Dymension is revolutionary software that can analyse a typical 2D gel image rapidly. It features novel algorithms for background subtraction, noise filtering, precise warping, spot detection, rapid matching and reduced image editing time. Using its powerful spot detection algorithm, Dymension instantly locates and analyses protein spots. With Dymension, the entire analysis process from background correction to spot matching results and reporting takes minutes, making this the fastest 2D gel analysis package currently available.
Dymension is available in three versions, and upgrading between the packages is simple.
- Dymension 1. Dymension 1 is ideal for users looking for software to analyse spots between samples containing one 2D gel only. It offers a range of automatic image correction features and methods of resolving and analysing spots on single gels. The software can be easily upgraded to Dymension 2 or 3 if the proteomics needs of the laboratory change.
- Dymension 2. Dymension 2 has all the features of Dymension 1 but has the added ability to detect and compare protein spot maps in samples containing replicate gels. The software offers many background correction and noise filtering features including a SYPRO® Ruby filter, which can detect and automatically remove spots caused by SYPRO® Ruby crystals adhering to the gel, thus saving users valuable time editing their image. Dymension 2 is suitable for users that need to determine the amount of protein present before and after drug or protein induction treatments. The software automatically detects and assigns statistical confidence to each and every difference in spot normalised volume, thus accurately highlighting proteins of specific interest. The results of the analysis are displayed as a dynamically linked table, 3D spot profile, bar chart, correlation and scatter plot, which make it easy to compare many expression profiles simultaneously and therefore accurately pick proteins suitable for further analysis.
- Dymension 3. Dymension 3 is exciting software, which has all the functionality of Dymension 2 so can be used to analyse samples containing replicate gels. Dymension 3 has the additional capability to analyse multi-stained fluorescent gel images stained with up to three contrasting labels, eg, Cy™2, Cy™3 and Cy™5. This feature allows users to analyse multiple sets of any type of 2D protein gel, regardless of how it was stained, using only one software package.
Dymension 1 Features
| Feature |
Benefit |
| Icon driven user interface |
Simple software set-up and use |
| Accepts data from a TWAIN source |
Versatile as accepts gel images generated by most commercial scanners |
| Experiment set up wizard |
Fast, comprehensive analysis |
| Process flow chart |
Easy guide for user from image loading to obtaining results |
| Automatic background correction and noise filtering |
Saves time with spot editing |
| Automatic and precise sample warping |
Faster spot matching |
| Revolutionary spot detection algorithms |
Rapid spot detection and splitting |
| User definable spot detection parameters |
Flexible as allows user adjustments |
| Spot editing and filtering functions |
Control of spot editing and filtering parameters |
Dymension 1 Specifications
| Component |
Description |
| System |
Software for the rapid analysis of 2D protein spots between samples containing one gel only stained with visible or fluorescent dyes |
| On screen views |
Syncronised zoom with intensity autoscale |
| Image processing |
Automatic and precise image warping with vector view, background correction and noise filtering |
| Spot detection |
Automatic spot detection |
| Speed of spot detection |
3x10 Mbyte images in eight seconds |
| Spot matching |
Automatic spot matching |
| User definable parameters |
Spot detection with user adjustable parameters. Spot editing and filtering. Spot normalization |
| Image calibration |
pl and MW ladder calibration. Protein list assignment of spots with known identity, pl and MW |
| Power input |
Data visualisation |
Dymension 2 Features
| Feature |
Benefit |
| View results in a dynamically linked table, 3D spot profile, bar chart, scatter and correlation plot |
Easy to compare many expression profiles simultaneously and quickly select proteins of interest |
| Exports coordinates to automated spot pickers |
Fast and precise interface between Dymension and spot pickers |
| Automatic filtering of SYPRO® Ruby crystals |
Saves time with spot editing |
| Optional Gaussian spot fitting |
Choice of spot detection models |
| Automatic and precise replicate warping |
Faster spot matching as the replicate images are properly aligned |
| Automatic matching of samples containing unlimited number of replicates |
Improves accuracy by reducing manual editing time |
| Internet links to federated databases |
Quick presentation of protein sequence and structure |
| Dyversity compatible |
Direct analysis of GLP secure images using the Dyversity unique capture system |
Dymension 2 Specifications
| Component |
Description |
| System |
Software for the rapid analysis of 2D protein spots between samples containing replicate gels stained with visible or fluorescent dyes |
| On screen views |
Main pane and secondary panes for viewing replicates and samples. Syncronised zoom with intensity autoscale |
| Image processing |
Automatic and precise image warping with vector view. Manual warp editing. Automatic background subtraction and noise filtering. SYPRO® Ruby Crystal filter |
| Spot detection |
Automatic spot detection. Region of interest option. Gaussian spot modelling option |
| Speed of spot detection |
3x10 Mbyte images in eight seconds |
| Automatic spot matching |
Automatic warping and spot matching across multiple samples |
| User definable parameters |
Spot detection with user adjustable parameters. Spot editing, filtering and normalisation |
| Image calibration |
pl and MW ladder calibration. Protein list assignment of spots with known identity, pl and MW |
| Data visualisation |
Interactive process flow diagram. Histogram (brightness and contrast). Main pane and secondary panes for replicates and samples. Bar chart. 3D spot profile. Table of spot matching results. Scatter plot. Correlation plot. |
Dymension 3 Features
| Feature |
Benefit |
| View results in a dynamically linked table, 3D spot profile, bar chart, scatter and correlation plot |
Easy to compare many expression profiles simultaneously and quickly select proteins of interest |
| Exports coordinates to automated spot pickers |
Fast and precise interface between Dymension and spot pickers |
| Automatic filtering of SYPRO(R) Ruby crystals |
Saves time with spot editing |
| Optional Gaussian spot fitting |
Choice of spot detection models |
| Automatic and precise replicate warping |
Faster spot matching as the replicate images are properly aligned |
| Automatic matching of samples containing unlimited number of replicates |
Improves accuracy by reducing manual editing time |
| Analysis of multiplexed and non-multiplexed gels |
Cost effective as one software will analyse all types of 2D gel stains (eg Cy2, Cy3, Cy5), SYPRO® Ruby, Coomassie Blue) |
| Dyversity compatible |
Direct analysis of GLP secure images using the Dyversity unique capture system |
Dymension 3 Specifications
| Component |
Description |
| System |
Software for the rapid analysis of 2D protein spots between samples containing replicate gels, stained with visible or fluorescent dyes, and the analysis of multi-stained fluorescent gels |
| On screen views |
Main pane and secondary panes for viewing replicates and samples. Syncronised zoom with intensity autoscale |
| Image processing |
Automatic and precise image warping with vector view. Manual warp editing. Automatic background subtraction and noise filtering. SYPRO® Ruby Crystal filter |
| Spot detection |
Automatic spot detection. Region of interest option. Gaussian spot modelling option for non-multiplexed analysis |
| Speed of spot detection |
3x10 Mbyte images in eight seconds |
| Automatic spot matching |
Generates averaged gel image and performs average gel warping. Matches spots |
| Spot editing |
Spot detection with user adjustable parameters. Spot editing, filtering and normalisation |
| Image calibration |
pl and MW ladder calibration. Protein list assignment of spots with known identity, pl and MW |
| Data visualisation |
Interactive process flow diagram. Histogram (brightness and contrast). Main pane and secondary panes for multi-stained gel sets, replicates and samples. Bar chart. 3D spot profile. Table of spot matching results. Scatter plot. Correlation plot. |