View source: R/ethseq_Analysis.R
| ethseq.Analysis | R Documentation | 
This function performs ancestry analysis of a set of samples ad reports the results.
ethseq.Analysis(
  target.vcf = NA,
  target.gds = NA,
  bam.list = NA,
  out.dir = tempdir(),
  model.gds = NA,
  model.available = NA,
  model.assembly = "hg38",
  model.pop = "All",
  model.folder = tempdir(),
  run.genotype = FALSE,
  aseq.path = tempdir(),
  mbq = 20,
  mrq = 20,
  mdc = 10,
  cores = 1,
  verbose = TRUE,
  composite.model.call.rate = 1,
  refinement.analysis = NA,
  space = "2D",
  bam.chr.encoding = FALSE
)
target.vcf | 
 Path to the sample's genotypes in VCF format  | 
target.gds | 
 Path to the sample's genotypes in GDS format  | 
bam.list | 
 Path to a file containing a list of BAM files paths  | 
out.dir | 
 Path to the folder where the output of the analysis is saved  | 
model.gds | 
 Path to a GDS file specifying the reference model  | 
model.available | 
 String specifying the pre-computed reference model to use  | 
model.assembly | 
 String value indicating the assembly version to download for the pre-build models  | 
model.pop | 
 String value indicating the population to download for the pre-build models  | 
model.folder | 
 Path to the folder where reference models are already present or downloaded when needed  | 
run.genotype | 
 Logical values indicating whether the ASEQ genotype should be run  | 
aseq.path | 
 Path to the folder where ASEQ binary is available or is downloaded when needed  | 
mbq | 
 Minmum base quality used in the pileup by ASEQ  | 
mrq | 
 Minimum read quality used in the piluep by ASEQ  | 
mdc | 
 Minimum read count acceptable for genotype inference by ASEQ  | 
cores | 
 Number of parallel cores used for the analysis  | 
verbose | 
 Print detailed information  | 
composite.model.call.rate | 
 SNP call rate used to run Principal Component Analysis (PCA)  | 
refinement.analysis | 
 Matrix specifying a tree of ancestry sets  | 
space | 
 Dimensions of PCA space used to infer ancestry (2D or 3D)  | 
bam.chr.encoding | 
 Logical value indicating whether input BAM files have chromosomes encoded with "chr" prefix  | 
Logical value indicating the success of the analysis
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