ANGSD: Analysis of next generation Sequencing Data
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Citing angsd
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There is an overall angsd paper with bibtex below.
@article{korneliussen_angsd:_2014,
title = {{ANGSD}: Analysis of Next Generation Sequencing Data},
volume = {15},
copyright = {http://creativecommons.org/licenses/by/2.0/},
issn = {1471-2105},
shorttitle = {{ANGSD}},
url = {http://www.biomedcentral.com/1471-2105/15/356/abstract},
doi = {10.1186/s12859-014-0356-4},
abstract = {High-throughput {DNA} sequencing technologies are generating vast amounts of data. Fast, flexible and memory efficient implementations are needed in order to facilitate analyses of thousands of samples simultaneously.},
language = {en},
number = {1},
urldate = {2014-11-26},
journal = {{BMC} Bioinformatics},
author = {Korneliussen, Thorfinn S. and Albrechtsen, Anders and Nielsen, Rasmus},
month = nov,
year = {2014},
pages = {356},
}
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
Contamination
from X chromosome Rasmussen2011