>arr_1 20,D-loop,F,12S,V,16S,L1,ND1,I,Q,M,ND2,W,A,N,C,Y,COX1,S1,D,COX2,K,ATP8,ATP6,COX3,G,ND3,R,ND4L,ND4,H,S2,L2,ND5,ND6,E,CYTB,T,P >arr_2 18,D-loop,L2,T,P,F,12S,V,16S,L1,ND1,I,Q,M,ND2,W,A,N,C,Y,COX1,S1,D,COX2,K,ATP8,ATP6,COX3,G,ND3,R,ND4L,ND4,H,S2,ND5,ND6,E,CYTB >arr_3 12,D-loop,H,L2,T,P,F,12S,V,16S,L1,ND1,I,Q,M,ND2,W,A,N,C,Y,COX1,S1,D,COX2,K,ATP8,ATP6,COX3,G,ND3,R,ND4L,ND4,S2,ND5,ND6,E,CYTB >arr_4 6,D-loop,H,F,12S,V,16S,L1,ND1,I,Q,M,ND2,W,A,N,C,Y,COX1,S1,D,COX2,K,ATP8,ATP6,COX3,G,ND3,R,ND4L,ND4,S2,L2,ND5,ND6,CYTB,E,T,P >arr_5 1,D-loop,F,12S,V,16S,L1,ND1,I,Q,M,M,ND2,W,A,N,C,Y,COX1,S1,D,COX2,K,ATP8,ATP6,COX3,G,ND3,R,ND4L,ND4,H,S2,L2,ND5,ND6,E,CYTB,T,P ############################################################################################ ## Note: This is the description section. This section only describes the above. # ## In your actual input file, it need to be deleted. # ## 1. >arr_1, >species_1, or >mitogenome_1, it is followed by a newline # ## character to indicate the name of mitochondrial genome arrangement.It # ## is similar to the fasta format. # ## 2.In the next line of the name, two types of information should be entered. # ## (1) The number before the first comma indicates the frequency at which the # ## arrangement type appears, often one or more times (combining the same # ## arrangements is beneficial to increase the calculation speed). # ## (2) The first comma is followed by a certain arrangement of mitochondrial genome, # ## which is separated by commas between the two genes in gene order. # ## In addition, to ensure that comparison tasks can be performed between different # ## arrangement types, each of your data MUST contain all the genes that need to be # ## considered. They should also be consistent with gene name and quantity of the benchmark.# ## If a gene is missed in a certain arrangement, our algorithm will # ## treat it as a gene loss (it Does not include the fact that the phenomenon of gene # ## loss does exist). # ## Because the mitochondrial genome is circular, if the order of the genes is not # ## wrong,the change in gene initiation will not affect the correct output between multiple # ## genome arrangements entered. # ############################################################################################