Genohm is a software company that builds laboratory information management and data orchestration systems for genomics, diagnostics, and regulated laboratory environments. The platform centralizes sample metadata, instrument outputs, analysis results and audit trails so teams can manage high-volume workflows from sample intake to report delivery. Genohm is typically deployed in clinical sequencing centers, diagnostic labs, and biotech R&D operations where traceability, reproducibility and regulatory compliance are essential.
Genohm combines a configurable LIMS backbone with workflow automation, reporting, and integration adapters for laboratory instruments and bioinformatics pipelines. The system is designed to be configurable without extensive custom coding, enabling organizations to map their existing laboratory processes into the software while preserving auditability for ISO/GxP/GDPR requirements. Deployments commonly include a mix of on-premises and cloud-hosted components depending on data residency and performance needs.
Operational users include lab managers, molecular biologists, bioinformaticians and quality teams: lab staff use the UI for sample accessioning and instrument runs, bioinformatics teams trigger and monitor pipelines, and quality/regulatory users review audit logs and compliance reports. IT teams manage integrations to hospital information systems, LIMS connectors to sequencing instruments and identity management via SSO.
Genohm groups features around sample lifecycle management, workflow automation, data integration and compliance. Core capabilities include sample and container tracking, configurable workflows, automated instrument data capture, chain-of-custody audit trails, user and role management, and reporting. The product emphasizes flexibility: users can create custom forms, validation rules and pipelines without deep developer involvement.
Key components include a sample registry that stores structured metadata, an execution engine for sequencing or assay workflows, and a results repository that keeps processed data and reports tied to original sample records. The platform supports versioned configuration, allowing controlled changes to workflows and templates and supporting validation activities required by regulated labs.
Integration and extensibility features are prominent: the platform offers connectors for sequencing instruments and common laboratory hardware, APIs for automation and data extraction, and support for identity and access controls such as SAML/OAuth. Built-in audit logs, electronic signatures and configurable retention policies are included to support compliance frameworks and internal QA processes.
Genohm manages and automates laboratory workflows from sample accessioning through analysis and reporting. It captures instrument outputs, associates them with sample metadata, triggers downstream bioinformatics pipelines and consolidates results into traceable reports. This reduces manual data handling, decreases transcription errors, and speeds up turnaround times.
The platform also enforces process controls and captures immutable audit logs needed for regulatory compliance. For clinical or regulated uses, Genohm's configuration-driven approach lets labs implement controlled change procedures and document validation steps. The system can generate compliance-focused artifacts such as change histories, access logs and electronic sign-offs.
Finally, Genohm acts as a bridging layer between lab instruments, analysis tools and enterprise systems. It handles data format normalization, stores provenance information, and pushes finalized results to EMR/ERP systems or downstream reporting tools. That integration capability makes it useful for labs that need to deliver results into external clinical or business workflows.
Genohm offers these pricing plans:
Because Genohm typically serves regulated and enterprise customers, pricing often varies substantially based on deployment model (cloud vs on-prem), number of users, expected sample throughput, required integrations and validation support. For the most accurate and current information, check Genohm's enterprise services and contact channels on their website at https://www.genohm.com/.
Genohm starts at approximately $500/month for small pilot deployments billed as a Starter subscription. That entry-level band usually covers a small user base and limited sample volumes. Production-scale usage with full automation and connector support typically moves into the $2,000/month Professional band or higher and enterprise contracts are quoted based on scope.
Genohm costs approximately $6,000/year for the Starter tier when billed annually and around $24,000/year for the Professional tier, based on monthly-equivalent pricing. Enterprise customers usually negotiate annual contracts that include implementation, validation and support fees; final yearly costs depend on customization and SLAs.
Genohm pricing ranges from $0 (evaluation) to enterprise-level custom pricing. Small labs running pilot projects can expect low-to-mid four-figure annual spend, while larger clinical or high-throughput sequencing centers typically invest in mid-to-high five-figure annual contracts. Costs scale with the number of concurrent users, integration complexity, validation assistance and whether the deployment is on-premises or cloud-hosted.
Genohm is used to manage laboratory sample lifecycles, automate routine lab processes, capture instrument outputs and consolidate analysis results into auditable records. Primary use cases include next-generation sequencing (NGS) sample tracking, clinical diagnostics reporting, biobanking metadata management, and R&D workflows where sample provenance and reproducibility matter.
Clinical and diagnostic labs use Genohm to ensure end-to-end traceability of patient samples, support ISO/GxP compliance, and produce final results that can be exported or transmitted to hospital systems. Research groups and biotech companies use the platform to coordinate multi-step experimental workflows, reduce manual data handling, and integrate bioinformatics pipelines.
Operational benefits include reduced human error through automation, faster turnaround via pipeline orchestration, clearer audit trails for compliance reviews, and centralized data that supports downstream analytics and business intelligence. The system also facilitates collaboration between lab technicians, bioinformaticians and quality personnel by providing a single source of truth for sample and result data.
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Operational considerations include change control, validation documentation and training — all critical for regulated labs and commonly handled as part of Genohm's enterprise onboarding services.
Genohm typically offers evaluation access or a pilot program to let labs validate the platform against their workflows. These pilots usually include temporary credentials, a sandbox instance preconfigured for sample intake and a limited number of instrument connectors so labs can test integrations and process flows. Pilots are useful for demonstrating fit with existing bioinformatics pipelines and for estimating data volumes and performance behavior.
Pilot programs are commonly limited in duration (for example 30–90 days) and capacity; they are designed to let teams validate workflows and produce proof-of-concept results before committing to full deployment. For regulated projects, pilots also help define the validation plan and identify configuration items that will require formal testing.
To arrange a pilot, prospective customers typically contact Genohm for a tailored evaluation. Genohm's team can assist with a scoped proof-of-concept, provide sample configuration templates, and supply guidance on instrument connector setup and API usage. For details, review Genohm's services and contact information at https://www.genohm.com/.
No, Genohm is not generally free for production use. The company provides evaluation or limited trial access for pilot projects, but production usage is billed under Starter, Professional or Enterprise agreements depending on scale and feature needs. Small-scale proofs of concept may be available at reduced cost or as a time-limited trial, while production deployments require a paid subscription or contract.
Genohm exposes APIs to automate processes, integrate instruments and extract data for downstream analysis. The core API is RESTful and supports standard operations for creating and updating sample records, fetching run statuses, retrieving results and submitting pipeline jobs. Authentication is typically via OAuth2 tokens or SAML-backed SSO for enterprise customers, and the API includes pagination, filtering and field selection to support efficient data transfers.
Beyond CRUD-style endpoints, Genohm supports webhooks to notify external systems of status changes (for example, a completed sequencing run or a finalized report). That enables near-real-time automation where the LIMS notifies the pipeline orchestrator or an EMR system when a result is ready. For instrument-level automation, the platform provides adapters that can be extended or customized to parse proprietary output formats from major vendors.
The API surface also includes user and role management, audit log retrieval for compliance reporting, and endpoints for configuration objects so automation scripts can adapt to the same templates used in the UI. SDKs or example clients are commonly provided in Python and Java to help bioinformatics teams integrate Genohm into analysis workflows. For integration guidance and API documentation, see Genohm's developer and services materials at https://www.genohm.com/.
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Genohm is used for laboratory sample lifecycle management, workflow automation and data integration. It centralizes sample metadata, captures instrument outputs, orchestrates bioinformatics pipelines and produces auditable reports. Typical users include clinical sequencing centers, diagnostic labs and research organizations that require traceability and regulatory controls.
Yes, Genohm provides instrument connectors and adapters. The platform supports common sequencing platforms and laboratory devices via built-in adapters and configurable parsing rules. For custom instruments, customers can extend or request bespoke connectors during implementation.
Genohm pricing starts with pilot-level plans around $500/month and production tiers at approximately $2,000/month. Final costs are typically quoted per-site or per-deployment and depend on user counts, throughput, integrations and validation support. Enterprise pricing is provided by contract to reflect scoped services.
Yes, Genohm supports both on-premises and cloud deployments. Customers choose on-premises for data residency or low-latency instrument connectivity, while cloud deployments reduce infrastructure upkeep. Hybrid models are also common where sensitive data remains on-premises and other services run in cloud instances.
Genohm includes features to support regulatory compliance such as audit trails and electronic signatures. The platform provides the technical controls needed for ISO/GxP and GDPR workflows, but compliance also depends on implementation, validation and SOPs established by the customer. Genohm assists enterprise customers with validation planning and documentation.
Yes, Genohm offers a RESTful API and webhook capabilities for automation and integration. The API covers sample CRUD operations, run and result queries, user management and access to audit logs. SDKs or example clients in languages like Python are often provided to accelerate integration.
Yes, Genohm can integrate with EMR/ERP systems via standard interfaces and custom connectors. Integration methods include REST APIs, HL7/FHIR adapters where appropriate, and SFTP/file-based exchanges for legacy systems. These integrations are scoped as part of enterprise implementations.
Implementation timelines vary but small pilots can be live in weeks, while full production deployments typically take several months. Timeframes depend on workflow complexity, number of instrument integrations, validation requirements and data migration needs. Genohm's professional services can accelerate onboarding with templates and prebuilt connectors.
Yes, Genohm provides validation support and documentation for regulated deployments. The company assists with creating installation qualification (IQ), operational qualification (OQ) and performance qualification (PQ) artifacts and helps design validation test plans tied to configured workflows. Customers remain responsible for executing and maintaining validation activities after handover.
Genohm publishes integration and service information through its official site and support channels. For API references, deployment guides and integration best practices, consult Genohm's developer and services pages at https://www.genohm.com/ or contact their support team for access to the latest technical documentation.
Genohm hires across product, engineering, implementation and customer-facing roles focused on laboratory informatics. Positions commonly include software engineers with experience in data integration, bioinformatics engineers who understand sequencing workflows, product managers with domain knowledge in diagnostics and professional services consultants who lead deployments and validation projects. Career pages on the company website list open roles and provide details on required experience and application instructions.
Working at Genohm typically means engaging with regulated lab customers and complex integration challenges, so candidates should expect to work closely with clients on technical onboarding, instrument integrations and process optimization. Roles in customer success often require travel to customer sites for installation and validation support. The company also recruits for roles in QA, documentation and sales to support enterprise engagements.
For up-to-date job listings, candidate requirements and benefits, review Genohm's careers section and linked job postings at https://www.genohm.com/.
Genohm may operate reseller and implementation partner programs to expand delivery and integration capacity in different regions. Affiliates typically include system integrators, instrumentation vendors and specialized lab informatics consultancies that resell or implement Genohm solutions alongside complementary services such as validation, training and custom connector development. Affiliate programs allow customers to work with local partners for faster onboarding and localized support.
Partners are often certified through Genohm's partner program after training on the platform, which covers configuration best practices, connector development and validation workflows. Affiliates can be a practical option for organizations that prefer local project management while leveraging Genohm's core product and cloud services.
For information about partnership opportunities and authorized implementers, contact Genohm through their business development or partner pages at https://www.genohm.com/.
Independent reviews and customer feedback for Genohm are most often found in industry-specific forums, whitepapers and case studies published by genomics centers or diagnostic labs that have implemented the platform. Look for conference proceedings, application notes and vendor-neutral LIMS comparisons that include deployment experiences and ROI analysis. Peer-reviewed case studies from clinical or research organizations can provide insight into real-world performance and the challenges of instrument integration and validation.
Vendor-hosted case studies and reference customers are available on Genohm's website and should be read alongside independent sources for a balanced view. For hands-on evaluation, ask Genohm for references and pilot access to validate workflows and integration points in a controlled environment.
General software review aggregators and enterprise IT forums may contain user comments on usability, support responsiveness and implementation timelines, but you’ll often get the most relevant insights from direct conversations with similar labs and reference visits.