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Infer the ancestry proportions from low depth NGS data of a single indivudal. The principal is the same as ngsAdmix, uses a referenece panel of population specific frequencies, also works when you have uncertainty in your data. This makes it ideal for quick and easy analyses of medium and low depth sequencing data samples where many genotypes cannot be called without introducing errors or ascertainment bias. Also a PCA method for taking population structure into account. | Infer the ancestry proportions from low depth NGS data of a single indivudal. The principal is the same as ngsAdmix, uses a referenece panel of population specific frequencies, also works when you have uncertainty in your data. This makes it ideal for quick and easy analyses of medium and low depth sequencing data samples where many genotypes cannot be called without introducing errors or ascertainment bias. Also a PCA method for taking population structure into account. | ||
Revision as of 16:14, 21 February 2017
ANGSD
Analysis of Next Generation Sequencing Data
<classdiagram type="dir:LR"> [sequence data]->[genotype;likelihoods] [genotype;likelihoods]->[genotype;probabilities] [sequence files|bam files;SOAP files{bg:orange}]->[sequence data] [glf files|glfv3;soapSNP{bg:orange}]->[genotype;likelihoods] [genotype prob|beagle output{bg:orange}]->[genotype;probabilities] </classdiagram>
NgsAdmix
Infer the ancestry proportions from low depth NGS data. The principal is the same as other softwares such as FRAPPE and ADMIXTURE however, ngsAdmix also works when you have uncertainty in your data. This makes it ideal for medium and low depth sequencing data where many genotypes cannot be called without introducing errors or ascertainment bias.
fastNGSadmix
Infer the ancestry proportions from low depth NGS data of a single indivudal. The principal is the same as ngsAdmix, uses a referenece panel of population specific frequencies, also works when you have uncertainty in your data. This makes it ideal for quick and easy analyses of medium and low depth sequencing data samples where many genotypes cannot be called without introducing errors or ascertainment bias. Also a PCA method for taking population structure into account.
Relate
This method estimates the probability of sharing alleles identity by descent (IBD) across the genome and can also be used for mapping disease loci using distantly related individuals. To accommodate LD the methods need SNP for several individuals in order to estimate the allele frequencies and the pairwise LD. The method return the posterior probabilities of the IBD states across the genome and the overall IBD sharing.
RelateAdmix
A software package for inferring relatedness between pairs of individuals even if the individuals are admixed.
NgsRelate
A software package for inferring relatedness between pairs of individuals from NGS data.
BAMSE
CATS
R package for power estimation for a two-stage genome-wide association design. This is a modification of the code from Skol et al 2006, nat genet. so that the relative risk, case-control ratios and allele frequencies are allowed to vary between stages.