[HTML][HTML] Visualizing genomic information across chromosomes with PhenoGram

D Wolfe, S Dudek, MD Ritchie, SA Pendergrass - BioData mining, 2013 - Springer
D Wolfe, S Dudek, MD Ritchie, SA Pendergrass
BioData mining, 2013Springer
Background With the abundance of information and analysis results being collected for
genetic loci, user-friendly and flexible data visualization approaches can inform and improve
the analysis and dissemination of these data. A chromosomal ideogram is an idealized
graphic representation of chromosomes. Ideograms can be combined with overlaid points,
lines, and/or shapes, to provide summary information from studies of various kinds, such as
genome-wide association studies or phenome-wide association studies, coupled with …
Background
With the abundance of information and analysis results being collected for genetic loci, user-friendly and flexible data visualization approaches can inform and improve the analysis and dissemination of these data. A chromosomal ideogram is an idealized graphic representation of chromosomes. Ideograms can be combined with overlaid points, lines, and/or shapes, to provide summary information from studies of various kinds, such as genome-wide association studies or phenome-wide association studies, coupled with genomic location information. To facilitate visualizing varied data in multiple ways using ideograms, we have developed a flexible software tool called PhenoGram which exists as a web-based tool and also a command-line program.
Results
With PhenoGram researchers can create chomosomal ideograms annotated with lines in color at specific base-pair locations, or colored base-pair to base-pair regions, with or without other annotation. PhenoGram allows for annotation of chromosomal locations and/or regions with shapes in different colors, gene identifiers, or other text. PhenoGram also allows for creation of plots showing expanded chromosomal locations, providing a way to show results for specific chromosomal regions in greater detail. We have now used PhenoGram to produce a variety of different plots, and provide these as examples herein. These plots include visualization of the genomic coverage of SNPs from a genotyping array, highlighting the chromosomal coverage of imputed SNPs, copy-number variation region coverage, as well as plots similar to the NHGRI GWA Catalog of genome-wide association results.
Conclusions
PhenoGram is a versatile, user-friendly software tool fostering the exploration and sharing of genomic information. Through visualization of data, researchers can both explore and share complex results, facilitating a greater understanding of these data.
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