Last updated: 2025-07-01
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locust-comparative-genomics/
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Modified: data/orthofinder/Schistocerca/Results_I2/Plots_Schistocerca/VerticalStackedBar_cubense.pdf
Modified: data/orthofinder/Schistocerca/Results_I2/Plots_Schistocerca/VerticalStackedBar_gregaria.pdf
Modified: data/orthofinder/Schistocerca/Results_I2/Plots_Schistocerca/VerticalStackedBar_nitens.pdf
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Erez, Olga and their team, have created Hi-C library from 44 samples of the genus Schistocerca from Hojun’s ethanol collection. We want to use the common SNPs from these species to assess the phylogenetic relationship of Schistocerca using genome-wide variants.
[ASK OLGA TO ADD MORE DETAILS ABOUT SEQUENCING AND READS
PREPROCESSING]. The reads were then mapped against S.
piceifrons genome and hard filtered using Dragen at
BCM.
From the vcf header we can see that Dragen, a variant
call
DRAGENCommandLine=<ID=HashTableBuild,Version="SW: 01.003.044.3.10.11, HashTableVersion: 8",
CommandLineOptions="dragen --build-hash-table true --ht-num-threads 40 --ht-mem-limit 32Gb --ht-reference ./reference/GCF_021461385.2_iqSchPice1.1_genomic.fna --output-dir ./reference"
DRAGENCommandLine=<ID=dragen,Version="SW: 07.021.624.3.10.11, HW: 07.021.624",Date="Mon Feb 10 16:06:12 CST 2025",
CommandLineOptions="-r ./reference --fastq-list all_fastq.csv --fastq-list-sample-id HIC17106 --output-directory ./vc_HIC17106 --output-file-prefix HIC17106 --enable-auto-multifile false --combine-samples-by-name false --enable-map-align true --enable-sort false --enable-variant-caller true --enable-duplicate-marking true --enable-map-align-output false --output-format bam --Aligner.unpaired-pen=0 --enable-vcf-indexing false"Then the data was filtered so that the SNP quality must be higher than 10.41, and indel higher than 7.83. The depth of each variant must be at least of 1.
FILTER=<ID=DRAGENSnpHardQUAL,Description="Set if true:QUAL < 10.41">
FILTER=<ID=DRAGENIndelHardQUAL,Description="Set if true:QUAL < 7.83">
FILTER=<ID=LowDepth,Description="Set if true:DP <= 1">
FILTER=<ID=PloidyConflict,Description="Genotype call from variant caller not consistent with chromosome ploidy">
FILTER=<ID=RMxNRepeatRegion,Description="Site filtered because all or part of the variant allele is a repeat of the reference">The data was shared via Dropbox and to transfer them directly to GRACE clusterm we followed the steps mentionned below:
file_links.txt and replace the dl=0 with
dl=1https://www.dropbox.com/scl/fo/a3hvph0rop31gtaoucj8v/AC5daUrN-dBAydjSKdvq3KE/HIC17106.hard-filtered.vcf.gz?rlkey=0bkducf1e7pxil6fi3sdb7fat&dl=0
https://www.dropbox.com/scl/fo/a3hvph0rop31gtaoucj8v/AIun42Q_haxfprCT6QjHmUA/HIC17107.hard-filtered.vcf.gz?rlkey=0bkducf1e7pxil6fi3sdb7fat&dl=0
https://www.dropbox.com/scl/fo/a3hvph0rop31gtaoucj8v/AIaUDoe9_0kzXsr1wCYKoHo/HIC17108.hard-filtered.vcf.gz?rlkey=0bkducf1e7pxil6fi3sdb7fat&dl=0
(...)https://www.dropbox.com/scl/fo/a3hvph0rop31gtaoucj8v/AC5daUrN-dBAydjSKdvq3KE/HIC17106.hard-filtered.vcf.gz?rlkey=0bkducf1e7pxil6fi3sdb7fat&dl=1
https://www.dropbox.com/scl/fo/a3hvph0rop31gtaoucj8v/AIun42Q_haxfprCT6QjHmUA/HIC17107.hard-filtered.vcf.gz?rlkey=0bkducf1e7pxil6fi3sdb7fat&dl=1
https://www.dropbox.com/scl/fo/a3hvph0rop31gtaoucj8v/AIaUDoe9_0kzXsr1wCYKoHo/HIC17108.hard-filtered.vcf.gz?rlkey=0bkducf1e7pxil6fi3sdb7fat&dl=1
(...)wget --no-check-certificate "https://www.dropbox.com/scl/fo/a3hvph0rop31gtaoucj8v/AKkVh4m_l_VtHP8zTHcPlyM?e=2&preview=HIC17106.hard-filtered.vcf.gz&rlkey=0bkducf1e7pxil6fi3sdb7fat&st=wihwy6ah&dl=1" -O HIC17106.hard-filtered.vcf.gzor use directly the file_links.txt:
wget --no-check-certificate -i file_links.txt
for file in *.vcf.gz\?*; do
mv "$file" "$(echo "$file" | cut -d'?' -f1)"
done
# then because the files will appears with their link names, run the following renaming command
for file in *\?*; do
clean=$(echo "$file" | sed "s/'//g" | sed 's/\?.*//')
mv "$file" "$clean"
donesrun --ntasks 1 --cpus-per-task 16 --mem 50G --time 04:00:00 --pty bash
ml GCC/13.2.0 BCFtools/1.19
# Loop over each .vcf.gz file
for vcf in *.hard-filtered.vcf.gz; do
echo "Indexing $vcf..."
bcftools index --csi --threads 16 "$vcf"
doneWe created a Snakemake pipeline to streamlined the further VCF
merging, common SNPs filtering and fasta files. We just need to launch
the first part of our Snakemake file using
sbatch snakemake.slurm
#!/bin/bash
#SBATCH --job-name=snakemake
##SBATCH --partition=short
#SBATCH --time="7-00:00:00"
#SBATCH --mem=50GB
#SBATCH --cpus-per-task=1
#SBATCH --ntasks=1
#module load GCC/11.2.0 OpenMPI/4.1.1 snakemake/6.10.0
ml GCC/11.3.0 OpenMPI/4.1.4 snakemake/7.22.0
snakemake --latency-wait 3600 --restart-times 1 -j 200 -p \
--max-jobs-per-second 1 \
--cluster-config cluster.json \
--cluster "sbatch -p {cluster.partition} --ntasks {cluster.ntasks} --cpus-per-task {cluster.cpus-per-task} -t {cluster.time} --mem {cluster.mem}" \
--notemp --nolock \
--rerun-incompleteand at the moment we are interested in the rules that merge, and keep only biallelic SNPs with a minimum allele count of 1. All indels will be filtered out and we will compute the stats to decide further filtering of sites with high missingness.
### =================================================================
### MERGE VCFs
### =================================================================
rule merge_vcfs:
input:
vcfs = expand("{workdir}/00-raw-vcf/{sample}.hard-filtered.vcf.gz",
sample=config["VCF_SAMPLES"], workdir=config["WORKDir"]),
indices = expand("{workdir}/00-raw-vcf/{sample}.hard-filtered.vcf.gz.csi",
sample=config["VCF_SAMPLES"], workdir=config["WORKDir"])
output:
vcf = config["WORKDir"] + "/01-merged-vcf/all_samples.vcf.gz",
index = config["WORKDir"] + "/01-merged-vcf/all_samples.vcf.gz.csi"
shell:
"""
module purge
ml GCC/13.2.0 BCFtools/1.19
bcftools merge --force-samples -Oz -o {output.vcf} {input.vcfs}
bcftools index -c {output.vcf}
"""
### =================================================================
### FILTER MERGED VCF (biallelic SNPs, no indels, MAC=1, missing<60%)
### =================================================================
rule filter_snps:
input:
vcf = config["WORKDir"] + "/01-merged-vcf/all_samples.vcf.gz"
output:
vcf = config["WORKDir"] + "/02-filtered-vcf/filtered_snps.vcf.gz",
index = config["WORKDir"] + "/02-filtered-vcf/filtered_snps.vcf.gz.csi"
params:
cutoff = "--max-meanDP 14",
filters = "--remove-indels --minDP 4 --minQ 30 --max-missing 0.7 --max-alleles 2",
span = "--chr NC_060138.1 --chr NC_060139.1 --chr NC_060140.1 --chr NC_060141.1 --chr NC_060142.1 --chr NC_060143.1 --chr NC_060144.1 --chr NC_060145.1 --chr NC_060146.1 --chr NC_060147.1 --chr NC_060148.1 --chr NC_060149.1"
shell:
"""
module purge
ml GCC/13.2.0 VCFtools/0.1.16 BCFtools/1.19
vcftools --gzvcf {input.vcf} {params.span} {params.filters} {params.cutoff} --recode --recode-INFO-all --stdout | bgzip --threads 4 > {output.vcf}
bcftools index -c {output.vcf}
"""
### =================================================================
### SNP STATS REPORT
### =================================================================
rule stats_snps:
input:
vcf = config["WORKDir"] + "/02-filtered-vcf/filtered_snps.vcf.gz"
output:
depth = config["WORKDir"] + "/02-filtered-vcf/snps.depth",
site_depth = config["WORKDir"] + "/02-filtered-vcf/snps.ldepth.mean",
miss_indv = config["WORKDir"] + "/02-filtered-vcf/snps.imiss",
miss_site = config["WORKDir"] + "/02-filtered-vcf/snps.lmiss"
params:
span = "--chr NC_060138.1 --chr NC_060139.1 --chr NC_060140.1 --chr NC_060141.1 --chr NC_060142.1 --chr NC_060143.1 --chr NC_060144.1 --chr NC_060145.1 --chr NC_060146.1 --chr NC_060147.1 --chr NC_060148.1 --chr NC_060149.1"
shell:
"""
module purge
ml GCC/13.2.0 VCFtools/0.1.16
echo "Calculating depth..."
vcftools --gzvcf {input.vcf} {params.span} --depth --out {config[WORKDir]}/02-filtered-vcf/snps
echo "Calculating site mean depth..."
vcftools --gzvcf {input.vcf} {params.span} --site-mean-depth --out {config[WORKDir]}/02-filtered-vcf/snps
echo "Calculating individual missing data..."
vcftools --gzvcf {input.vcf} {params.span} --missing-indv --out {config[WORKDir]}/02-filtered-vcf/snps
echo "Calculating site missing data..."
vcftools --gzvcf {input.vcf} {params.span} --missing-site --out {config[WORKDir]}/02-filtered-vcf/snps
"""
So we have merged the snps.
module purge
ml GCC/12.3.0 vcflib/1.0.9-R-4.3.2 BCFtools/1.18
we will subsample the number of snps so we can run the stats on it
bcftools view all_samples.vcf.gz | vcfrandomsample -r 0.02 > all_samples_subset.vcf
module purge
ml GCC/13.2.0 OpenMPI/4.1.6 R_tamu/4.4.1
export R_LIBS=$SCRATCH/R_LIBS_USER/
library(tidyverse)
library(ggplot2)
# Load and parse data
var_depth <- read_delim("all_samples.ldepth.mean", delim = "\t",
col_names = c("chr", "pos", "mean_depth", "var_depth"), skip = 1)
# Compute the mean
summary(var_depth$mean_depth)
mean_val <- mean(var_depth$mean_depth, na.rm = TRUE)
# Base plot with vertical mean line
a <- ggplot(var_depth, aes(mean_depth)) +
geom_density(fill = "dodgerblue1", colour = "black", alpha = 0.3) +
geom_vline(xintercept = mean_val, colour = "red", linetype = "dashed") +
theme_light()
# Open a multi-page PDF
pdf("mean_depth_density.pdf", width = 6, height = 4)
# Page 1: full density plot
print(a)
# Page 2: zoomed in
a_zoom <- a + xlim(0, 100)
print(a_zoom)
# Close device
dev.off()
###############
# Load missingness data
var_miss <- read_delim("all_samples.lmiss", delim = "\t",
col_names = c("chr", "pos", "nchr", "nfiltered", "nmiss", "fmiss"),
skip = 1)
# Calculate mean missingness
summary(var_miss$fmiss)
mean_fmiss <- mean(var_miss$fmiss, na.rm = TRUE)
# Base plot with vertical mean line
a <- ggplot(var_miss, aes(fmiss)) +
geom_density(fill = "dodgerblue1", colour = "black", alpha = 0.3) +
geom_vline(xintercept = mean_fmiss, colour = "red", linetype = "dashed") +
theme_light()
# Open multi-page PDF
pdf("variant_missingness.pdf", width = 6, height = 4)
# Page 1: full density plot
print(a)
# Page 2: zoomed in
a_zoom <- a + xlim(0, 1) # fmiss is a fraction (0–1), not 0–100
print(a_zoom)
# Close device
dev.off()
###############
# Load individual depth data
ind_depth <- read_delim("all_samples.idepth", delim = "\t",
col_names = c("ind", "nsites", "depth"), skip = 1)
# Calculate mean depth per individual
mean_depth <- mean(ind_depth$depth, na.rm = TRUE)
# Create histogram with vertical mean line
a <- ggplot(ind_depth, aes(depth)) +
geom_histogram(fill = "dodgerblue1", colour = "black", alpha = 0.3, bins = 30) +
geom_vline(xintercept = mean_depth, colour = "red", linetype = "dashed") +
theme_light()
# Open PDF for two pages
pdf("individual_depth_distribution.pdf", width = 6, height = 4)
# Page 1: full view
print(a)
# Page 2: zoomed in (e.g., 0 to 100)
a_zoom <- a + xlim(0, 100)
print(a_zoom)
# Close the PDF device
dev.off()
##################
# Load individual missingness data
ind_miss <- read_delim("all_samples.imiss", delim = "\t",
col_names = c("ind", "ndata", "nfiltered", "nmiss", "fmiss"),
skip = 1)
# Calculate mean missingness
mean_fmiss <- mean(ind_miss$fmiss, na.rm = TRUE)
# Create histogram with vertical line
a <- ggplot(ind_miss, aes(fmiss)) +
geom_histogram(fill = "dodgerblue1", colour = "black", alpha = 0.3, bins = 30) +
geom_vline(xintercept = mean_fmiss, colour = "red", linetype = "dashed") +
theme_light()
# Save to multi-page PDF
pdf("individual_missingness_distribution.pdf", width = 6, height = 4)
# Page 1: full histogram
print(a)
# Page 2: zoomed-in view
a_zoom <- a + xlim(0, 1)
print(a_zoom)
# Close PDF device
dev.off()
sessionInfo()R version 4.4.2 (2024-10-31)
Platform: aarch64-apple-darwin20
Running under: macOS Sequoia 15.5
Matrix products: default
BLAS: /Library/Frameworks/R.framework/Versions/4.4-arm64/Resources/lib/libRblas.0.dylib
LAPACK: /Library/Frameworks/R.framework/Versions/4.4-arm64/Resources/lib/libRlapack.dylib; LAPACK version 3.12.0
locale:
[1] en_US.UTF-8/en_US.UTF-8/en_US.UTF-8/C/en_US.UTF-8/en_US.UTF-8
time zone: Asia/Tokyo
tzcode source: internal
attached base packages:
[1] stats graphics grDevices utils datasets methods base
loaded via a namespace (and not attached):
[1] vctrs_0.6.5 cli_3.6.5 knitr_1.50 rlang_1.1.6
[5] xfun_0.52 stringi_1.8.7 promises_1.3.3 jsonlite_2.0.0
[9] workflowr_1.7.1 glue_1.8.0 rprojroot_2.0.4 git2r_0.36.2
[13] htmltools_0.5.8.1 httpuv_1.6.16 sass_0.4.10 rmarkdown_2.29
[17] tibble_3.3.0 evaluate_1.0.4 jquerylib_0.1.4 fastmap_1.2.0
[21] yaml_2.3.10 lifecycle_1.0.4 whisker_0.4.1 stringr_1.5.1
[25] compiler_4.4.2 fs_1.6.6 pkgconfig_2.0.3 Rcpp_1.0.14
[29] rstudioapi_0.17.1 later_1.4.2 digest_0.6.37 R6_2.6.1
[33] pillar_1.10.2 magrittr_2.0.3 bslib_0.9.0 tools_4.4.2
[37] cachem_1.1.0