Epistasis simulator of SNP pattern in Windows
Project description
EpistaSim is a simulator that can estimate haplotype frequency and simulate DNA sequences in a region linking with target two loci under haplotype selective model through forward and backward process integrating with mutation and recombination. The output of software was similar with Hudson’s ms software (Hudson, 1990). EpistaSim is a flexible simulator so that it can incorporate different epistasis model. The software runs forward and coalescent simulations depending on the histories (trajectories) of haplotype frequency which was output accompany with DNA sequences of the region in text files. EpistaSim included two parts forward and backward simulation.
Download and Install
Download package “EpistaSim” and unzip
Run cmd and enter the directory of EpistaSim
Loading EpistaSim package, use following command:
python setup.py install
Run EpistaSim
Open the window of python (Commond line) or Python Shell
Forward:
Simulate the DNA sequences and haplotype frequency through forward process, using fowllowing command:
import Forward Forward.main()
- Examples:
import Forward Forward.main() A prompt of input arguments as follow: Enter haplotype frequency split by space: 0.25 0.25 0.25 0.25 Enter Epistasis selective model (If you want to use default value press space key): M1 Enter selective haplotype or allele from two-locus(You must seperate by comma between alleles from two-locus corresponding to M3 or M4; If you want to use default value press space key): 11 Enter selective coefficient (If you specified M3 or M4, input two selective coefficients from two locus seperated by comma; If you want to use default value press space key): 0.01 Enter the number of simulated samples ( If you want to use default value press space key): 10 Enter the number of replication ( If you want to use default value press space key): 5 Enter the length of simulated region ( If you want to use default value press space key): 1000 Enter the number of generation ( If you want to use default value press space key): 200 Enter position of two selective loci split by space ( If you want to use random position press space key): 10 100 Enter recombination rate per generation per bp ( If you want to use default value press space key): Enter mutation rate per generation per bp ( If you want to use default value press space key): 0.0000001 Enter the number of segsites in the region ( If you want to use random value press space key): Enter the outputfile name of simulated sequence: forward.out Enter the outputfile name of haplotype frequency trajectories: hapfre.out The running information of Forward was illustrated as follow: Generate the initial population Print the track file of haplotype frequency Simulation the offspring simulation the 0th replication A region of 1000bp include 12 segsites were simulated for 200 generations with sample size 10 for 1 replication. ..........
Backward:
Simulate the DNA sequences and haplotype frequency through coalescent process, using fowllowing command:
import Backward Backward.main()
Examples
import Backward Backward.main() A prompt of input arguments as follow: Enter haplotype frequency split by space: 0.3 0.1 0.1 0.5 Enter selective haplotype from two-locus(If you want to use default value press space key): 11 Enter selective coefficient ( If you want to use default value press space key): 0.01 Enter the number of simulated samples ( If you want to use default value press space key): 10 Enter the number of replication ( If you want to use default value press space key): 5 Enter the length of simulated region ( If you want to use default value press space key): 1000 Enter position of two selective loci split by space ( If you want to use random position press space key): 10 100 Enter recombination rate per generation per bp ( If you want to use default value press space key): 0.0000001 Enter mutation rate per generation per bp ( If you want to use default value press space key): 0.0000001 Enter the number of segsites in the region ( If you want to use random value press space key): Enter the outputfile name of simulated sequence: backward.out Enter the outputfile name of haplotype frequency trajectories: hapfre.out The running information of Forward was illustrated as follow: Print the track file of haplotype frequency Simulation the offspring simulation the 0th replication A region of 1000bp include 9 segsites were simulated with sample size 10 for 1 replication. ..........
Output of EpistaSim
The outputs of Forward and Backward are the sames and similar with Hudson’s ms software (Hudson, 1990).
According to the up arguments, the results as fowllow:
Output of DNA sequence
// Segsites: 12 Selected two_locus: 10 100 Positions: 10 100 125 158 258 309 472 631 756 818 858 886 111011011111 111011011110 111010010110 111111000111 111001011011 101100011111 001110011111 001000011111 001011011111 011100000001 // ........
Output of haplotype frequency
// T 00 01 10 11 0 0.25 0.25 0.25 0.25 1 0.248079102592 0.253290720757 0.254300434135 0.244329742516 2 0.250079789017 0.260533576401 0.254926425626 0.234460208956 3 0.247683161282 0.257852724706 0.259331708331 0.235132405681 ...... 199 0.174483716477 0.147128461696 0.166087155013 0.512300666814 200 0.175953877557 0.145569161198 0.163958437969 0.514518523277
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