Alternatives to hc1

QUALO is an adaptable cloud-based software platform designed to tackle prevalent data output and visualization challenges in the areas of behavioral health, community health, and healthcare. The system's primary goal is to offer valuable insights without overwhelming stakeholders, including clients, staff, administrators, and funders. QUALO combines data collection tools with customized evidence-based practice supports, ensuring the precise capture of pertinent information at the right moment. Additionally, it incorporates specialized care coordination features tailored explicitly for the requirements of human service providers. One of QUALO's key strengths lies in its seamless integration capability with various systems, notably electronic health records (EHRs). Acting as a singular data entry point, it works to enhance the limitations often inherent in EHRs' data output and visualization. Moreover, QUALO's mobile-friendly design enables universal access across different devices, thereby streamlining the entire data collection process for enhanced efficiency.

MedRight is a user-friendly, fully supported, cost-effective EHR/eMAR that can be used in senior living communities such as ALFs, and SNFs. Because of its flexible configuration features, other users include IDDs, and treatment centers). MedRight is HIPAA compliant and ensures patient safety. MedRight is used coast to coast and includes all the features needed to manage any senior living community: Inventory Tracking e-Naarcotic Logs eMAR Full reporting Seizure Tracking Behavior Tracking Charting Incident Tracking Manage Staff and Residents Assessments Care Plans Community Calendar Resident Calendar Vital Tracking and Graphing e-Prescribing Refusal Log Text/email notifications Document Manager Alerts and Trends Pharmacy Integration Ability to work without internet Standing Orders email blasts to resident families Family Portal CRM specific for your usage ADL tracking Wound management Staff License and Training Management Dashboard to track Key Performance Indicators (KPI) Web-based and on the Cloud We integrate with other health care providers using our API and strongly believe in healthcare interoperability. Get a demo or try MedRight's free trial.

AZZLY Rize is the premier clinical and business platform for addiction treatment and mental health organizations. As a modern technology platform, AZZLY Rize is a system that can scale with you. Use as little or as many of the features and functions available based on your program and staff needs. Key features for OUTPATIENT Programs include e-check-in, scheduling, appointment reminder, Zoom telehealth, treatment plans, progress notes, assessments and surveys. For RESIDENTIAL Programs: census, medication management, bed board, withdrawal management, DrFirst e-prescribing, EPCS, PDMP and labs. For all Programs: alerts, patient engagement, 5 star implementation and support services, and seamless electronic billing and claims submission. As a true all-in-one platform, we empower treatment centers to take control of their compliance and revenue cycle management and reporting requirements. As a purpose-built tool for mental health and substance use disorder programs, we offer a flexible pricing plan to replace dated technology. Use our compliant Master Library of Forms or we configure your documentation forms to match what you use today. Hosted in Microsoft Azure Private Cloud Network for added security and HIPAA privacy.

This powerful tool allows you to practice medicine anywhere and anytime. The athenaOne mobile application allows you to do meaningful clinical work wherever and whenever you want. Access patient records to create and sign orders, respond and prepare for exams, and to document them. The app allows you to catch up on work or get ahead of it during your free time. You can log in to the app with touch or face ID to see a quick overview of your day. You can view your schedule, see the patients you have prepared for, and manage your inbox. With customizable patient summaries, it takes just a few minutes to get up-to date on the patient's history. To review all that has happened since their last visit, you can access full charts. Access the clinical inbox for critical work from anywhere and at any time. AthenaClinicals makes it easy to create and sign orders, view test results and respond to patient cases.

Connect care teams seamlessly to a 360-degree view every patient on one HIPAA-compliant platform. Transform your call center, connect patients to care quickly, and take action on social determinants to improve outcomes. A streamlined engagement platform connects people, data and processes to help patients acquire, support, engage, and engage them throughout their journey to health. Transform virtual sales, provider relationships, patient engagement, and other activities to increase value and drive results. Connecting sales, service, and marketing with critical data will help you achieve commercial excellence. Meet your constituents right where they are. Staff can make the best decisions with insight-driven processes that give them a 360-degree overview of the families and individuals they serve. Your team can quickly respond to any healthcare emergency by providing manual contact tracing, patient monitoring and automated follow-ups.

The fastest-growing remote patient monitoring platform and the only one that is completely free for you and your patients. 100Plus can monitor more conditions such as heart disease, low/high cholesterol, diabetes, and weight. It is the easiest to implement -- you can be up and running in just minutes and have devices shipped directly to your patients' doors. 100Plus offers White-Glove enrollment -- onboarding 10 or 10,000 patients. It also provides outreach and education to patients quickly. 100Plus' Predictive Population Health Management™ continuously monitors the health of your patients and sends alerts to you for intervention and prevention. 100Plus integrated cellular without monthly plans or bill devices includes: Blood Pressure Cuff and Blood Glucose monitor, Digital Weight Scales, Emergency Watch, Digital Thermometer and Pulse Oximeter. We offer: - White Glove set up (patient outreach, education and enrollment). Product support via phone or online chat available between 9am and 9pm ET

myUnity®, - Leveraging the most strategic elements of the Netsmart market-leading senior living, hospice, and home care solutions into a unified enterprise platform. All your post-acute care settings can be accessed from a single location or across hundreds. It is user-friendly and gives your clinical staff the right information at the right moment so they can concentrate on patient care. This platform is designed to provide value-based care through connectivity, analytics, population health management and electronic referral management.

Ampersand Health provided an 8-week support program for IBD patients who suffer from chronic pain and fatigue. The average ACT survey score of the patients who completed the program significantly improved (n=21; p0.0001). The programme helped participants to accept and improve their psychological flexibility, learn more about chronic symptoms, feel less alone, and live a fulfilled life despite continuing pain and fatigue. The study found that fatigue and chronic pain levels did not change as expected. The programme had a positive impact on symptoms perceptions, according to self-reported data. The trial was able to measure symptoms and disease activity using a validated Patient Report Outcome Measure.

ShiftCare's Care Management features make it easier to provide highly personalized support to clients, their families, and their families. Our care management features make it easy to organize shifts, rosters, and teams, allowing you to deliver a more efficient and effective service. ShiftCare seamlessly integrates timesheets, expenses, and invoices to make accurate accounting easy. This will reduce your workload and help you grow. We connect you and all your teams with everything you need to coordinate shifts, coordinate clients, and provide quality care wherever they are. We make it easy for new clients to be welcomed, understand their needs and manage their goals. We also help them establish good relationships with their family and friends. Your teams will support clients in reaching their goals. We make it easy to track their progress and share it with the right people.

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 for PCR and sequencing and design and test them. Geneious Biologics offers a flexible, scalable and secure way to streamline antibody analysis workflows. It allows you to create high-quality libraries, and select the best therapeutic candidates.

Livindi uses sensors and Artificial Intelligence to notify of any changes in the bathroom, eating or sleeping habits, as well as overall activity. The button will send a message to each member of the care team. It also monitors movement. It can detect potential falls based upon changes in behavior and does not require a wearable. Monitor blood oxygen level, temperature and weight as well as respiration rate and HRV. You will be notified when someone gets in and out of bed. You can track medications and have instant access to the Livindi Concierge. To start a video chat, tap on a face. Autoanswer makes it easy to answer questions without having to do anything. You can share pictures and videos that will automatically appear on your LivindiPad tablet. Closed captions are available for video calls to assist those who are hard of hearing. Livindi can be yours by tomorrow, and you don’t even need an Internet connection. Fellowship Senior Living and Livindi are teaming up to offer affordable services for older adults.

ResiDex Software offers an innovative, integrated, and user friendly software solution for your Adult Day Services, Group Home, or Assisted Living center. ResiDex allows users to manage client demographics, coordinate medications, and other critical data related to the care of clients and residents. ResiDex Software's intuitive design makes it easy to use, from data entry through data analysis and everything in between! Our customer support is unmatched.

We assist healthcare providers in orchestrating care continuum pathways and improving the experience of patients and providers. Our digital transformation moonshot aims to create a human-centric healthcare ecosystem that improves the provider-patient relationship and changes the patient experience. Our proprietary software platform and extensive solution portfolio enable us to provide seamless orchestration and superior convenience for patients, physicians, and other providers.

High-value decisions can be made and cross-functional collaboration within the care system can be enhanced. The Incedo™, Healthcare Management Platform is a complete medical management solution that seamlessly integrates utilization management, care coordination, health care navigation interventions, and care management to improve operational efficiencies. Facilitate communication between Care Management, Clinical, and Utilization Management teams by sharing a member care plan. This allows for easy transition between UM/CM. Enhanced Data Capabilities - A flexible data repository that can be customized for granular tracking and reporting simplifies data capture and CMS compliance.

The award-winning XIFIN LIS, a SaaS-based laboratory information platform, is fully scalable and scalable. It offers flexible and secure connectivity, multi-specialty workflows and cutting-edge capabilities to optimize complex and high volume testing labs. The healthcare industry is changing to accommodate patient-centered and value-based coordinated care models. The rapid adoption of next-generation sequencing (NGS) and genomic testing is accelerating this shift. Laboratories will need to adapt their processes to meet the challenges of reporting and implementing these complex tests. Diagnostic insights can help reduce healthcare costs and improve patient care. It is therefore crucial that laboratories integrate better with the healthcare system. These demands drive greater interaction and communication among all healthcare and diagnostic providers.

Geneyx Analysis provides a comprehensive solution to analyze next-generation sequencing data. It can be used by commercial and hospital labs. This advanced platform integrates AI and machine learning features to identify new biomedical insights while improving diagnostic yields. Geneyx Analysis provides a transparent and intuitive solution that allows clinicians and researchers complete control over their data analysis. This reduces the complexity of regulating internal bioinformatics workflows. Our comprehensive annotation engine can support the analysis of all genetic variations, including structural and copy-number variations, as well as regulatory components. Protocols can also be fully customized for gene panels, genomes, or exomes. Geneyx Analysis automates diagnostics from sequencer to report while creating a comprehensive resource of novel variants.

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.

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.

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.

We help healthcare systems reduce their burden by providing automated analysis, diagnosis and treatment solutions to healthcare professionals and patients around the world. Congenica was founded by pioneering work done at the Wellcome Sanger Institute in the UK and the NHS. Our products combine the latest technology, automation and AI to create a platform that is uniquely differentiating. This platform can be used in any area of human disease, where genomic data is critical to unlocking actionable insight. We are a digital healthcare company that provides software and solutions to analyze and interpret genomic data at large scale. Full automation using powerful APIs and ML, to reduce the burden of specialist staff, increase case throughput, speed up decision-making and streamline reporting. Platform for accurate, certified, and secure clinical decision support with the highest level of confidence in clinical outcome.

Your agency and sales team can access real-time market information and sales insights right from their fingertips. Target referral sources based upon their patient mix and discharge patterns, and add them to the pipeline. Target referral sources based upon their patient's discharge patterns and clinical groupings. Compare readmission performance, payer mix breakouts, and diagnosis level metrics to see where your agency stands. With customizable dashboards and reports for reps and teams, you can optimize sales efforts and increase close rates. You can nurture referrals and strengthen relationships by providing detailed customer profiles and guided discussion points via your mobile device. To help hospice patients receive better care, empower hospice sales teams with data-driven clinical metrics and predictive clinical metrics. To determine if hospice is worth their time, drill-down, uncover and benchmark hospice patients using clinical treatment demographics, care insights, and benchmarking.

Empowering patient consumers to triage their care to the right services and care. We help providers and health systems acquire new patients and keep existing patients by providing a better, more consumer-centric experience. We help improve patient engagement and outcomes. We offer plan members self-service symptom check, triage, and step by step guidance to help them find the most suitable, convenient, cost-effective and trusted in-network healthcare. We work with digital health, healthcare innovation and healthcare SaaS companies in order to enhance digital products with clinically-validated AIchat solutions.

HQ3 is a web-based application that allows you and your team to market multiple health services. It has many great features that doctors and pharmacists have requested. With a click of a button, you can set preferences to make HQ3 work exactly how you want it to. HQ3 can help you expand your services while providing exceptional patient care. HQ3 is built for success, and it's easy to get started with HQ3. Before you go live, our support team will make sure everything is in order.

They are large-scale healthcare providers and must collect, store, analyse, or interpret patient information in a smart manner to ensure high-quality patient care. What happens if all these practices are made automotive? Yes. The perfect healthcare management system, Health360 eMedical, is the ideal digital partner for all-scale healthcare professionals such as doctors, pharmacists, and others to improve their workflow and ensure that patients receive effective care. No matter what healthcare platform you use, digitization can now be observed everywhere. With its dedicated dashboards, and the impressive features that are available for professionals on these platforms, our health360 product perfectly fits all of them. eMS allows for the management of patient data, inventory and monitoring of medical team activities via a web interface.

The QIAGEN CLC Geneomics Workbench is a powerful tool that works for all workflows. It is easy to overcome data analysis challenges with cutting-edge technology, unique features and algorithms that are widely used by scientists in industry and academia. Bioinformatics software solutions that are user-friendly allow for comprehensive analysis and interpretation of your NGS data. This includes de novo assembly and transcriptome assembly, resequencing analysis, WES and targeted panel support, variant calling, variant calling, RNA–seq, ChIP–seq and DNA methylation analysis (bisulfite sequence analysis). You can analyze your RNA-seq (miRNA, smallRNA) and smallRNA (lncRNA), data using easy-to-use transcriptomics workflows that allow for differential expression analysis at both gene and transcript levels. QIAGEN CLC Genomics Workbench was designed to support a wide variety of NGS bioinformatics programs.

Welkin is designed for care coordination. You need to assign the right person to take care of patients at each step of the journey. We offer seamless transitions for your team members and a personalized experience for each patient they serve. Automating any program can increase patient engagement, reduce task burden, and seamlessly move patients into the next phase. Your team can focus on what they do best, which is providing care by defining processes and escalations that are based on outcomes. You can create escalation paths for events that require monitoring, such as adverse events, out of-range results, patient responses, and lack of engagement. Automate internal alerts or trigger emails or SMS to care staff members based upon an action or inaction, upcoming appointments, missed appointments, or other factors.

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.

The most comprehensive and configurable digital health solution for healthcare providers. Manage your community, increase repeat visits, video consultations, and increase Pharmacy & Diagnostic revenue. NHCircle lets healthcare providers manage their relationships with their patients outside of their own premises. It connects all stakeholders in the care team, ensuring seamless care for patients.

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.

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.

Alissa Interpret provides a universal software solution for the interpretation of genomic data in clinical decision support. Alissa Interpret is a platform that can be used for CGH or NGS tertiary analyses. It will increase your productivity, reduce turnaround time and maintain regulatory compliance. Alissa interpret, Agilent's SureSelect NGS reagents and intuitive Alissa Reporter for secondary NGS analysis, Magnis walkaway automated, and TapeStation QC will help you achieve complete operational efficiency. You can access external and internal variant knowledgebases. Automated variant analysis solution accelerates CGH/NGS tertiary analyses. SNVs and InDels are all handled by the same platform. CNVs, LOHs, fusions, CNVs and InDels can also be analyzed. Integrate with your LIMS to eliminate bottlenecks in genomic data analysis. Connect with peers to share knowledge and improve diagnostic yield.

Administrators, Doctors, Receptionists and Laboratory staff all have one easy-to-use management software. Health.NET is a desktop solution that uses SQL Server Database and runs on Microsoft Windows 7/8/10 computers. Services and web modules are written in Java and Ajax. Health.NET is suitable to all healthcare and medical environments. The CORE version allows you to manage your patient archive, medical record, billing management, professional reports and visits, as well as prescriptions management. This software is ideal for specialists, doctors, and medical groups. One software solution that allows you to share and protect medical data as well as administer it. Health.NET Ultimate adds advanced modules to CORE and provides a responsive service for patients, employees, and administration. It is easy to set up and maintain, and assists users in all aspects of a laboratory workflow, from sample registration to management.

VSClinical allows the clinical interpretation based on ACMG & AMP Guidelines. The VSClinical workflow is guided by the American College of Medical Genetics guidelines for identifying and classifying causal variants in inherited disease risk, predisposition to cancer, and diagnosis of rare diseases. The ACMG/AMP Joint Guidelines for Variant Interpretation provide a set criteria to score variants, and place them in one of five classification tiers. The guidelines require a deep dive into the annotations and genomic context of each variant, as well as existing clinical assertions. VSClinical offers a customized workflow to score each relevant criteria, while also providing bioinformatics, literature and evidence gathered from clinical knowledgebases. VSClinical was designed to help variant scientists process variants efficiently.

Bridge is an award-winning enterprise solution for patient engagement in healthcare organizations. The platform allows companies replace their existing EHR's Patient Portal, connect multiple IT systems, consolidate patient engagement tools, launch a digital frontdoor, and connect multiple health IT system. The solution is easy to deploy and scaleable. It is ONC 2015 Edition Certified. It can be downloaded as a web application for clients and a mobile app for Android or iOS. Bridge automates the entire care process, simplifying the patient experience. With customizable electronic communications and access to financial, health, and appointment information on multiple platforms, patients are kept informed and engaged. You can schedule your own appointments, access to health information, secure patient-provider messaging and mobile intake. Bill pay is also available. Healthcare organizations can create their own interfaces and add-on features using a fully-documented API. They can also run advanced reports with the API.

Everything you do is influenced by providing the best patient care. We empower it with tools that simplify your team's workflows, digitize data, and provide the right clinical documentation to the right people at the right times. Forcura is the clinical workflow solution of choice for top healthcare organizations. It can manage care transitions and coordinate care across your teams. Forcura consolidates referrals coming from multiple sources into one location. This allows your team to track, track, and respond to any referrals. Home healthcare teams can connect, so they can work from anywhere with a web connection. With faster patient onboarding and efficient workflows, every second counts. Automated technology can streamline patient referrals and accelerate billing cycles. Digital workflows and patient-centered tools can reduce operating costs.

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).

Software for fast, simple, and repeatable analysis of variants in gene panels, whole genomes, and exomes. VarSeq provides an intuitive and integrated software solution for tertiary analyses. VarSeq allows you to automate workflows and analyze variations for gene panels, whole genomes, and exomes. Our software makes it easier than ever to understand genomic data. VarSeq is a powerful software that provides a powerful filtering engine and annotation engine for sifting through large variant data. You can narrow down your list of variants quickly by using a series of filters. You can save the filters you have created after you have determined the parameters that are most effective for your analysis. This allows you to easily apply the same analysis on another dataset. VarSeq is ideal for high-throughput environments because the same automated workflow can apply to each batch of samples. Real-time filtering allows you to quickly prototype and fine-tune analysis workflows.

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.

The toolkit was developed in the Data Sciences Platform of the Broad Institute. It offers a variety of tools, with a focus on variant detection and genotyping. Its powerful processing engine, high-performance computing capabilities and flexibility make it a great tool for any project. The GATK is a standard in the industry for identifying SNPs in RNAseq and germline DNA data. Its scope has now expanded to include somatic short variation calling, copy number (CNV), and structural variation (SV). The GATK includes not only the variant callers, but also many utilities that perform related tasks like processing and quality-control of high-throughput sequence data. It also bundles the Picard toolkit. These tools were designed primarily to process whole genomes and exomes generated by Illumina sequencing technology. However, they can be adapted for a variety other technologies and experimental design.

Real-time location systems (RTLS) provide real-time visibility to reduce waste and improve customer experiences. Infor®, Location Based Intelligence, is an interoperable platform for hospitals, clinics, and health systems that uses Real-Time Location Systems. This healthcare-specific solution gives real-time visibility into staff, patients, medical equipment, and staff movements. Location Based Intelligence works with the best RTLS hardware technology in order to offer the most comprehensive and cost-effective solution for client needs. Automatically tracking all interactions between patients and staff; sending notifications when assistance is required. Reduce bottlenecks, optimize patient flow, and optimize staffing resources to deliver better care. You can find and replenish equipment quickly, and you can monitor utilization data to make smarter rental and purchasing decisions.

Loupe Browser is an intuitive visualization software that allows you to explore and analyze 10x Genomics Chromium or Visium data. LoupeR can convert Seurat objects to Loupe Browser files. The Loupe Browser interface's navigation and interactive features are based on a dataset of lung squamous-cell carcinoma. The workspace is centered on the view panel, where single points representing barcodes of cells are shown in different projections. Each point represents a barcode. The vast majority of them correspond to a cell. The default projection, created by the Cell Ranger pipeline, is the tSNE plot. Other projections are also available. You can move the plot by dragging the mouse over cells. Zoom in and out using the mouse wheel or trackpad. Cluster labels will appear as you move the mouse over the plot. This is useful for data with a large number of precomputed groups.

Cufflinks assembles transcripts, estimates their abundances, and tests for differential expression and regulatory in RNA-Seq sample. It accepts aligned RNA Sequence reads and assembles them into a minimal set of transcripts. Cufflinks estimates the relative abundances for these transcripts by calculating how many reads each one receives, while taking into account biases from library preparation protocols. Cufflinks is the result of a collaboration between the Laboratory for Mathematical and Computational Biology. We provide binary packages for Cufflinks to make the installation process easier. This saves users the sometimes frustrating task of building Cufflinks which requires you to install the libraries. Cufflinks comes with a number tools for analyzing RNASeq experiments. Some of these tools are standalone, while others form part of a larger workflow.

AlphaMed Solutions includes electronic healthcare records, customized solutions, and modern healthcare and business applications that collect and analyze real time critical patient data. These HIPAA-compliant solutions use cutting-edge medical protocols and combine the expertise and experience of award-winning Alpha Software engineers with practicing physicians. The apps can access and collect medical data at high speeds, work with or without a cell signal and integrate with almost any healthcare system. For example, the AlphaMED Workplace Wellness app guides employees to the end of a COVID-19 quarantine period or illness period by collecting daily temperature readings and current symptoms. The app uses established criteria, test results, and the illness cycle to determine when key milestones have been met and alerts employees when they are safe to return to work.

Transformative technology and data insights will help care providers achieve better health outcomes. The future of community health care is connected and part a continuum that includes traditional and emerging care models. AlayaCare makes this personalized and predictive. We are determined to provide the care our loved ones deserve in the home they call home. Transformative technology and data insights will help care providers focus on the important things. This will enable them to achieve better health outcomes. The future of community health care is connected and part a continuum that includes traditional and emerging care models. AlayaCare makes this personalized and predictive. AlayaCare's unique platform provides a complete solution for managing the entire client lifecycle using a secure, integrated cloud-based platform.

Our global data-sharing networks generate clinically actionable insights to improve patient outcomes globally. SOPHiA GENETICS is on a mission to build the future in AI-assisted medical care. We are integrating multimodal data from healthcare-omics, unlocking existing data silos and developing machine learning models in order to produce actionable insight that can eventually support healthcare professionals improve patient outcomes. The new interface, features, and cutting edge capabilities will accelerate precision medicine workflows and bring us closer to democratizing the data-driven medicine.

One platform that allows operators to connect with patients and families, standardize compliance programs, provide mock surveys, reimbursement scrubbers, and many other features. We help you reduce software fatigue and consolidate all your operational needs under one roof. Our APIs and partner integrations make it easy for you to import and connect to your existing tools. Connect to your EHR or other patient data platforms to complete the patient data care loop. We offer baked-in features and services that you wouldn't need to purchase another software for. GreyMAR's toolkits can be used to improve your community's efficiency, image and security on multiple fronts. GreyMAR's emergency preparedness suite is specifically designed for healthcare. It will help you improve your organization's Disaster Recovery process (DR). Our powerful workspace builders will help you find more IPA opportunities. Create a tracker to add patients to an intelligent care plan.

Design and simulate cloning processes accurately. Test complex projects, catch mistakes before they happen, get the right constructs on the first try. Cloning becomes easier when you see what you're doing. The intuitive interface simplifies complex tasks by providing you with a clear view of your work. SnapGene automates the documentation so you don't need to. Share and view every sequence edit or cloning process that led to the final plasmid. Improve your core molecular biological procedures and your results. SnapGene Academy, our new online learning centre, will help you master SnapGene as well as key concepts in cloning. SnapGene Academy contains over 50 video tutorials, taught by experts in the field. This helps you improve your skills in multiple molecular biological courses. SnapGene 7.2 offers a new visualization for primer homodimer structure and enhancements to the file management. Tabs can be organized using drag-and-drop in multiple windows.

All skill levels are welcome. It is as easy as taking a photo of a wound using a smartphone. Clinicians can then evaluate the wound's health and create documentation for reimbursement. Keep wounds from getting worse and prevent readmissions to improve star ratings. To attract more patients, turn your success in wound care into a marketing tool. Accept more complex wound patients with confidence Swift believes that reimagined healthcare technologies will bring new levels to healthcare. They are designed with empathy and will allow for better clinical care. Smartphone cameras have exceeded their clinical utility. Healthcare on the planet needs new technologies to help it make the next big leap. Swift is the world's leading smartphone imaging platform. This allows patients to take high-quality clinical images anywhere they may be.

Founded in 2007, FieldSync is a company headquartered in the United States that creates software called FieldSync Health. FieldSync Health is a type of assisted living software, and provides features like billing & invoicing, electronic signature, employee tracking, patient intake, scheduling, and time / task reporting. The FieldSync Health software product is SaaS software. Product pricing starts at $49.99/month/user. FieldSync Health includes phone support support. Some competitors to FieldSync Health include Sevocity EHR, Livindi, and hc1.