You signed in with another tab or window. Reload to refresh your session.You signed out in another tab or window. Reload to refresh your session.You switched accounts on another tab or window. Reload to refresh your session.Dismiss alert
Judging from your command it seems that most variatns get filtered because their allele frequency falls below/above the thresholds you have defined. What happens when you change the --min-af and --max-af arguments?
HI,
I try to draw a manhattan plot, my plot just shows 300 SNP
my input file is the output file of pyseer( T304_SNPs_02_98.txt),
how can I find the input file with all of the SNP and with P value (not only the phenotype associated ones)?
My command:
pyseer --phenotypes T304_list.txt --vcf core.vcf.gz --load-m T304_mash_mds.pkl --lineage --print-samples --min-af 0.02 --max-af 0.98 > T304_SNPs_02_98.txt
15949 loaded variants
15625 pre-filtered variants
324 tested variants
324 printed variants
cat <(echo "#CHR SNP BP minLOG10(P) log10(p) r^2") <(paste <(sed '1d' T304_SNPs_02_98.txt | cut -d "_" -f 2) <(sed '1d' T304_SNPs_02_98.txt | cut -f 4) | awk '{p = -log($2)/log(10); print "26",".",$1,p,p,"0"}' ) | tr ' ' '\t' > T304_SNPs_02_98.plot
Waiting for your emails,
All the best,
The text was updated successfully, but these errors were encountered: