Molecular Dx

Reduce manual steps from molecular test intake to authorized reporting.

Build your molecular testing Digital Brain with Scispot. Automate data capture, instrument imports, and review routing so complete specimen records reach qualified staff for clinical review and authorized reporting.
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Explore LabOS

Trusted by 200+ life science labs

Supporting 250+ instrument types, more than 1,000 experiments each month, and millions of samples across diagnostics, genomics, biotech, and regulated testing.

Your best fit

Built for molecular teams managing growing volume and manual handoffs.

Connect PCR-based assays, extraction, and controlled result review in clinical and reference labs. Start where staff repeatedly check status, copy instrument values, or chase repeat requests.

Map your molecular workflow
Features

Published Customer Outcomes

Reported results from individual molecular testing workflows.

70%

Fewer data-entry errors

One Canadian molecular diagnostics customer; transcription and duplicate-entry errors.

60%

Fewer update delays

A Cambridge molecular diagnostics lab connected tracking, notifications, and instrument data.

45%

Faster sample processing

The Cambridge lab connected specimen records, instrument data, and workflow checks.

≈8 h/week

Staff time recovered

Cambridge lab staff recovered time through routine automation.

One system, three layers

A Digital Brain from specimen data to the right review queue.

Route orders into preparation

Capture orders, specimen barcodes, collection details, and receipt assessments once. Check required fields and route missing information or acceptance exceptions to responsible staff.

Keep tests and method versions with each specimen. Bench teams see what can proceed and what needs clarification, rejection, or a recorded recollection decision.

Capture run data and controls

Carry identities through extraction, aliquots, plates, and runs. GLUE maps supported instrument outputs to assay records, retaining original files, reagent lots, operators, and method versions.

Run configured completeness and control checks. Route exceptions with affected specimens so qualified reviewers can assess the evidence and determine the next step.

Prepare results for authorized reporting

Assemble results, controls, repeats, and required records for review. Prepare configured report fields and expose missing evidence; draft reports remain distinct from issued versions.

Authorized staff decide whether to report, withhold, or request more work. Preserve approved versions, source relationships, and earlier reports with each amendment’s reason.

One connected operating layer

Testing should move forward without repeated status calls.

Scispot moves required specimen data and tasks between orders, extraction worksheets, instrument files, and reports. Unresolved controls and missing records stay visible before authorization.

Ask which specimens need attention
before the next review.

Find missing work and prepare a clear handoff.

Meet Scibot
Scibot, the Scispot AI coworker
Which specimens are waiting for extraction?
Show runs with unresolved control exceptions
Find reports missing required review records
Trace this result to its instrument file
Summarize repeats for specimen MDX-S041
Draft a handoff for the review queue
Which specimens are waiting for extraction?
Show runs with unresolved control exceptions
Find reports missing required review records
Trace this result to its instrument file
Summarize repeats for specimen MDX-S041
Draft a handoff for the review queue
AI-native lab transformation

Less manual handling from accessioning through result review.

Ready Work for Each Bench

Prepare accessioning, extraction, and repeat-testing queues from shared specimen records. Required-field checks expose missing information before staff start the next step.

Instrument Imports With Clear Exceptions

GLUE maps supported outputs to specimens, assays, and controls. Preserve source files and route incomplete or conflicting records to the responsible reviewer.

Prepared Records for Authorized Review

Bring controls, repeat history, and report fields into review. Configure sign-offs and output templates around approved procedures so staff assess evidence before authorization.

Personalized Tasks With Expert Delivery

Jazz gives preparation staff and reviewers focused screens on shared Scispot data. Our scientists and engineers configure workflows, test normal and exception cases, and train teams.

Automate the handoffs that slow molecular testing.

01

PCR Testing From Intake to Report

Reduce copying from receipt through report preparation.

Route accepted specimens into extraction and assay queues. Import supported outputs using agreed specimen and plate mappings; run configured checks while retaining controls and original files.

Prepare results and report fields for authorized review. Missing records and control exceptions remain linked to affected tests. Qualified staff decide whether a result can be issued.

Explore PCR testing workflows

02

Repeat Testing With Full History

Route approved repeats to the team performing them.

Record each repeat’s reason and scope, then assign the preparation or assay work. Reuse specimen identity and applicable method context while preserving the original run.

Bring both runs and review decisions into the case. Reviewers determine final disposition; amended outputs retain the earlier version and recorded reason for change.

Explore repeat-testing workflows

03

Multi-Assay Molecular Lab Operations

Give each team a queue built on shared specimen records.

Configure preparation, control-review, and authorization queues. Jazz presents each role’s fields and tasks on shared Scispot data, keeping method versions and review states distinct across assays.

Our scientists and engineers map LIS and instrument handoffs, test exceptions, and train users. Start with one assay; measure manual handling or review readiness before expanding.

Explore molecular lab work queues

Choose the molecular test with the most manual handoffs.

Bring a test workflow, instrument output, and report example. Our scientists and engineers will scope and test a handoff, measuring manual handling or review readiness with laboratory approval control.
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FAIR data • pipelines • automation

Instruments • ELN/LIMS/SDMS • 200+ connectors

FAIR data • pipelines • automation

Instruments • ELN/LIMS/SDMS • 200+ connectors

Frequently asked questions

Is this solution for a testing laboratory or a diagnostic kit company?

This solution serves laboratories receiving specimens, performing molecular tests, reviewing controls and results, and issuing authorized reports. Diagnostics & Kits covers assay development, product versions, kit lots, and validation evidence. Scispot automates digital work around your procedures and can connect both workflows when a company develops products and operates a testing lab.

Which molecular instruments and clinical systems can Scispot connect?

Connections depend on available interfaces and outputs, including extraction platforms, qPCR instruments, sequencers, and preparation tools. We review representative files or messages, identifiers, security, and exchange direction. The agreed scope defines import matching, missing-field handling, and which system owns the authorized report.

Can we introduce Scispot without replacing our existing LIS?

Keep your LIS and begin with one handoff, such as instrument import to control review. Our scientists and engineers map record ownership, configure connections and task screens, test normal cases, exceptions, and reconciliation, then support training and rollout within scope. Measure manual handling and use before expanding.

How are assay controls, reruns, and amended reports handled?

Configured workflows retain controls, route exceptions, and link original tests to repeats with reasons and dispositions. Report preparation uses selected records; authorization stays separate. Your laboratory defines assay rules and interpretation: an isolated Cq value does not determine a clinical result. Amendments preserve earlier outputs and change reasons.

How does Scispot support quality requirements in a molecular laboratory?

Scispot supports permissions, audit history, electronic signatures, review steps, and source-linked records. Trust Vault organizes controlled evidence. Your laboratory defines intended use, required validation, procedures, and regulatory obligations. Qualified staff retain clinical interpretation, assay acceptance, and report authorization; requirements depend on location, test menu, and quality system.

Support controlled testing and authorized reporting.

Scispot supports record controls, audit history, source traceability, and review steps. Your laboratory owns validation, quality procedures, clinical interpretation, regulatory obligations, and report authorization.