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.
Citing angsd: Difference between revisions
Jump to navigation
Jump to search
| Line 14: | Line 14: | ||
===SNP calling=== | ===SNP calling=== | ||
SNP calling based on genotype likelihoods | SNP calling based on genotype likelihoods | ||
; - | ; -SNP_pval | ||
[[kim2011]] | [[kim2011]] | ||
Revision as of 01:52, 16 January 2014
Currently there is not publication for angsd. However, many of the methods implemented here are published.
Methods
Maf estimation from counts of alleles
- -cutoff
Allele estimation
allele estimation from genotype likelihoods
- - doMaf
SNP calling
SNP calling based on genotype likelihoods
- -SNP_pval
Genotype likelihoods
- -GL 1
same as in samtools Li2011
- -GL 2
same as in gatk
- -GL 3
same as in soapSNP
- -GL 4
same as in kim2011
Association
- -doAsso 2
using score statistic Skotte2012
- -doAsso 1 or 3
using allele frequencies kim2011
SFS estimation
Estimating the site frequency spectrum Nielsen2012
Neutrality tests (eg Tajima)
Admixture
http://www.popgen.dk/software/index.php/NgsAdmix#Citation
Error rates method 1
joint GL and error estimation kim2011
Error rates method 2
based on a high quality genome orlando2013