a wide variety of biological applications, from preclinical / translational science research, to cell and gene therapies, drug discovery and development, to clinical research. -
42
Maple Flow
Maplesoft
Maple Flow is a mathematics tool that makes it easy for engineers to brainstorm, develop, and document their design calculations. Combining a simple, freeform interface with a comprehensive math engine, Maple Flow provides a whiteboard-style environment that automatically keeps calculations live as users refine, reposition, and develop their work. Do calculations, write documentation and easily refine your work in an environment that does not feel like a programming tool or a spreadsheet. Place math, text, images, or plots wherever you wish, and reposition your work with the mouse or keyboard – Maple Flow keeps everything organized behind the scenes. Maple Flow contains all the powerful features that technical professionals expect in a calculation tool, with fast solvers, built-in units tracking, flexible plots, and more. -
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CSAM ProSang
CSAM
CSAM ProSang is an advanced Laboratory Information Management System (LIMS) that simplifies the entire management of blood, cells and tissues, from donation to transfusion or transplantation. It is used in five countries, at more than 180 blood centers in 26 healthcare regions. CSAM ProSang’s comprehensive functionality includes all aspects of blood donor management, administration, production and analysis, allocation and delivery of blood for transfusion. It uses the same proven process for stem cells, organ transplantation and tissue management. The system also handles immunological exams, including immunogenicity and tissue-type serology. From the time a sample is taken from the donor, through the production, analysis and delivery to the recipient, CSAM ProSang tracks ever step via barcode labeling. The system’s advanced barcode technology automatically recognizes and alerts users if the incorrect blood, cell or tissue is scanned. -
44
jPDFViewer
Qoppa Software
Integrate a PDF reader right into your Java application or website. jPDFViewer is a self contained Java component that can be deployed in a Java application or a web application (in a web page as an applet, or a Java webstart application). Since it is written in Java, it allows your application to remain platform independent and run on Windows, Mac, Linux and Unix. jPDFViewer can load documents from files on a local or network drive, from a URL and from Java input streams for documents that are generated runtime or come from other sources, such as a database. Main Features: Read and display PDF files on any platform that supports Java Print PDF files Fill interactive PDF forms View all markup annotations Validates and displays digital signatures Text search and selection Advanced tools: zoom, loupe, snapshot, pan and zoom Easy navigation with different views: thumbnails, bookmarks, annotations... Customizable toolbar and user interface Support for all image typesStarting Price: $2,000 -
45
CDR Analyzer
S.K. Infotech
CDR (Call Detail Records) Analyzer is a reporting tool which is used for analyzing various types of CDRs such as Single Number CDR, Multiple Numbers CDR, Single Tower CDR and Multiple Tower CDR. This software gives output data in many formats. We can get addresses of cell Ids directly. Single Number CDR: common caller, cell ID target number, filter time, filter date, filter number, first and last call, multiple cells ID, number cell ID, same IMEI different IMSI number. Multiple backup and restore facility, network access, advance search facility, (2 level passwords). -
46
TreeGrid SpreadSheet
COQsoft
TreeGrid SpreadSheet provides cell based AJAX grid with spreadsheet features like editable formulas, many predefined and custom formula functions, individual cell styling and borders, manipulating individual cells or selected cell groups, auto grid size, auto row and column index. Dynamic cell styling - every cell can have set and changed style attributes: text color, background color, shadow color and style, font size and name, text bold, italic, underline, strike, overline and small caps. And also horizontal and vertical alignment, wrapping text vertically and text rotate 90 and 270 degrees. Dynamic cell span - every cell can be vertically and horizontally spanned through more next cells. Dynamic cell format - every cell can have set and changed its type and display format.Starting Price: $200 per device -
47
Hex
Hex
Hex brings together the best of notebooks, BI, and docs into a seamless, collaborative UI. Hex is a modern Data Workspace. It makes it easy to connect to data, analyze it in collaborative SQL and Python-powered notebooks, and share work as interactive data apps and stories. Your default landing page in Hex is the Projects page. You can quickly find projects you created, as well as those shared with you and your workspace. The outline provides an easy-to-browse overview of all the cells in a project's Logic View. Every cell in the outline lists the variables it defines, and cells that return a displayed output (chart cells, Input Parameters, markdown cells, etc.) display a preview of that output. You can click any cell in the outline to automatically jump to that position in the logic.Starting Price: $24 per user per month -
48
Teleprompter Mirror
Teleprompter Mirror
Teleprompter software allows you to read your lines quickly and without mistakes. Choose between automatic scrolling and voice-activated scrolling, which follows your voice as you talk. Multilingual support--you can use non-English characters, even Kanji. Font color and images are enabled. With this mode on, you can write your teleprompter script in another program such as Word or another editor, then copy/paste it into this screen with your formatting preserved. In addition to running on a desktop PC, the software automatically adjusts to your screen size on smaller devices. When editing your script on cell phones and tablets, you'll find it helpful to sync a bluetooth keyboard or plug it into the USB port of your cell phone, tablet, or iPad. Adding a touchpad keyboard or mouse makes it even easier to edit your script. -
49
IRI CellShield
IRI
IRI CellShield® protects the sensitive information in your Microsoft Excel® spreadsheets, allowing you to comply with data privacy laws. Point-and-click to protect your columns with reversible and non-reversible masking functions. CellShield keeps your data secure, whether it's in one sheet or a million. Use multiple search methods to find and report on PII across the LAN, and protect it all at once. Classify and mask it in intuitive graphical dialogs. CellShield's core technology is built on the award-winning IRI FieldShield data masking product for databases and flat files. Data masked in one platform can be revealed in another. CellShield EE is the only full-featured, professional data discovery, masking, and auditing package for Excel 2010, 2013, 2016, and 2019 (plus Office 365) workbooks in your LAN. CellShield EE exceeds the security and scope of a single password by combining and automating all these extra capabilities.Starting Price: $35 one-time payment -
50
think-cell
think-cell Sales
think-cell helps you create stunning charts in minutes, boosts your slide layout, and automates your regular reports. And all this with a single PowerPoint add-in. All functions are available right in the PowerPoint objects. think-cell avoids such clutter and has a simple user interface. think-cell uses only native PowerPoint charts and shapes for its output. Charts created with our software and shared with pure PowerPoint users remain data-driven and changeable. And should you ever decide to stop using think-cell, all your slides and charts will remain available and changeable as if you had created them with standard PowerPoint. It is a powerful charting and layout software that automates your PowerPoint work, improving slide creation efficiency and quality. Within minutes you get well-laid-out and great-looking slides. Excel-based datasheet with formulas. Absolute & percent difference arrows. Percentages derived from absolute values. A table-like layout of series legends.Starting Price: $19.90 per month
