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Biology subjects

Kamaraj, V.

Publications and source records attributed to Kamaraj, V..

2 recordsLinked to original sources

Unveiling Genomic Complexity: A Framework for Genome Graph Structural Analysis and Optimised Variant Calling Workflows

MotivationGenome graphs represent genetic diversity by highlighting polymorphic regions, but current methods lack the ability to characterize and compare their complex structures effectively. ResultsOur study introduces GViNC: a framework for Genome graph Visualisation, Navigation, and Comparison. GViNC maps genomic coordinates onto genome graph nodes, facilitating subgraph partitioning by regions, which aids in navigating and comparing genetic data. Applied to multiple genome graphs from the 1,000 Genomes Project, we observed that genomic complexity varies by ancestry and chromosomes, with rare variants increasing variability significantly. GViNC identified key regions like HLA and DEFB loci, revealing population-specific heterogeneity linked to essential biological functions. Its versatility and scalability support extensive research on genetic diversity across different cohorts or species. Availability and ImplementationGViNC, automated with Snakemake, is available at https://github.com/IBSE-IITM/GViNC. Contact(K.R.) kraman@iitm.ac.in, (M.N) nmanik@cse.iitm.ac.in, (H.S.) sinha@iitm.ac.in Supplementary informationA supplementary document with tables and figures accompanies this manuscript.

genomics↗

SCI-VCF: A cross-platform application to summarise, compare and design interactive visualisations of the variant call format

As genomics advances swiftly and its applications extend to diverse fields, bioinformatics tools must enable researchers and clinicians to work with genomic data irrespective of their programming expertise. We developed SCI-VCF, a Shiny-based comprehensive analysis utility to summarise, compare, inspect, analyse, and design interactive visualisations of the genetic variants from the variant call format. With an intuitive GUI, SCI-VCF aims to bridge the approachability gap in genomics that arises from the existing predominantly command-line utilities. SCI-VCF is written with R and is freely available at https://github.com/HimanshuLab/SCI-VCF. For installation-free access, users can avail of an online version at https://ibse.shinyapps.io/sci-vcf-online/.

bioinformatics↗