
Offline Flow Cytometry Data Analysis Software
离线流式细胞术数据分析软件
- ISO 9001 software development (to be confirmed)
- +2
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流式细胞仪采集与控制软件
Price on request — FOB / CIF quoted per order
Prices depend on configuration, quantity and destination port.
| Operating system | Windows 10/11 (64-bit) |
|---|---|
| Output format | FCS 3.1 |
| Instrument coupling | Model-specific |
| Maximum parameters | Up to 60+ (model dependent) |
| Maximum acquisition rate supported | Up to 100,000 events/s (instrument limited) |
| QC module | Bead-based with Levey-Jennings tracking |
By Lab Manufacturers China Technical TeamLast reviewed Standards: ISAC FCS 3.1 data standard, ISAC FCS 3.2 data standard, ISAC MIFlowCyt
Flow cytometer acquisition and control software operates the instrument, sets detector voltages and thresholds, runs quality control and writes list-mode FCS files during data collection. It is tied to a specific cytometer model and is the first software layer needed on any new instrument workstation.
Flow cytometer acquisition and control software operates the instrument, sets detector voltages and thresholds, runs quality control and writes list-mode FCS files during data collection. It is tied to a specific cytometer model and is the first software layer needed on any new instrument workstation.
Acquisition software provides the operator interface for startup, fluidics control, laser and detector configuration, and data recording. Users define experiment templates with parameter lists, voltage or gain settings, thresholds, stop conditions and plot layouts. Daily quality control modules run calibration beads and track performance in Levey-Jennings charts, flagging deviations in sensitivity, CV or laser delay. During acquisition, real-time plots and gating support setting sort gates and verifying compensation, and an automated compensation setup uses single-stain controls to calculate matrices. Data are stored in FCS 3.1 files with experiment metadata, and export tools transfer them to network storage. User accounts with permission levels restrict who can change instrument settings. The software runs on a validated Windows workstation supplied with the instrument, and firmware and software updates must match the hardware.
Cytometry software handles three stages. During acquisition it configures detector voltages, thresholds and gains, triggers on defined parameters, and writes each event's scatter and fluorescence values to list-mode FCS files with metadata. Analysis software then applies compensation or spectral unmixing to correct spillover, transforms data with logicle or biexponential scales to display negative values, and lets users draw hierarchical gates on histograms and dot plots to define populations. It calculates statistics such as percent parent, median fluorescence intensity and coefficient of variation. High-dimensional tools add dimensionality reduction with tSNE or UMAP and unsupervised clustering with algorithms such as FlowSOM or PhenoGraph. Regulated platforms add user authentication, audit trails, electronic signatures and validated templates.
A typical flow cytometer acquisition and control software configuration offers operating system of Windows 10/11 (64-bit), output format of FCS 3.1, instrument coupling of Model-specific, maximum parameters of Up to 60+ (model dependent), maximum acquisition rate supported of Up to 100,000 events/s (instrument limited) and QC module of Bead-based with Levey-Jennings tracking. Values are indicative of the product class; the exact figures for each configuration are confirmed on the quotation and the calibration documents supplied with the instrument.
The Flow Cytometer Acquisition and Control Software is used in daily instrument startup and QC, panel acquisition with templates, cell sorting control, plate and tube loader runs and multi-user core facility operation. Across the wider Cytometry Software class, laboratories also deploy it for instrument acquisition and quality control, offline flow data analysis and reporting and high-dimensional immune profiling.
Relevant standards and methods include ISAC FCS 3.1 data standard, ISAC FCS 3.2 data standard, ISAC MIFlowCyt, 21 CFR Part 11, EU GMP Annex 11, GAMP 5 and CLSI H62. Certification candidates for this model are ISO 13485 software lifecycle, IEC 62304 software process and CE; each is to be confirmed for the specific configuration before shipment, and certificates are supplied only where they have been issued.
Install acquisition software only on the validated workstation supplied or approved for the cytometer, with operating system updates under change control. Back up FCS data to network storage on a schedule and follow the MIFlowCyt guideline to record experiment metadata for reproducibility. Validate compensation matrices with single-stain controls and review gating strategies with fluorescence-minus-one controls. Standardize gating templates across users to reduce analyst variability. For regulated work, perform installation, operational and performance qualification, lock methods and templates, and review audit trails periodically. Keep license keys and software versions documented, and confirm that exported data remain readable in future software releases.
Acquisition software is chosen with the cytometer, not independently, so confirm the version, licensing and upgrade path for your model. Request validation documentation if the lab is regulated. In an RFQ specify operating system, user management, QC features, loader support, data export formats and support terms.
Select software according to the task and the regulatory environment. Confirm instrument compatibility first, since acquisition software is tied to a specific cytometer and firmware. For analysis, verify support for FCS 2.0, 3.0, 3.1 and 3.2 files, compensation and unmixing matrices, batch processing and export of publication-quality graphs. For high-dimensional work, check for built-in tSNE, UMAP, FlowSOM and integration with R or Python. Regulated laboratories need 21 CFR Part 11 or equivalent functionality, meaning audit trails, electronic signatures, role-based access and validation documentation. Consider licensing model, including perpetual, subscription, floating or site licenses, data storage and cloud options, operating system support, and whether technical support and training are available locally.
| Operating system | Windows 10/11 (64-bit) |
|---|---|
| Output format | FCS 3.1 |
| Instrument coupling | Model-specific |
| Maximum parameters | Up to 60+ (model dependent) |
| Maximum acquisition rate supported | Up to 100,000 events/s (instrument limited) |
| QC module | Bead-based with Levey-Jennings tracking |
| Compensation | Automated and manual matrix |
| User management | Role-based accounts and passwords |
| Data export | FCS, CSV, PDF reports |
| Workstation RAM | 16 GB or more |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Generally no. It must run on the validated workstation and operating system specified for the cytometer, because it communicates with instrument electronics through dedicated interfaces. Unapproved hardware or updates can cause communication errors and invalidate support.
It is a software function that runs fluorescent calibration beads, measures laser alignment, detector sensitivity and CV, and records results over time. Levey-Jennings charts show drift so operators can correct issues before acquiring experimental samples.
Most modern packages calculate a compensation matrix automatically from single-stain controls, either cells or beads, and apply it during acquisition or store it with the file. Users should still review the matrix visually and verify with multicolor controls.
It controls the instrument during acquisition, records each event to FCS files, and then supports analysis by compensation, gating, statistics and plotting. Advanced software adds dimensionality reduction, clustering and batch processing, and regulated packages add audit trails and electronic signatures.
FCS is the Flow Cytometry Standard defined by the International Society for Advancement of Cytometry. It stores list-mode event data and metadata such as parameters, voltages and compensation in a single file, with versions 3.0, 3.1 and 3.2 in current use.
You need it when electronic records support regulated decisions, such as GMP release testing or clinical trial submissions to the FDA. Compliance requires audit trails, electronic signatures, access control and validation, and the lab's procedures must also support these controls.

离线流式细胞术数据分析软件

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