Has anyone use this software before?
I am new in pcr primer design and want to design primers for rt-pcr. This software has involve chossing of exon-exon junction for users so i thinking to use it. But, how does it compared with primer3? which is better?
thanks
primer-blast from ncbi
Started by wntiong, Nov 24 2009 05:25 PM
3 replies to this topic
#1
Posted 24 November 2009 - 05:25 PM
#2
Posted 24 November 2009 - 05:57 PM
wntiong, on Nov 24 2009, 05:25 PM, said:
Has anyone use this software before?
I am new in pcr primer design and want to design primers for rt-pcr. This software has involve chossing of exon-exon junction for users so i thinking to use it. But, how does it compared with primer3? which is better?
thanks
I am new in pcr primer design and want to design primers for rt-pcr. This software has involve chossing of exon-exon junction for users so i thinking to use it. But, how does it compared with primer3? which is better?
thanks
I think primer-blast is the best site around these days. It implements the original Primer3 algorithm. However, one difference is the annealing temperature calculation, while Primer3 was always a bit too high (you'd have to input 62C to get a primer for 60C), Primer-Blast is correct. Recommended!
Cheers,
Minna
I got soul, but I'm not a soldier
#3
Posted 24 November 2009 - 10:06 PM
wntiong, on Nov 24 2009, 09:25 PM, said:
Has anyone use this software before?
I am new in pcr primer design and want to design primers for rt-pcr. This software has involve chossing of exon-exon junction for users so i thinking to use it. But, how does it compared with primer3? which is better?
thanks
I am new in pcr primer design and want to design primers for rt-pcr. This software has involve chossing of exon-exon junction for users so i thinking to use it. But, how does it compared with primer3? which is better?
thanks
For me, I used PerlPrimer software to design the primer for real-time. You can google it to find the download link.
#4
Posted 25 November 2009 - 12:47 AM
Thanks guys,
i used both primer3 and primer-blast to design primer for same gene, then blast both forward and reverse primer sequences. Apparently two different set of primers were produced and after blast, the primer3's primers showed e value of 0.0015 to that gene's genomic sequence and about e value = 248 for the next genes. for primer-blast's primers showed same e value of 0.0015, but if against to next other gene, it is about 3.5 of e value.
i am not sure. but since the primer-blast has the option to find the exon-exon boundary, which is better according to above blast results?
i am really a beginner onto this, kindly advise though if the question sounds stupid. lol.
thanks
i used both primer3 and primer-blast to design primer for same gene, then blast both forward and reverse primer sequences. Apparently two different set of primers were produced and after blast, the primer3's primers showed e value of 0.0015 to that gene's genomic sequence and about e value = 248 for the next genes. for primer-blast's primers showed same e value of 0.0015, but if against to next other gene, it is about 3.5 of e value.
i am not sure. but since the primer-blast has the option to find the exon-exon boundary, which is better according to above blast results?
i am really a beginner onto this, kindly advise though if the question sounds stupid. lol.
thanks














