Detect complex regions¶

Synopsis¶

Human chromosomes have large regions of highly identical repeats. They can be found in as clusters centromeres, regions of segmental duplication, or in the acrocentric short arms of chromosomes. Logsdon et al., Nature 2021 showed that chromosome 8 carries a modestly sized centromere of approximately 1.5–2.2 Mb, in which AT-rich, 171-base-pair (bp) α-satellite repeats are organized into a well-defined higher-order repeat (HOR) array. odgi offers tools to detect and explore such regions.

Steps¶

Get the Human chr8 dataset¶

Download the pangenome graph of the Human chromosome 8 in GFA format, decompress it, and convert it to a graph in odgi format:

wget -c https://s3-us-west-2.amazonaws.com/human-pangenomics/pangenomes/scratch/2021_05_06_pggb/gfas/chr8.pan.gfa.gz
gunzip chr8.pan.gfa.gz

odgi build -g chr8.pan.gfa -o chr8.pan.og --threads 2 -P

The last command creates a file called chr8.pan.og, which contains the input graph in odgi format. This graph contains the contigs of 88 haploid, phased human genome assemblies from 44 individuals, plus the chm13 and GRCh38 reference genomes.

Obtain the depth over the pangenome¶

To identify the repetitive sequences, we can analyze the depth in the graph. Here we define as node depth the number of times in which the node is crossed by all the paths present in the graph.

To obtain the depth over the pangenome graph, execute:

odgi depth -i chr8.pan.og -r chm13#chr8 | \
    bedtools makewindows -b /dev/stdin -w 5000 > chm13.chr8.w5kbps.bed

odgi depth -i chr8.pan.og -b chm13.chr8.w5kbps.bed --threads 2 | \
    bedtools sort > chr8.pan.depth.w5kbps.bed

The chm13.chr8.w5kbps.bed file contains 5000 bps interval windows across the chm13 reference chromosome 8. The depth is computed for each of these windows, writing the result in the chr8.pan.depth.w5kbps.bed file, in BED format. -r specifies the path name from which to compute the depth from. -b specifies the BED ranges of which the depths should be calculated of.

Note

It will take a while to obtain the depth over all the windows. You can find the gzipped result in the test folder in the root of the odgi project, in the chr8.pan.depth.w5kbps.bed.gz file. Gunzip the file before using it.

Take a look at the first rows of the chr8.pan.depth.w5kbps.bed file:

head chr8.pan.depth.w5kbps.bed -n 5 | column -t

chm13#chr8  0      5000   60.1014
chm13#chr8  5000   10000  89.5402
chm13#chr8  10000  15000  91.1302
chm13#chr8  15000  20000  90.0506
chm13#chr8  20000  25000  94.0238

The 4-th column indicates the mean depth of each window. For each node within a window, the product between the node depth and its length (in bp) is calculated. The overall total sum is divided by the length of the window (in bp). This results in the mean depth.

Plot the depth¶

Plotting the mean depth distribution:

Mean depth distribution of chromosome 8: Three high depth regions are present. Left: The β-defensin gene cluster. Mid: The centromere. Right: The neo-centromere.

The centromere’s Higher-Order Repeat (HOR) organization¶

The chromosome 8 centromeric HOR array is primarily composed of four distinct HOR types represented by 4, 7, 8 or 11 α-satellite monomer cassettes. Thankfully, Logsdon et al., Nature 2021 provide HOR annotations (you can find them in the test folder in the root of the odgi project, in the chr8_HORarray_organization.colors.bed file), so we can take a closer look at the centromere:

Mean depth of the chromosome 8 centromeric HOR array. Every letter indicates an alpha-satellite monomer in the HOR (so, A,B,C,D,E,F,G,H,I,J,K would indicate an HOR with 11 alpha-satellite monomers). The mean depth drop falls into the hypomethylated and CENP-A-enriched regions, that have the highest consistent entropy in the entire array. This is in concordance with the Logsdon et al., Nature 2021 publication, see the figure below. The drop in the depth may indicate hypervariability between genomes in the transition from methylated to unmethylated DNA, or that the region is not alignable.

../../_images/chr8_HOR.organization.2.png

Overview of the chm13 chromosome 8 D8Z2 α-satellite HOR array. a (top): Monomer arrangements of the HOR. a (bottom): The entropy plot of chromosome 8 reveals that the hypomethylated and CENP-A-enriched regions, that have the highest consistent entropy in the entire array. b: Structure of the α-satellite monomers listed by HOR. c: Frequency plot of the α-satellite monomers in the HOR. Figure taken from Logsdon et al., Nature 2021.