ANGSD: Analysis of next generation Sequencing Data

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Supersim: Difference between revisions

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Small program to simulate genotype likelihoods.
Small program to simulate genotype likelihoods.
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./supersim
<pre class="mw-collapsible-content">
./supersim
-> Required arg:
-outfiles PREFIX PREFIX.seq PREFIX.glf PREFIX.frq PREFIX.arg
-> Optional arg:
-npop Number of populations. This MUST be set before -nind [1]
-nind Number of diploid individuals for each population [10]
-nsites Number of sites [500000]
-errate The sequencing error rate [0.0075]
-depth Mean sequencing depth [5]
-pvar Probability that a site is variable in the population [0.015]
-mfreq Minimum population frequency [0.0001]
-F inbreeding coefficient for each population [0]
-model 0=fixed errate 1=variable errate [1]
-simpleRand boolean [1]
-base_freq Background allele frequencies for A,C,G,T [0.25 0.25 0.25 0.25]
</pre>
</div>

Latest revision as of 15:18, 4 December 2015

Small program to simulate genotype likelihoods.

./supersim

./supersim
	 -> Required arg:
		-outfiles PREFIX	 PREFIX.seq PREFIX.glf PREFIX.frq PREFIX.arg
	 -> Optional arg:
		-npop	Number of populations. This MUST be set before -nind [1]
		-nind	Number of diploid individuals for each population [10]
		-nsites	Number of sites [500000]
		-errate	The sequencing error rate [0.0075]
		-depth	Mean sequencing depth [5]
		-pvar	Probability that a site is variable in the population [0.015]
		-mfreq	Minimum population frequency [0.0001]
		-F	inbreeding coefficient for each population [0]
		-model	0=fixed errate 1=variable errate [1]
		-simpleRand	boolean [1]
		-base_freq	Background allele frequencies for A,C,G,T [0.25 0.25 0.25 0.25]