Hello!!
I want to design PCR primers for 300 contig sequences. For the same, I tried using primer3 standalone. following command I am using to run the tool:
./primer3_core -format_output -default_version=2 -p3_settings_file=settings_file -strict_tags -output=primer3_out contigs.fa
For the above command I get the error: ./primer3_core: Input line with no '=':
settings_file is as below:
Primer3 File - http://primer3.sourceforge.net P3_FILE_TYPE=settings
P3_FILE_ID=Default settings of primer3 version 1.1.4 PRIMER_TASK=generic PRIMER_PICK_LEFT_PRIMER=1 PRIMER_PICK_INTERNAL_OLIGO=0 PRIMER_PICK_RIGHT_PRIMER=1 PRIMER_NUM_RETURN=1 PRIMER_PRODUCT_SIZE_RANGE=100-600 PRIMER_MIN_SIZE=18 PRIMER_OPT_SIZE=22 PRIMER_MAX_SIZE=27 PRIMER_MIN_GC=45.0 PRIMER_OPT_GC_PERCENT=50.0 PRIMER_MAX_GC=58.0 PRIMER_MIN_TM=50.0 PRIMER_OPT_TM=55.0
PRIMER_MAX_TM=60.0
contigs.fa file is as below:
SEQUENCE_ID=c0_g1_i1_len=235_path=[1:0-234] [-1, 1, -2]
SEQUENCE_TEMPLATE=TTTTTGTCTGTCCTGCCCTGTCTGTCTCTCTGTCTCTTTCCAGCTGTGATTCTTCATCTTGTCCTCTCCCCGTCTCTCTCTCTTGCTCTTTATCTCTTTCTCTGCCTCTCTCTGTCATTCTCTCTCTCCCTGGCCCTCTCTGCCCAGATCG
SEQUENCE_ID=c0_g1_i1_len=220_path=[352:0-219] [-1, 352, -2]
SEQUENCE_TEMPLATE=AGATTAAAGCTTGCAAGAGCAGTTTGTAGATTATTTGAGGTAATAGTTTTTATGTTTTCAACAATGATGAAAAGTTTAATCGAAGGATATGGAGGAGAAAGGATCAACTCCACTCATCTGTGCCTACACATAGCTCTCTAAAGGTTGAGGGTAG
Any help for the same will be appreciated.
Thanks!
Thanks Rajesh that was very helpful