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qPCR_pprimer_desigmed

GWAS关联分析找到显著位点

###利用SNP_TransF_genr.v1.1.py 脚本找到多年重复的显著位点的目标基因 python3 SNP_TransF_genr.v1.1.py -i SNP.txt -v test.vcf -o output -g ref.gff

###利用 Extract_seq.py 找到gff文件中目标基因的序列并将其整理成primer3的输入文件 python3 Extract_seq.py

###若是在线网站设计引物则可以将引物信息整理成epcr格式运行 run_epcr.py进行验证 python3 run_epcr.py

利用primer3_with_ePCR_validation.py调用primer3_core和epcr 设计引物并进行引物验证

python3 primer3_with_ePCR_validation.py

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