Tools for inferring ploidy levels, testing for aneuploidy and other stuff. Calculating its allele frequencies and genotype likelihoods requires to download the followings:

• python 3, with packages gzip, numpy, scipy, pandas, lmfit
• R, with packages pracma, data.table, Rcpp, getopt
• samtools

Overview: simulate poliploidy organisms and output them in an mpileup.gz format

simulationScript.sh -p $FILE -d $DEPTH -l $LOCI -o $OUTNAME

• -p or --ploidyFile: file containing the desired simulated data (see below for the sintax). Each line of the ploidyFile contains the ploidy number and the number of individuals for $K$ adjacent segments of a number $J$ of genomes. Example: $K=3$ adjacent segments and $20$ genomes. The first segment is diploid for all $20$ genomes, the second with is diploid for 10 genomes and tetraploid for 10 genomes, and the third is triploid for all genomes.

2x20
2x10,4x10
3x20

The length of each segment is expressed by the --loci parameter below.

• -l or --loci: sequence of $K$ number of loci $l_1,l_2,...,l_K$ used in each simulated segment of the genomes.
• -d or --depth: vector of haploid depths to simulate. For each depth, a compressed mpileup file is created.
• -o or --out: output file name (without extension). Default: out

One .mpileup.gz file for each haploid depth, number of individuals $N$, with the name $OUTNAME.DP$depth.mpileup.gz.

$SOFTWAREPATH/simulationScript.sh -p ploidy.file -d 10,20 -l 1000,1000,1000 -o outFile

with the file ploidy.file containing

2x20
2x10,4x10
3x20

The output will consists of two files: outFile.DP10.mpileup.gz and outFile.DP20.mpileup.gz

Overview: calculate genotype likelihoods

Genotype_Likelihoods.py names.filelist

• The file names.filelist, that contains the prefix of each file (that is, the name of each file including the extension), for example:

file1.mpileup.gz
file2.mpileup.gz
file3.mpileup.gz

for the files file1.mpileup.gz, file2.mpileup.gz, file3.mpileup.gz. Supported file types are 'bam','mpileup' and 'mpileup.gz' (gzipped mpileup file).

• -o or --outFolder: Output folder. Default: the folder of each input files
• -i or --Inbreeding: Inbreeding coefficients for each sample accepted as a comma seperated list e.g 0.3,0.2,0.1 alternatively can take in the format 0.2x3,0.4 which is equivilent to 0.2,0.2,0.2,0.4. All values must be between 0 and 1. Default value is 0xNSAMS
• -p or --ploidyFile: File containing the list of ploidy levels to be used in analysis, that contains one ploidy level per line, for example:

2
4
5

for diploidy (2), tetraploidy (4) and pentaploidy (5). If not set, default ploidy levels [1, 2, 3, 4, 5, 6] will be used in the analysis.

• -d or --downsampling: Fraction of the data to be included included in the calculation of genotype likelihoods and aneuploidy inference. That is for a value v in (0,1] for each read there is a vx100% chance the base is included in the calculations. this can be used to speed up calculations for high coverage samples. Be careful using this argument for low coverage data. Default: 1
• -m or --min_non_major_freq: Set the minimum frequency of non major alleles for bases to be included in the calculations. Default: 0.2
• -M2 or --max_minor2_freq: Set the maximum frequency of third most prolific alleles for bases to be included in the calculations. Used to determine strengh of confidence on bases being biallelic. Default: 0.1
• -M3 or --max_minor3_freq: Set the maximum frequency of fourth most prolific alleles for bases to be included in the calculations. Used to determine strengh of confidence on bases being biallelic. Default: 0.1
• -dp or --min_global_depth: Set the minimum global depth of a base to be included in calculations. All bases with more than this number of reads, after filtering for other conditions mentioned above, across all bases will be included.
• -dpInd or --min_ind_depth: Set the minimum depth of a base for each sample to included those in the calculations. A locus is not considered if one or more samples have depth lower than the minimum. Default: 0.
• -s or --random_seed: Set the random seed to be included in the calculations. If not set, every repeat of analysis will give different results.
• -r or --ref_fasta: File name of the reference fasta file. Use this if bam files are being used. e.g TAIR10.fa.

A .genolikes.gz file for each prefix in the input file. The columns of the file represent: chromosome name, site number, individual number, ref.allele, site coverage, major allele, minor allele, major allele counts, minor allele counts, genotype likelihoods at ploidy 1 (2 columns), genotype likelihoods at ploidy 2 (3 columns), ..., genotype likelihoods at ploidy 8 (9 columns)

python3 Genotype_Likelihoods.py names.filelist -p ploidyFile -i 0.1x7,0.15,0.1x2 -d 0.9 -m 0.2 -M2 0.15 -M3 0.1 -dp 5 -s 1

Overview: infer ploidy levels of each individual in a .genolikes file (uncompressed file from the output of the Genotype_Likelihoods.py script) using sequencing coverage and genotype likelihoods.

Rscript HMMploidy.R fileList=$FILELIST wind=$WIND 

• fileList: list of base names of files with formats .genolikes, uncompressed from the output of Genotype_Likelihoods.py. Alternatively, use file and write directly the prefix of the desired file that has format .genolikes. For example

file1
file2

for the files file1.genolikes, file2.genolikes.

• wind: windows size, i.e. nr of loci whose means and genotype likelihoods are summed together
• maxPloidy: max number of ploidy levels (default 6)
• nameFile: file with names of all the individuals in the genotype likelihoods file (default: names are ind1, ind2, ...). For example

Cryptococcus
Streptococcus

will be used as names for the first and the second individual of the input file. This will work if the genotype likelihood files have the same number of individuals.

• chosenInd: comma separated indices of individuals to analyze (default: analyzes all individuals). For example chosenInd=1,2,7 to choose the first, second and seventh individual.
• quantileTrim: comma separated values of 2 quantiles to trim depth values. (default 0,1 = keep all data)
• minInd: min number of individuals with data for which a locus is considered in the analysis (default 1)
• eps: sequencing/mapping error rate (default 0.0005)

Note:

• if working on simulations, the list of basenames is already given in output by the simulation script.
• the .genolikes.gz files given in output by the Genotype_Likelihoods.py script must be gunzipped.

For each base name, there are two outputs:

• a .pdf file with inferred ploidy numbers for each individual
• a .HMMploidy file where, for each individual, results are arranged on lines as it follows:
  • File name and sample name
  • starting probability vector $\delta$ of inferred ploidy numbers
  • transition matrix $A$ printed on one line (column by column)
  • $\alpha$ vector of parameters for the depth distribution
  • $\beta$ vector of parameters for the depth distributions
  • final loglikelihood of the model
  • inferred ploidy numbers of the model
  • posterior probabilities for the inferred states (column by column)
  • proportion of posterior probability for each inferred ploidy number
  • starting locus of each window of SNPs
  • ending locus of each window of SNPs
  • inferred ploidy level in each of the windows defined in the two lines above

Simulate 5 genomes ina file called poliploidyGenome, with 4 segments having ploidy numbers 2-5-4-2 for all genomes, and simulating two different haploid depths, 3X and 8X. Consider 1000 simulated loci for each segment. Let SOFTWAREPATHPATH be the folder containing the scripts of this repository.

Simulate the dataset

$SOFTWAREPATHPATH/simulationScript.sh -p ploidy.file -d 3,8 -l 1000,1000,1000,1000 -o poliploidyGenome

with the file ploidy.file containing:

2x5
5x5
4x5
2x5

There are two simulated .mpileup.gz files in output: poliploidyGenome.DP3.mpileup.gz, poliploidyGenome.DP8.mpileup.gz, and a file containing the list of prefixes for calculating the genotype likelihoods: poliploidyGenome.filelist

Calculate genotype likelihoods without applying any filter (see the script options for filtering details):

python3 $SOFTWAREPATHPATH/Genotype_Likelihoods.py poliploidyGenome.filelist

Run the analysis of ploidy numbers for the two simulated datasets. Use window size 100, analyze all the individuals, consider the max ploidy number being 5, do not trim the data, and use loci where there is data for >=2 individuals

gunzip *.genolikes.gz #the R script needs gunzipped genolikes files
Rscript $SOFTWAREPATHPATH/HMMploidy.R  fileList=poliploidyGenome.filelist  maxPloidy=5  wind=100  minInd=2

In output you will find the pdf files poliploidyGenome.DP4.pdf,poliploidyGenome.DP8.pdf with a fancy plot of the inferred ploidy for each individual and the mean depth of each window. The text output is contained in the files poliploidyGenome.DP4.HMMploidy,poliploidyGenome.DP8.HMMploidy

Each .genolikes file given in input to HMMploidy.R is expected to have only one chromosome. However, in presence of more chromosomes/contigs, the software will automatically analyze the contigs as adjacent in a whole genome fashion. Windows of loci will be done in each chromosome/contig to avoid sharing loci in a window between chromosomes/contigs. Windows will be downsized in chromosomes/contigs not large enough, and chromosomes/contigs without SNPs will be automatically removed from the analysis.