Qploidy1.0.1 package

Estimation of Ploidy and Detection of Aneuploidy Using Genotyping Data

all_resolutions_plots

Plot graphics for ploidy visual inspection for each resolution

area_estimate_ploidy

Estimate ploidy using area method

clean_summary

Clean Axiom Summary File

find_header_line

Find the Header Line in a File

get_aneuploids

indexes for aneuploids

get_baf_par

To create baf in parallel

get_baf

Calculate B-Allele Frequency (BAF) from Theta Values

get_centers

Estimate Cluster Centers for Genotype Dosage Classes

get_R_theta

Get R and Theta Values from Summary File

get_zscore

Calculate Z-Scores for Allele Intensities or Counts

merge_arms_format

Merges chromosome-arm level analysis results into chromosome level for...

mode

Calculate the Statistical Mode

pascalTriangle

Pascal Triangle for Expected Peaks Calculation

plot_baf_hist

Plot BAF Histogram

plot_baf

Plot BAF

plot_qploidy_standardization

Plot Method for Qploidy Standardization

print.qploidy_area_ploidy_estimation

print qploidy_area_ploidy_estimation object

print.qploidy_standardization

Print method for object of class 'qploidy_standardization'

qploidy_read_vcf

Convert VCF File to Qploidy Data

read_axiom

Convert Axiom Array Summary File to Qploidy Input

read_illumina_array

Read Illumina Array Files

read_qploidy_standardization

Read Qploidy Standardization File

rm_outlier

Identify and Remove Outliers Based on Bonferroni-Holm Adjusted P-value...

simulate_axiom_summary

Simulate an Axiom array summary file

simulate_illumina_file

Simulate an Illumina File

simulate_standardization_input

Simulate Genotyping Data with Flexible Ploidy

simulate_vcf

Simulate a VCF file with GT, DP, and AD format fields for 2 chromosome...

standardize

Standardize Allelic Ratio Data and Compute BAF and Z-Scores

summary_to_fitpoly

Convert Summary Data to FitPoly-Compatible Format

updog_centers

Estimate Centers for Standardization Using Updog Bias

vcf_sanity_check

Perform a Sanity Check on a VCF File

Provides functions for estimating ploidy levels and detecting aneuploidy in individuals using allele intensities or allele count data from high-throughput genotyping platforms, including single nucleotide polymorphism (SNP) arrays and sequencing-based technologies. Implements an extended version of the 'PennCNV' signal standardization method by Wang et al. (2007) <doi:10.1101/gr.6861907> for higher ploidy levels. Computes B-allele frequencies (BAF), z-scores, and identifies copy number variation patterns.

  • Maintainer: Cristiane Taniguti
  • License: AGPL (>= 3)
  • Last published: 2025-05-01