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. 2012 Jun 18:13:134.
doi: 10.1186/1471-2105-13-134.

Primer-BLAST: a tool to design target-specific primers for polymerase chain reaction

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Primer-BLAST: a tool to design target-specific primers for polymerase chain reaction

Jian Ye et al. BMC Bioinformatics. .

Abstract

Background: Choosing appropriate primers is probably the single most important factor affecting the polymerase chain reaction (PCR). Specific amplification of the intended target requires that primers do not have matches to other targets in certain orientations and within certain distances that allow undesired amplification. The process of designing specific primers typically involves two stages. First, the primers flanking regions of interest are generated either manually or using software tools; then they are searched against an appropriate nucleotide sequence database using tools such as BLAST to examine the potential targets. However, the latter is not an easy process as one needs to examine many details between primers and targets, such as the number and the positions of matched bases, the primer orientations and distance between forward and reverse primers. The complexity of such analysis usually makes this a time-consuming and very difficult task for users, especially when the primers have a large number of hits. Furthermore, although the BLAST program has been widely used for primer target detection, it is in fact not an ideal tool for this purpose as BLAST is a local alignment algorithm and does not necessarily return complete match information over the entire primer range.

Results: We present a new software tool called Primer-BLAST to alleviate the difficulty in designing target-specific primers. This tool combines BLAST with a global alignment algorithm to ensure a full primer-target alignment and is sensitive enough to detect targets that have a significant number of mismatches to primers. Primer-BLAST allows users to design new target-specific primers in one step as well as to check the specificity of pre-existing primers. Primer-BLAST also supports placing primers based on exon/intron locations and excluding single nucleotide polymorphism (SNP) sites in primers.

Conclusions: We describe a robust and fully implemented general purpose primer design tool that designs target-specific PCR primers. Primer-BLAST offers flexible options to adjust the specificity threshold and other primer properties. This tool is publicly available at http://www.ncbi.nlm.nih.gov/tools/primer-blast.

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Figures

Figure 1
Figure 1
The Primer-BLAST web interface.
Figure 2
Figure 2
Schematic alignment of mRNA transcript variants from the ZNF419 gene. Numbers indicate the end positions of exons for variant 5. The red lines indicate the primer regions picked by Primer-BLAST. Note that several transcripts differ by 3 nucleotides due to use of slightly different splice sites even though they share same exons (i.e., variant 2 v.s. variant 1, variant 7 v.s. variant 6 and variant 4 v.s. variant 3). The graph is adapted from NCBI gene report (http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&cmd=Retrieve&dopt=full_report&list_uids=79744. Data accessed 11/02/2011).
Figure 3
Figure 3
Example results of designing target-specific primers. Note that while five primer pairs were returned (as shown in graphic summary), due to space limitation, the figure shows details for the first primer pair only. The “Search Summary” link, when clicked, shows the search parameters used as well as the total number of BLAST hits that are generated during the search process (355,744 hits for the current search). Numbers in alignments indicate the start and end positions for primer and target. A dot (.) indicates nucleotide identity to primer sequence. The search was done on 11/02/2011.
Figure 4
Figure 4
Specificity checking of pre-existing primers. This search was performed by entering the forward and reverse primers without entering any template. The primers (forward primer: GTAGGACTGCTCAGTTCAAACAT, reverse primer: ACAGTTACTACACCCGTAAGGC) were obtained from PrimerBank (http://pga.mgh.harvard.edu/primerbank/) on 11/02/2011 using ZNF419 transcript variant 5 (GenBank accession NM_001098494). While the results indicated all 7 transcript variants from the ZNF419 gene have the same amplicons, this figure shows the details only for variants 1 and 5 due to space limitation. The current search generated 11,236 BLAST hits (done on 11/02/2011).
Figure 5
Figure 5
Examples of potential unintended targets for primer pairs generated by QuantPrime and PRIMEGENS. Example targets are extracted from Primer-BLAST specificity checking results for primer pairs generated by QuantPrime or PRIMEGENS (a total of 162 and 116 potential unintended targets were identified for QuantPrime and PRIMEGENS, respectively. See Table 2 for details). The example primers correspond to those underlined in Additional files 1 and 2.

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