Entering edit mode
5.3 years ago
mary
▴
210
Hi all
Sorry if it is a basic question
I am studying on ROH in some European sheep breed. Runs of homozygosity were defined for individuals in each of populations using PLINK v1.9. To identify the genomic regions that were most commonly associated with ROH (ROH Islands), the percentage of the occurrences of a SNP in ROH should be calculated by counting the number of times the SNP was detected in those ROH across individuals. How can I count the number of time the SNP appearance on ROH?
The Results file contain following item
FID IID PHE CHR SNP1 SNP2 POS1 POS2 KB NSNP DENSITY PHOM PHET
APD APD_1 -9 5 OAR5_35572649.1 OAR5_38405078.1 32051539 34648887 2597.349 56 46.381 0.982 0.018
APD APD_1 -9 16 OAR16_15286536.1 OAR16_18306489.1 14045257 16664181 2618.925 48 54.561 0.979 0.021
APD APD_1 -9 26 s13893.1 OAR26_50043613.1 41264092 43975533 2711.442 55 49.299 0.982 0.018
APD APD_1 -9 18 s73454.1 OAR18_50990546_X.1 44885240 47744975 2859.736 55 51.995 0.982 0.018
APD APD_1 -9 4 s31519.1 OAR4_89501743.1 81401534 84288706 2887.173 57 50.652 1 0
APD APD_1 -9 1 OAR1_71742338.1 s03807.1 67130818 70024750 2893.933 51 56.744 1 0
APD APD_1 -9 10 OAR10_24992778.1 OAR10_28010599.1 25053948 27970755 2916.808 50 58.336 1 0
I hope some one help me