ANGSD: Analysis of next generation Sequencing Data
Latest tar.gz version is (0.938/0.939 on github), see Change_log for changes, and download it here.
SFS Estimation: Difference between revisions
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0.995120 0.001202 0.000469 0.000255 0.000239 0.000254 0.000125 #capped | 0.995120 0.001202 0.000469 0.000255 0.000239 0.000254 0.000125 #capped | ||
</pre> | </pre> | ||
This is to be interpreted as: | |||
column1 := probabilty of sampling zero derived alleles | |||
column2 := probabilty of sampling one derived allele | |||
column3 := probabilty of sampling two derived allele | |||
column4 := probabilty of sampling three derived allele | |||
etc |
Revision as of 17:23, 10 October 2012
This method will estimate the site frequency spectrum, the method is described in Nielsen2012.
This is a 2 step procedure first generate a ".sfs" file, followed by an optimization of the .sfs file which will estimate the Site frequency spectrum. For the optimization we have implemented 2 different approaches both found in the misc subdir of the root subdir.This is shown in the diagram below.
NB the ancestral state needs to be supplied for this methodd <classdiagram type="dir:LR">
[sequence data]->GL[genotype likelihoods|SAMtools;GATK;SOAPsnp;Kim et.al]
[genotype likelihoods|SAMtools;GATK;SOAPsnp;Kim et.al]->realSFS[.sfs file] [.sfs file]->optimize[.sfs.ml file]
</classdiagram>
- -realSFS 1
- an sfs file will be generated.
- -realSFS 2
- snpcalling (not implemented, in this angsd)
- -realSFS 4
- genotypecalling (not implemented, int this angsd)
options
- -underFlowProtect [INT]
a very basic underflowprotection
Example
A full example is shown below, here we use GATK genotype likelihoods and our reference hg19.fa
#first generate .sfs file ./angsd -bam smallBam.filelist -realSFS 1 -out small -anc hg19.fa -GL 2 #now try the EM optimization with 4 threads ./emOptim.g++ -binput small.sfs -nChr 20 -maxIter 100 -nThread 4 #lets also try the optimization that uses derivates (bfgs) ./optimSFS.gcc small.sfs -nChr 20 -nThreads 4
The outpiles are then called small.sfs.em.ml and small.sfs.ml
0.995120 0.001202 0.000469 0.000255 0.000239 0.000254 0.000125 #capped
This is to be interpreted as:
column1 := probabilty of sampling zero derived alleles column2 := probabilty of sampling one derived allele column3 := probabilty of sampling two derived allele column4 := probabilty of sampling three derived allele etc