Evidence map›Paper›PMID 42894138›Full record

ArticleBMC bioinformatics2026

Fast and inexpensive visualization of genome collection at scale.

Sujatha Kotte, Naina Tiwari, Kavya Vaddadi, Vangala Govindakrishnan Saipradeep, Thomas Joseph, Aditya Rao, Rajgopal Srinivasan, Naveen Sivadasan

Abstract read
In one paragraph

Article in BMC bioinformatics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Sujatha KotteTCS Research, Tata Consultancy Services (TCS) Ltd, Hyderabad, India.
Naina TiwariTCS Research, Tata Consultancy Services (TCS) Ltd, Hyderabad, India.
Kavya VaddadiTCS Research, Tata Consultancy Services (TCS) Ltd, Hyderabad, India.
Vangala Govindakrishnan SaipradeepTCS Research, Tata Consultancy Services (TCS) Ltd, Hyderabad, India. saipradeep.v@tcs.com.
Thomas JosephTCS Research, Tata Consultancy Services (TCS) Ltd, Hyderabad, India.
Aditya RaoTCS Research, Tata Consultancy Services (TCS) Ltd, Hyderabad, India.
Rajgopal SrinivasanTCS Research, Tata Consultancy Services (TCS) Ltd, Hyderabad, India.
Naveen SivadasanTCS Research, Tata Consultancy Services (TCS) Ltd, Hyderabad, India. naveen.sivadasan@tcs.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInvestigating genetic progression and lineage using sequence data is a fundamental focus within the realm of viral genome research. Given the substantial increase in publicly accessible genome sequences, tools designed for extensive data analytics, particularly insightful visualizations play an important role in elucidating the spatio-temporal evolution as well as the diversity of viral lineages. Existing genome data analysis methods frequently rely on multiple sequence alignment (MSA) and phylogeny computations, making integration of new sequences computationally expensive. Such methods are often metadata agnostic and typically utilize a global distance metric between candidate sequences. We present BOVIZ, a fast and inexpensive method for rich visualization of large-scale genome collections. BOVIZ leverages variant-level features from candidate sequences and employs a novel Bag-Of-Variants (BOV) method that transforms high-dimensional variant feature vectors into a 2D-space, effectively capturing sequence (dis)similarities. BOVIZ circumvents the need for expensive MSA and phylogeny analyses, enabling efficient integration of novel sequences and faster visualization of large-scale sequences on a standard desktop. Furthermore, BOVIZ supports a variety of filters, including metadata filters and selection of genomic regions of interest for effectively capturing localized similarities and dissimilarities on-the-fly. We perform extensive benchmarking of BOVIZ with state-of-the-art visualization methods using the SARS-CoV-2 viral genome dataset.

resultsBOVIZ consistently outperformed these methods in capturing inter-sequence similarity and diversity, offering superior visualization of spatio-temporal and clade-level evolution. It is able to effectively distinguish SARS-CoV-2 lineages into distinct clusters, visualize the evolution of specific sublineages like Omicron and their variant patterns, as well as visualize potential sub-cluster within the SARS-CoV-2 Delta variant.

conclusionBOVIZ is an effective visualization tool for genome surveillance, complementing resource-intensive deep analytics by providing key insights about the underlying genome landscape in a fast and scalable manner.

Indexed as

Genome, ViralGenomicsSARS-CoV-2SoftwareCOVID-19PhylogenySequence AlignmentBOVIZData visualizationGenome atlasLow dimensional embeddingSARS-CoV-2

Identifiers

PMID42894138
PMCPMC13679107

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.