Designed primers are stored on the web server for a limited period, allowing users to design multiple primer pairs and combine them in a single order. Users, or actually web clients, are identified using cookies that expire after a set period currently one week. Primers can also be saved locally as a FASTA file and previously saved primers can be uploaded allowing the addition of new primers to an existing primer collection.
In case Primer3Plus is run on a local server, the order form can be customized allowing tight integration into a laboratory primer order management system. We discriminate five distinct primer design user scenarios, or tasks, that have been integrated in the new interface.
These tasks can be selected using a drop down list at the top of the Primer3Plus page. More tasks might be added in future versions of the Primer3Plus web interface. The Detection task can be used for designing standard PCR primers or hybridization oligos to detect a given sequence.
The user provides the template sequence and optionally indicates target regions within the sequence or changes the parameters for primer picking. By pressing the Pick Primers button a list of suggested primer pairs is presented, ordered with the best pair at the top. The Detection task is most reminiscent to the original Primer3 web interface.
For cloning a PCR product in a specific reading frame in an expression vector, it is important to control precisely the start and end of the PCR product. The output lists the predicted best fitting primer pairs that start or end at the given position.
Subsequently, the user can modify the primer sequence, e. Fixing primer ends significantly limits the number of possible candidates that fulfil the stringent default settings.
If this is the case, alternative primers are given that are accompanied by a warning concerning the relaxed stringencies that have been applied Figure 2. Result page of a Primer3Plus Cloning run showing the left and right primers in blue and yellow.
The included region is colored green. Alternative primer pairs of lower quality are shown below the sequence truncated here. The Sequencing task is developed to design a series of primers on both the forward and reverse strands that can be used for custom primer-based re- sequencing of clones. The spacing of primers is configurable within the Advanced settings tab, as is the overlap between the forward and reverse primers. A configurable number of nucleotides immediately following the primer that usually cannot be read reliably, are taken into account when selecting the forward and reverse primers.
The Primer Check task can be used to obtain information on a specified primer, like its melting temperature or self complementarity. This can, for instance, be useful when certain primers are to be reused under different experimental conditions or if the original primer characteristics were lost. The Primer Check option is also available on the Primer3Manager page, enabling a re-check of primers that have been modified by the user, e.
When this task is selected, no template sequence is required and only the primer sequence has to be provided. With the Primer List task, all possible primers that can be designed on the target sequence and meet the current settings will be returned with their corresponding characteristics.
This task basically allows manual selection of primers, which could be of interest in case of specific tasks that are not yet implemented in Primer3Plus like picking overlapping primers. The run time of the Primer List task can be relatively long when compared to the other Task options, and can take up to a minute, especially when lengthy target sequences are submitted. The JavaScript is not essential for proper function of Primer3Plus and can be disabled.
The Primer3Plus web interface has been tested to run properly on the most recent versions of Firefox, Internet Explorer, Safari and Konqueror. The server side software has been written in Perl, using the CGI standard for communicating with the Apache web server. Please consider releasing your software under GPL3 as well, especially if you do not want to maintain it in the future.
There is no need to ask us for permission to include primer3 in your tools. Lander , but ongoing development and maintenance are not currently funded. Primer3 was originally written by Helen J. The original web interface was designed by Richard Resnick. In addition, among others, Ernst Molitor, Carl Foeller, and James Bonfield contributed to the early design of primer3.
Brant Faircloth has helped with ensuring that primer3 runs on Windows and MacOS and with the primer3 web site. This makes the interface powerful, but at the same time confusing for occasional users. Primer3Plus provides an intuitive user interface using present-day web technologies and has been developed in close collaboration with molecular biologists and technicians regularly designing primers.
It focuses on the task at hand, and hides detailed settings from the user until these are needed. We also added functionality to automate specific tasks like designing primers for cloning or step-wise sequencing.
Settings and designed primer sequences can be stored locally for later use. Finally, primers selected by Primer3Plus can be sent to an order form, allowing tight integration into laboratory ordering systems. Moreover, the open architecture of Primer3Plus allows easy expansion or integration of external software packages. Oligonucleotide primers are widely used in various molecular biology techniques like DNA sequencing and the polymerase chain reaction PCR.
Since a primer serves as the starting point for DNA replication, specific binding of the oligonucleotide to the target sequence on the template strand is essential for a successful experiment. The binding specificity of a primer is determined by several of its properties, like the melting temperature Tm , GC-content and self complementarity. Designing primers is usually done with the help of computer programs, among which Primer3 is most widely used judging from the hundreds of citations of the primary publication 1.
Primer3 is popular since the program can be used online and is redistributed free of charge. Recently, a SourceForge project was started for Primer3 in which several improvements are being discussed and implemented. Subsequently Primer3 was updated to include an additional method for Tm calculation [SantaLucia model, 2 ], since it was argued that primer design based on the Breslauer model shows variation in the predicted Tm 3 , 4.
The web interface is one large form showing all possible options. This makes it powerful, but at the same time confusing for the occasional user; without in-depth knowledge it is hard to tell which of the settings are important for a specific design task.
Some tasks, like designing PCR primers for position specific cloning, are not easy to perform with the current web interface, since this would require multiple runs of the program under different settings. We aimed to design the Primer3Plus web interface in such a way that it is comprehensible for occasional users, and yet powerful for the experienced users that need to do more complex or laborious tasks.
Where the original Primer3 web interface presents all options and settings in one large web page, Primer3Plus starts with a more simple screen containing only the input boxes for the sequence and the option to select the target region for amplification Figure 1. Also a new task selection box is included top left corner , that provides the possibility to select between five different scenarios for which Primer3Plus can be used see subsequently.
Screenshot of the Primer3Plus start page. In contrast to the original Primer3 web interface, detailed settings that are not frequently used are hidden behind tabbed panels. A pull-down task menu is added top left that provides five scenarios for which Primer3Plus can be used: gene detection, primers for cloning purposes, sequencing, list of all possible primers and check option for already available primers.
Here an example sequence GFP was loaded, the Cloning task selected and the open reading frame marked as included region. For most purposes the default parameter settings are adequate.
Adjusting these parameters is possible by using the tabbed panels. The tabs are ordered in the most likely frequency of use, with the left most panel being the start page, followed by the general settings, advanced settings, internal oligo options, penalty weights and sequence quality. The parameter names were kept the same as in the original Primer3 interface to minimize time needed to get familiar with using Primer3Plus.
The labels of the parameters are web links to a context-sensitive help text, just like in the original Primer3 web interface. Primer3Plus adds to this a floating tool tip with a brief description for some of the most prominent parameters. Next to the default settings, the user can choose specific settings for special tasks like primer design for qPCR applications.
It is also possible to store custom settings locally to save the user from having to go through the configuration each time primers are designed for specific non-standard conditions, like AT-rich organisms or high-salt environments. The Primer3Plus results page shows the suggested primers with their characteristics, ordered from best to worst. The best scoring primer pair is marked on the template sequence.
The selected primers can be submitted to the Primer3Manager where the user can manage a primer collection. Designed primers are stored on the web server for a limited period, allowing users to design multiple primer pairs and combine them in a single order.
Users, or actually web clients, are identified using cookies that expire after a set period currently one week. Primers can also be saved locally as a FASTA file and previously saved primers can be uploaded allowing the addition of new primers to an existing primer collection.
In case Primer3Plus is run on a local server, the order form can be customized allowing tight integration into a laboratory primer order management system. We discriminate five distinct primer design user scenarios, or tasks, that have been integrated in the new interface. These tasks can be selected using a drop down list at the top of the Primer3Plus page. More tasks might be added in future versions of the Primer3Plus web interface. The Detection task can be used for designing standard PCR primers or hybridization oligos to detect a given sequence.
Library Mispriming. End Sequence Quality. Position Penalty. End Stability. Primer failure rate. Product Size. TH: Any Complementarity. TH: 3' End Complementarity. TH: Template Mispriming Weight. Any Complementarity. Tm Difference. Primer Penalty Weight. Internal Oligo Penalty Weight. Internal Oligo Size. Internal Oligo Tm. TH: Internal Oligo Hairpin.
Internal Oligo Self Complementarity. Internal Oligo Min Sequence Quality. Max Ns. Internal Oligo Max Poly-X.
Internal Oligo Mishyb Library. Internal Oligo Max Library Mishyb. Internal Oligo Conc of monovalent cations. Internal Oligo conc of divalent cations. Internal Oligo 3' End Complementarity. Internal Oligo N's. Internal Oligo Library Mishybing. Internal Oligo Sequence Quality. Internal Oligo Sequence End Quality.
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