1,102
edits
Changes
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input VCF file b pl.genotypes.bcf
input VCF file b pl.genotypes.bcf
input VCF file c st.genotypes.bcf <br>
input VCF file c st.genotypes.bcf <br>
A: 97274 variants
B: 95458 variants
B: 95458 variants
C: 98943 variants <br>
C: 98943 variants <br>
no [ts/tv] [ins/del]
A-- 3887 [1.10] [0.86]
A-- 3887 [1.10] [0.86]
-B- 7890 [1.45] [0.98]
-B- 7890 [1.45] [0.98]
A-C 7458 [1.78] [0.49]
A-C 7458 [1.78] [0.49]
-BC 1639 [1.63] [1.03]
-BC 1639 [1.63] [1.03]
ABC 81569 [2.28] [1.08]
ABC 81569 [2.28] [1.08] <br>
Unique variants : 115080
Overall concordance : 70.88% (#intersection/#union)
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