Exploratory analysis

Synopsis

Visualizing pangenome graphs we can gain insight into the mutual relationship between the embedded genomes and their variation. However, complex, nonlinear graph structures are difficult to present in a convenient number of dimensions. odgi viz offers a binned, linearized 1-Dimensional rendering. It is able to display gigabase scale pangenomes, and several visualization modalities to grasp the complexity in the graphs.

Steps

Build the DRB1-3123 graph

Assuming that your current working directory is the root of the odgi project, to construct an odgi file from the DRB1-3123 dataset in GFA format, execute:

odgi build -g test/DRB1-3123.gfa -o DRB1-3123.og

The command creates a file called DRB1-3123.og, which contains the input graph in odgi format. This graph contains 12 ALT sequences of the HLA-DRB1 gene from the GRCh38 reference genome.

Visualize the DRB1-3123 graph

To visualize the graph, execute:

odgi viz -i DRB1-3123.og -o DRB1-3123.png -x 500

To obtain the following PNG image:

../../_images/DRB1-3123.png

In this 1-Dimensional visualization:

  • The graph nodes are arranged from left to right, forming the pangenome sequence.

  • The colored bars represent the the paths versus the pangenome sequences in a binary matrix.

  • The path names are visualized on the left.

  • The black lines under the paths are the links, which represent the graph topology.

See odgi viz documentation for more information.

Color with respect to the node position

This is a linearized visualization, but the pangenome graphs are not linear when the embedded genomes present structural variation. However, a graph can be optimized for being better visualized in 1-Dimension by sorting its nodes properly (see the Sorting and Layouting tutorial for more information).

To color the bars with respect to the node position in each path, execute:

odgi viz -i DRB1-3123.og -o DRB1-3123.du.png -x 500 -d -u

To obtain the following PNG image:

../../_images/DRB1-3123.du.png

For each path, the brightness goes from light (for the starting position) to black (for the ending position). A linear genome in a well-sorted graph appears with a smooth brightness gradient in this visualization modality. -d changes the color darkness based on the nucleotide position in the path. -u sets the color darkness range from white for the first nucleotide position of a path to black for the last nucleotide position of a path.

Interestingly, the >gi|345525392:5000-18402 path has a brightness gradient which go from right to left. DNA sequence graphs have two strands, with the node implicitly representing both strands. That gradient indicates that the path is reversed with respect to the pangenome sequence.

Color with respect to the node strandedness

To color the bars with respect to the strandedness that each node has in each path, execute:

odgi viz -i DRB1-3123.og -o DRB1-3123.z.png -x 500 -z

to obtain the following PNG image:

../../_images/DRB1-3123.z.png

-z changes the color palette to respect the node strandedness. Black is forward, red is reverse. The red bar in a path indicates that that region is inverted in that path with respect to the pangenome sequence.

Build the Lipoprotein A graph

Assuming that your current working directory is the root of the odgi project, to construct an odgi file from the LPA dataset in GFA format, execute:

odgi build -g test/LPA.gfa -o LPA.og

The command creates a file called LPA.og, which contains the input graph in odgi format. This graph contains 13 contigs from 7 haploid human genome assemblies from 6 individuals plus the chm13 cell line. The contigs cover the Lipoprotein A (LPA) locus, which encodes the Apo(a) protein.

Visualize the LPA graph

To visualize the graph, execute:

odgi viz -i LPA.og -o LPA.b.png -x 500 -b

To obtain the following PNG image:

../../_images/LPA.b.png

Color with respect to the node depth in a path

Eukaryotic genomes are characterized by repetitive sequences. These sequences can lead to complex regions in the pangenome graphs. To identify them, we can analyze the depth in the graph. Here we define node depth in a path as the number of times the node is crossed by a path.

To color the bars with respect to the mean depth, execute:

odgi viz -i LPA.og -o LPA.bm.png -x 500 -bm

To obtain the following PNG image:

../../_images/LPA.bm.png

Low depth regions are black, while high depth regions are colored green. Apo(a) proteins vary in size due to a size polymorphism, the KIV-2 variable numbers of tandem repeats (VNTRs). The VNTR region in the LPA pangenome presents high depth, that becomes evident as a light green stripe in the image. -b explicitly forces odgi viz to bin the graph before visualizing it. -m changes the color palette to display the mean depth per bin as a shade of green.

Visualize a particular region

To obtain the coordinates of the VNTRs, execute:

odgi depth -i LPA.og -r chm13__LPA__tig00000001| \
    bedtools makewindows -b /dev/stdin -w 5000 > chm13__LPA__tig00000001.w5kbps.bed

odgi depth -i LPA.og -b chm13__LPA__tig00000001.w5kbps.bed | \
    bedtools sort > chm13__LPA__tig00000001.depth.w5kbps.bed

awk -F"\t" '$4 > 20.0' chm13__LPA__tig00000001.depth.w5kbps.bed | \
    bedtools merge

chm13__LPA__tig00000001 140000  275000

The chm13__LPA__tig00000001.w5kbps.bed file contains 5000 bp interval windows across the chm13__LPA__tig00000001 contig. The depth is computed for each of these windows, writing the result in the chm13__LPA__tig00000001.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.

To visualize the identified region, execute:

odgi viz -i LPA.og -o LPA.bm.VNTRs.png -x 500 -bm -r chm13__LPA__tig00000001:140000-275000

To obtain the following PNG image:

../../_images/LPA.bm.VNTRs.png