- Open Access
GelJ – a tool for analyzing DNA fingerprint gel images
© Heras et al. 2015
- Received: 28 April 2015
- Accepted: 13 August 2015
- Published: 26 August 2015
DNA fingerprinting is a technique for comparing DNA patterns that has applications in a wide variety of contexts. Several commercial and freely-available tools can be used to analyze DNA fingerprint gel images; however, commercial tools are expensive and usually difficult to use; and, free tools support the basic functionality for DNA fingerprint analysis, but lack some instrumental features to obtain accurate results.
In this paper, we present GelJ, a feather-weight, user-friendly, platform-independent, open-source and free tool for analyzing DNA fingerprint gel images. Some of the outstanding features of GelJ are mechanisms for accurate lane- and band-detection, several options for computing migration models, a number of band- and curve-based similarity methods, different techniques for generating dendrograms, comparison of banding patterns from different experiments, and database support.
GelJ is an easy to use tool for analyzing DNA fingerprint gel images. It combines the best characteristics of both free and commercial tools: GelJ is light and simple to use (as free programs), but it also includes the necessary features to obtain precise results (as commercial programs). In addition, GelJ incorporates new functionality that is not supported by any other tool.
- DNA fingerprinting
- Image analysis
DNA fingerprinting is a technique for comparing DNA patterns that allows the analysis of the genomic relatedness among different samples, as well as to type and classify them. There are multiple DNA fingerprinting techniques, and the choice of which of them we must use depends on their applications (medical diagnosis, forensic science, parentage testing, food industry, agriculture, and many others) .
The interpretation of banding patterns by visual observation is a time-consuming and arduous task, especially when comparing distant, different and multiple patterns, and it can be highly dependent on the researcher. There are several commercial and freely-available software tools that can help to simplify this task and to eliminate the possible suggestibility derived of the human eye.
A survey of tools for analyzing DNA fingerprint gel images (from now on gel-images) was presented in . One of the conclusions of that survey was that commercial tools clearly overcome freely-available programs. In particular, free tools support the basic functionality for DNA fingerprint analysis, but they lack some instrumental features. For instance, free tools only supply a few options for increasing the quality of gel-images, work with straight lanes, only offer one or two methods for fingerprint comparison, cannot compare samples from different experiments and do not provide database support. The disadvantage of commercial tools is their price and complexity — in general, they are huge and complex tools with a considerable steep learning curve.
In this paper, we present GelJ, a feather-weight, user-friendly, open-source, platform-independent and free tool that overcomes the limitations of free programs and offers instrumental features for the proper analysis of gel-images.
GelJ has been developed as a Java application. It relies on 2 third-party Java libraries widely applied in bioinformatics: ImageJ  (that provides functionality for image processing) and Weka  (that features machine-learning algorithms including cluster analysis). Additionally, GelJ includes an embedded database provided by the JavaDB library .
There are three main concepts in GelJ: experiment, comparison, and study. An experiment corresponds to the analysis of a gel-image coming from a biological experiment. A comparison estimates the relatedness among samples from one or more experiments. Finally, a study gathers experiments and comparisons; in fact, experiments and comparisons always live on a study. These three concepts are integrated in the user-friendly graphical-user-interface of GelJ. This interface has been designed to smooth the learning curve, and it guides the user by means of metaphors, tooltips, wizards, and enabling/disabling functionality when needed.
The rest of this section is devoted to explain how experiments and comparisons can be created in GelJ using respectively the experiment wizard and the comparison wizard.
The experiment wizard
Step 1. Pre-processing. GelJ features several operations to increase the quality (but without altering the original data) of gel-images. First of all, the user can crop the image; subsequently, GelJ provides an option to invert the colors of the image (the user might prefer to work with dark- or light-background images); afterwards, the user can adjust (both manually and automatically) the brightness and contrast of the gel-image; and finally, GelJ offers other pre-processing operations that can be applied to the image. Namely, the additional operations are: flipping, rotating, filtering (GelJ includes the median, mean, minimum, maximum, variance, and Gaussian filters), background removal (applying the rolling ball mechanism ), and gamma correction. These additional operations include a preview option that allows the user to visualize the result before applying them. Some of the additional features (e.g. gamma correction or the application of filters) might be considered as “advanced”, but they can be ignored by a non-expert user without affecting the rest of the analysis — they have been included to improve the performance of further steps. The pre-processing functionality of GelJ is provided by the ImageJ library.
Step 2. Lane detection. GelJ automatically segments the lanes of a gel-image. The method implemented to perform this task is based on the following intuitive idea: since lane areas are covered with biological material, they appear lighter than the empty background areas between lanes; hence, strong intensity transitions between lanes and background are expected when moving horizontally across the image. This idea is captured using a vertical projection profile that averages the intensity values of each pixels column; and, subsequently, computing the local peaks of such a profile — a technique that has been successfully employed previously [7–9].
In some situations (e.g. if the quality of the image is low), the automatically-segmented lanes might need some adjustments — note that the precision of the lane-detection step influences the rest of the analysis. GelJ features several options to adjust the detected lanes. To be more concrete, it allows the addition and removal of lanes, and the adjustment of their thickness, position and curvature. Moreover, the user can adjust the brightness and contrast lane by lane, and also remove the background of individual lanes. Another feature provided by GelJ in this step is the possibility of including information (e.g. genus, species, or strain number) to each lane; such an information will be stored in the database for further use. Finally, in this step, the user must indicate the reference lanes that will be used for normalization.
Step 3. Normalization. GelJ normalizes gel-images to compare banding patterns within the same gel, and to compare patterns from different gels — this step is required since the band-positions of a lane are influenced by experimental conditions. Normalization among gels is achieved by introducing at least a reference lane that contains known DNA fingerprint patterns (reference markers). A reference marker consists of a set of band positions together with a physical property (mainly, the molecular weight) of each band of such a set. For example, in Pulsed Field Gel Electrophoresis (PFGE), these reference lanes can consist in commercial molecular markers (such as Lambda Ladder PFG Marker, Middle Range PFG Marker or Low Range PFG Marker) or reference strains (e.g. Salmonella enterica Braenderup H9812). In GelJ, the reference marker can be either loaded from a set of pre-defined markers or created from scratch — in the latter case, the marker is saved for further use.
The algorithm for normalization employed in GelJ follows the procedure implemented in . From the reference marker, the molecular weight of each band in the gel is computed. Briefly, this computation requires two interpolation stages. In the former, a vertical interpolation within a reference lane serves to derive a migration model — GelJ supports several migration models and it automatically picks a model that is suitable for most cases; additionally, the user can select a concrete model that is better adjusted to her reference marker. In the latter, a horizontal interpolation is performed to calculate the shift in each position of the non-reference lanes that fall between the reference lanes — this horizontal interpolation is automatically carried out using cubic-spline regression.
Some of the local peaks from the densitometric curves come from noise (see Fig. 3), and they are excluded by using a minimum height criterion: the value of a local peak must be higher than a fixed-minimum to be considered as the location of a band. The optimum height-threshold is not the same for all the gel-images, and the user of GelJ can manually fix this value. Additionally, the optimum height-threshold can also vary from region to region of the same gel-image; GelJ deals with this issue by means of a lane-threshold: the user can adjust the height-threshold for each lane of a gel-image. The different thresholds can be adjusted by means of sliders that are synchronized with the image (i.e. when the value of a slider is changed, the selected bands on the image are automatically changed and showed to the user).
In addition to the automatic detection of bands, the user can manually pick bands. Some uncertainties might arise during this process; in such a situation, the user can inspect the densitometric curve of the lane to decide about the inclusion of concrete bands — in GelJ, the densitometric curve is synchronized with the associated lane. GelJ also supports undo and redo functionality for manual band picking, this allows the user to easily undo actions carried our by mistake or go back to a previous state.
Once that the user has finished picking the bands of a gel, the molecular weights of the bands of each lane are automatically computed. Those weights are obtained taking into account the migration model and the shift of lanes that were previously computed in the normalization stage, this process is explained in . Finally, the list of molecular weights and the densitometric curve associated with each lane are stored for comparing such a lane with other lanes normalized with the same reference marker.
Finishing the experiment. Once the user has finished the analysis of an image (i.e. the four above steps have been completed), a new experiment is stored in the GelJ database and added to the main panel of the GelJ interface (see Fig. 1). Such an experiment will contain information like name, date or the image that was used to create the experiment; and, it will have associated a number of lanes, that correspond to the lanes of the analyzed image. By default, the user can add some fixed information (e.g. genus, species, strain number or country) to each lane; additionally, the user can also create on-the-fly new information fields (e.g. age or laboratory) to be added to the lanes of the experiment.
The comparison wizard
The main goal of DNA fingerprinting is the comparison of samples through the inspection of band patterns. This is usually a three-step process: selection of lanes to compare, computation of similarity matrices, and construction of dendrograms (a tree representing the relatedness among lanes ). GelJ provides a wizard that guides the user in the comparison of lanes by configuring several parameters related to compared lanes, similarity matrices, dendrograms, and the final output.
Lanes. The user can either automatically add all the lanes or choose manually some lanes from the experiments of her current study to be included in the comparison — provided that the experiments have been normalized using the same reference maker. As we have explained previously, the user can create experiments using the experiment wizard, but also import experiments from her studies or studies belonging to other users.
Similarity matrices. Given a list of n lanes, L, the similarity matrix of L is an n×n matrix where the element of row i and column j encodes the similarity between the i-th and j-th lanes of L. There are two approaches to calculate the similarity between lanes: band-based and curve-based .
In the curve-based approach, the similarity is determined using a correlation coefficient computed from the densitometric curves of the lanes. GelJ supplies several curve-based methods for computing the similarity among lanes: Pearson correlation, Cosine coefficient, Euclidean distance, and Manhattan distance.
Currently, there is no consensus on which measure provides more accurate results , and all the metrics implemented in GelJ have been widely employed in the literature (being the Dice coefficient the most used band-based measure, and the Pearson correlation the most used curve-based measure ). GelJ automatically selects Dice as similarity measure, and the by-default tolerance parameter provided by GelJ is good enough in most of the cases. Moreover, GelJ allows the user to choose a different similarity measure and change the tolerance value — those changes will be remembered for further use.
A more detailed explanation of the band-based and curve-based measures included in GelJ, together with a visual comparison of them, is provided in the supplementary materials.
Dendrogram generation. Using the similarity-matrices, GelJ uses the clustering algorithms implemented in Weka  to generate dendrograms. The construction of dendrograms follows an iterative process: at each step, the nearest two clusters (sets of fingerprints) are combined into a higher-level cluster. The difference among the methods relies on how the distance between the new clusters is recomputed. GelJ offers different methods to construct dendrograms based on hierarchical clustering : UPGMA, UPGMC, single linkage, complete linkage, mean linkage, and Ward. GelJ automatically selects UPGMA (the most used method ), but it also allows the user to employ a different method, that will be remembered for future use – a detailed explanation of the clustering methods included in GelJ is provided in Additional file 2.
Output. The main output generated by the comparison wizard is a dendrogram showing the relations among the compared lanes (see Fig. 1). The dendrogram generated by GelJ might include additional information associated with each lane included in the comparison — both graphical (lane images, band position and a combination of lanes and bands) and textual information (data previously stored in the database). The usefulness of adding this extra information to dendrograms is threefold: firstly, graphical information helps to check whether the results depicted in the dendrograms are consistent; secondly, textual information identifies lanes from the same or multiple experiments; and finally, since dendrograms can be saved as images, the user can introduce information in them without using an external program. In addition to the dendrogram, GelJ can also generate the similarity matrix associated with a comparison: this similarity matrix can be used to inspect the concrete relation (a numerical value) between two lanes. Finally, the comparison is stored in the GelJ database to be inspected or modified later on.
GelJ has been successfully tested on a battery of 65 images taken from agarose pulsed-field gel electrophoresis (PFGE)-gels — GelJ can also be applied without any special hindrance to gel-images obtained using other techniques such as RAPD, rep-PCR, AFLP, SSR and so on. In each gel of our dataset, at least two lanes were placed with molecular weight reference markers (Lambda Ladder PFG Marker, Middle Range PFG Marker or Low Range PFG Marker) and the plugs of the test samples were placed in the remaining lanes. The conditions were different according to the enzyme and bacteria used.
Gels were visualized with ultraviolet light and were photographed with Image Store 5000 UVP thanks to the software ChemiGenius (GenSnap from SynGene).
In the rest of this section, we provide a comparison of the features included in GelJ with the functionality supported by the most-complete tools employed to analyze gel-images. A survey of this kind of tool was presented in . From the 33 tools studied in that survey, 15 of them provide the 5 stages to compare samples from gel-images (i.e. pre-processing, lane segmentation, normalization, band detection, and fingerprint comparison); in turn, among the 15 tools, there were 5 commercial tools (GelComparII , GelQuant Pro , ImageQuant , Phoretix 1D-Pro , and TotalLab ) that excelled the rest of them. We contrast GelJ with these 5 commercial programs and also with the 2 best free tools (GelClust  and PyElph ).
GelJ exceeds the features available in free tools and provides similar functionalities, regarding the analysis of gel-images, to commercial tools in the 5 stages to compare samples from gel-images. Namely, considering the different steps, we have the following comparison (the complete list of features supplied by GelJ and a detailed comparison with the other tools are provided in the Additional file 3: Tables 1–7 for the former and Additional file 4: Tables 8–17 for the latter).
Pre-processing. GelJ supports several image operations for increasing the quality of gel-images, exceeding the functionality included in the other tools. To be more concrete, the free tools only implement basic operations (e.g. PyElph implements cropping, rotating, and filtering), and commercial tools lack some functionality implemented in GelJ (e.g. GelComparII does not implement gamma correction, or the user of GelQuant Pro cannot invert the colors of the image using such a program).
Lane detection. The functionality related to this stage illustrates that free tools lack some instrumental features to obtain accurate results. All the compared tools can automatically detect the lanes of gel-images, and the user can manually add and remove lanes. However, the users of free tools cannot obtain curved lanes, define lanes with different thickness (this feature is available in GelClust but not in PyElph) or subtract the background of a given lane (feature supported by PyElph but not by GelClust); on the contrary, commercial tools offer those features. GelJ supports all the options for lane-detection available in the commercial tools; moreover, the user can adjust (both manually and automatically) the brightness and contrast of individual lanes — an important issue when the quality of the different regions of a gel-image varies.
Normalization. The differences among the programs in the normalization step rely on two aspects: whether the reference markers can be saved and loaded, and the number of migration models offered by the tools. In the former aspect, GelClust is the only tool that does not save reference markers for further use. In the latter aspect, GelJ offers the same migration models than the commercial tools (including, 1st – 3rd degree curves, cubic splines, logarithmic and so on), and also some additional ones (e.g. Gaussian or Rodbard).
Band detection. In this step, all the programs provide similar functionality (automatic band detection, height threshold, manual picking, and densitometric-curve display). Moreover, GelJ and the commercial tools provide additional features that simplify the band-detection task: synchronization of the histogram with the gel-image (bands can be added from the histogram), and undo/redo functionality for picking bands. GelJ is the only tool that offers the lane-by-lane threshold functionality to detect bands automatically.
Fingerprint comparison. In this stage, tools can be configured using four parameters: (P.1) lanes to compare, (P.2) similarity method, (P.3) clustering method, and (P.4) output. For Parameter P.1, GelJ, GelComparII, and Phoretix 1D Pro are the only tools that can compare lanes from different gel-images (note that this feature requires database support). For Parameter P.2, GelJ implements all the band- and curve-based similarity-methods available in the other tools (and also some methods, for instance the Euclidean distance, that are not implemented in any other program). For Parameter P.3, the only clustering method that is not implemented in GelJ, but is available in other tools, is neighbour joining; however, GelJ implements the UPGMC and mean linkage methods that are not supported by the rest of the tools. Finally, for Parameter P.4, the user can select the same options in GelJ than in GelComparII for dendrogram output — the most complete program regarding this parameter. In addition, given a lane, GelJ can find lanes that are similar to such a lane — this feature is only supported by GelJ and GelComparII.
General features. Apart from the specific features for the analysis of gel-images, it is worth mentioning some of the general characteristics of GelJ. This tool is free, open-source, platform-independent, light (∼ 15 MB) and does not require installation — the only requirement to run GelJ is Java (available in most computers). In the development of GelJ, a special emphasis has been put on creating a user-friendly interface that guides the user by means of metaphors, tooltips, wizards, enabling/disabling functionality when needed, automatically picking the most common methods employed in the literature (e.g. Dice for similarity measure and UPGMA for clustering), automatically selecting values that work properly in most situations (e.g. the tolerance value or the migration model), and remembering selected parameters when these are changed. Moreover, GelJ provides several database features; for instance, exporting/importing experiments (this functionality allows users to share their experiments and compare their fingerprints with the ones from other users) and the creation of backups.
In this paper, we have presented GelJ, a Java application designed for analysing DNA fingerprint gel images. GelJ is a user-friendly, platform-independent, open-source, and free tool that combines the simple design of free programs with instrumental features for the analysis of gel-images that are only available on commercial tools (e.g. mechanisms for accurate lane-detection, band- and curve-based methods for computing similarity among lanes, tools for searching similar samples across gels, or database support). Besides, it includes new features that are not avail in any other tool; for instance, lane-by-lane threshold for band detection or the adjustment of brightness and contrast for individual lanes.
As a further work, it remains the task of increasing the automation of GelJ. For instance, the global and lane-by-lane thresholds for band detection are values that must be fixed by the user; hence, it would be interesting to create an expert system that could automatically select these values by learning from the user’s experience.
Project name: GelJ.
Project home page: https://sourceforge.net/projects/gelj/.
Operating system(s): Platform independent.
Programming language: Java.
Other requirements: Java 6 or higher.
License: GNU GPL v3.
Any restrictions to use by non-academics: restrictions specified by GNU GPL v3.
GelJ does not require installation. To run GelJ, the user should download GelJ from the project home page, unzip the downloaded file, and run the program geljv1_*.jar. The only requirement to run GelJ is the installation of Java; the user can check whether Java is installed in her computer using the following link: https://www.java.com/en/download/installed.jsp?detect=jre.
Several videos explaining how to use GelJ are provided as Additional files 5-12. Additional file 13 supplies several images to test GelJ. All these materials are also available in the Wiki page of the project home page.
This work was partially supported by the Agencia de Desarrollo Económico de La Rioja (ADER) [2013-I-IDD-00123] and Ministerio de Economía y Competitividad [MTM2014-54151-P].
Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
- (Read MM, editor.)2005. Trends in DNA Fingerprint Research. New York, USA: Nova Science Publishers, Inc.Google Scholar
- Heras J, Domínguez C, Mata E, Pascual V, Lozano C, Torres C, et al. A Survey of Tools for Analysing DNA Fingerprints. Brief Bioinform. 2015. doi:10.1093/bib/bbv016.
- Schneider CA, Rasband WS, Eliceiri KW. NIH Image to ImageJ. Nat Methods. 2012; 9:671–5.View ArticlePubMedGoogle Scholar
- Hall M, Frank E, Holmes G, Pfahringer B, Reutemann P, Witten I. The weka data mining software: An update. SIGKDD Explorations. 2009; 11(1):10–18.View ArticleGoogle Scholar
- Oracle. JavaDB Reference Manual. Technical report. 2014. http://www.oracle.com/technetwork/java/javadb/overview/index.html.
- Sternberg SR. Biomedical Image Processing. Computer. 1983; 16(1):22–34.View ArticleGoogle Scholar
- Vauterin L, Vauterin P. Integrated Databasing and Analysis In: Stackebrandt E, editor. Molecular Identification, Systematics, and Population Structure of Prokaryotes. Germany: Springer: 2006.Google Scholar
- Ismail I, Eltaweel GS, Nassar H. Bands detection and Lanes segmentation in DNA Fingerprint images. J Inf Comput Sci. 2014; 9(4):243–51.Google Scholar
- Skutkova H, Vitek M, Krizkova S, Provazník I. Preprocessing and Classification of Electrophoresis Gel Images Using Dynamic Time Warping. Int J Electrochemical Sci. 2013; 8:1609–1622.Google Scholar
- Anderberg MR. Cluster Analysis for Applications. New York, USA: Academic Press; 1973.Google Scholar
- Hassan WM, Wang SY, Ellender RD. Methods To Increase Fidelity of Repetitive Extragenic Palindromic PCR Fingerprint-Based Bacterial Source Tracking Efforts. Appl Environ Microbiol. 2005; 71(1):512–8.View ArticlePubMedPubMed CentralGoogle Scholar
- Applied Maths NV. GelCompar II version 6.6.11. 2013. http://www.applied-maths.com.
- DNR Bio-Imaging Systems Ltd. GelQuant Pro version 13. 2013. http://www.dnr-is.com/Product.asp?Par=3.19&id=81.
- GE Healthcare Life Sciences. ImageQuant TL 7.0. 2010. http://www.gelifesciences.com/.
- TotalLab Limited. Phoretix 1D Pro version 11.4. 2013. http://totallab.com/cliqs-1d-pro/.
- TotalLab Limited. TotalLab Quant version 13. 2013. http://totallab.com/cliqs/.
- Khakabimamaghani S, Najafi A, Ranjbar R, Raam M. GelClust: A software tool for gel electrophoresis images analysis and dendrogram generation. Comput Methods Programs Biomed. 2013; 111(2):512–8.View ArticlePubMedGoogle Scholar
- Pavel A, Vasile C. PyElph – a software tool for gel images analysis and phylogenetics. BMC Bioinform. 2012;13(9). doi:10.1186/1471-2105-13-9.