Comparing phasing outputs 🧬

Author: Sonia Sarmiento

Description: This repository provides a step-by-step guide to the phasing process, allowing you to easily replicate our results and make informed decisions about the best phasing strategy for your data.

Coding: I used mainly a HPC cluster with bash scripts and R code at the end for plotting.

Introduction

Welcome to this repository, which focuses on the essential task of choosing the best phasing strategy for your genomic data. Specifically, I provide here a thorough comparison of read-based and pedigree phasing. For this purpose, I use individuals with pedigree information and either include it or not during the phasing to perform both types of phasing. Finally, I compare the phasing outcomes with Mendelian Inheritance for validation. The workflow of the phasing process starts with called variants in a VCF and continues as follows:

Filter VCFs
Phase with WhatsHap (either pedigree or read-based phasing)
Filtering to ensure quality
ShapeIt for final phasing (population-based)

After this, you obtain the final phased VCF files for the comparison.

Workflow

Step 1: Filtering VCFs

GATK Best-practices technical filtering, removing masked regions and sequencing depth filtering.

Input: VCF file ($vcf) and reference genome ($ref)
Script: 1_FilteringVCFs.sh
Output: filtered VCF

NOTE: when filtering for sequencing depth, the haploid individual's lower cutoff has to be at least halved in the sexual chromosome only (e.g. males XY in human, females ZW in birds)

Step 2: Phasing with WhatsHap

Whatshap is a software that allows you to phase genomic data, either using only read-based information or using both read-based and pedigree information if you provide a PED file. With this tool, you can phase both single nucleotide polymorphisms (SNPs) and structural variants (SVs), making it a valuable resource for exploring genetic variation in your data. The process of phasing involves grouping variants that are likely to be inherited together, providing insight into the haplotype structure of your sample.

Input: filtered VCF file ($input_vcf), BAM file ($bam), PED file ($ped), reference genome ($ref)
Script: 2_WhatsHap.sh
Output: phased VCF

Step 3: Filtering VCFs for quality

Filtering for minor allele cound (MAC), missing data and excluding indels.

Input: phased VCF ($phased_vcf)
Script: 3_Post-WhatsHap_filtering.sh
Output: filtered vcf ($filter2.recode.vcf.gz)

Step 4: ShapeIt phasing

In this step we phase our genetic data with ShapeIt4 software already phased using WhatsHap because it improves accuracy of haplotype inference and resolves ambiguities in the data, resulting in a more accurate representation of haplotype information for downstream applications (e.g. imputation). Specifically, ShapeIt uses information from multiple individuals to perform population-based phasing. It is important to be aware of its limitations when dealing with related individuals, as it may result in a biased outcome. To avoid this, it is recommended to phase related samples with a reference panel of known unrelated individuals, previously phased with WhatsHap and ShapeIt according to this same workflow. To identify unrelated samples in your dataset, you can follow the guide FindingUnrelated.md in the repository for pedigree analysis.

Input: post-whatshap filtered VCF ($post-whatshap_filtered.vcf), reference genome ($ref)
Script: 4_ShapeIt.sh. More information about the code here.
Output: phased vcf per chromosome / scaffold ($phased_CHR.vcf.gz)

Step 5 (optional): Merging phased datasets

If you have both unrelated and related samples, you can merge both datasets using the following code. Moreover, before merging you would have to intersect SNPs between the two VCFs.

Input: phased vcf (unrelated / related) ($unrelated.vcf.gz/related.vcf.gz)
Script: below
Output: phased merged vcf ($final.vcf.gz)

# Keep intersect snps of unrelated
bcftools isec -n=2 -w1 -O z -o $unrelated_intersectsnps.vcf.gz unrelated.vcf.gz related.vcf.gz

# Keep intersect snps of related
bcftools isec -n=2 -w1 -O z -o $related_intersectsnps.vcf.gz related.vcf.gz unrelated.vcf.gz

# Merge datasets
bcftools merge -O z -o $final.vcf $unrelated_intersectsnps.vcf.gz $related_intersectsnps.vcf.gz

# If you split your dataset per chromosome/scaffold, you can concatenate the files
bcftools concat --threads 8 --file-list $vcf_ordered.list -O z -o $final.vcf.gz
bcftools index  $final.vcf.gz

# Example of $vcf_ordered.list : 
# ${myPATH}/final_CHR1.vcf.gz
# ${myPATH}/final_CHR2.vcf.gz
# ${myPATH}/final_CHR3.vcf.gz

Step 6: Comparing phased VCFs with Mendelian Inheritance

SwitchShapeIt 5 is a code for comparing phased VCF genotypes with Mendelian inheritance to assess phasing accuracy. Here, we use it to compare read-base and pedigree phasing.

Important: This procedure can only be performed on offspring with both unphased parents available for comparison.

Input: phased vcf from offspring (shapeit phased read-base/pedigree), unphased vcf from parents + offsprings (vcfs after 1_FilteringVCFs.sh)
Script: 6_Switch.sh
Output: Switch error rate between Validation (Unphased - Mendelian Inheritance) and Phased VCF. The ouput can be either per sample or per SNP. These are a 4 columns file, with col1=sample_id (for sample.switch.txt.gz only) and col4=switch error rate.

Step 7: Plotting results

Once you have the output files, you can plot the switch error rate per sample using an R code.

Input: $OUTPUT_PREFIX.sample.switch.txt.gz (one per phasing type) --> per sample || $OUTPUT_PREFIX.variant.switch.txt.gz --> per variant
Script: 7_Plotting_persample.R and 7_Plotting_pervariant.R
Output: Plot of Switch Error Rate (y-axis) per sample for each phasing type (x-axis) or per variant along the chromosome (x-axis).

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