Evidence map›Paper›PMID 41889883›Full record

ArticlebioRxiv : the preprint server for biology2026

VICAST: An Integrated Toolkit for Viral Genome Annotation Curation and Low-Frequency Variant Analysis in Passage Studies.

Kathie A Mihindukulasuriya, Luis Alberto Chica Cardenas, Scott A Handley

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 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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0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

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

3 authors.

Kathie A MihindukulasuriyaDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.ORCID 0000-0001-9372-3758
Luis Alberto Chica CardenasDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.ORCID 0009-0007-7408-9385
Scott A HandleyDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.ORCID 0000-0002-2143-6570

Funding

A consortium facilitation, coordination, and data management center for the HVPU24HL175772 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI Curtis Huttenhower, Owen R White · 2025 to 2026
$5.9M
NHLBI NIH HHS U24 HL175772
6 · The paper itself

Abstract

Cultured virus passage studies are fundamental to understanding viral evolution, attenuation, and host adaptation, yet analyzing genomic changes across passages requires both accurate functional annotation of viral genomes and sensitive detection of low-frequency variants. Existing tools address these needs separately: automated annotation pipelines such as VADR and VIGOR4 perform well for well-characterized virus families but struggle with poorly-annotated or novel genomes, while variant calling pipelines designed for clinical diagnostics focus on consensus sequences rather than the low-frequency variants (3-50% frequency) that are biologically meaningful in passage studies. Here we present VICAST (Viral Cultured-virus Annotation and SnpEff Toolkit), an integrated software suite that combines semi-automated genome annotation with manual curation checkpoints and low-frequency variant calling optimized for viral populations. VICAST provides four annotation pathways to accommodate diverse genome annotation quality, including polyproteins, unannotated and multi-segmented genomes. It integrates with SnpEff for functional variant annotation and includes a BAM-level read co-occurrence module for haplotype validation. We validated VICAST using publicly available datasets from three virus families representing distinct analytical challenges: SARS-CoV-2 for polyprotein cleavage-aware annotation, Dengue virus 2 for standard flavivirus annotation and low-frequency variant detection, and Influenza A H1N1 for multi-segmented genome handling. Additionally, VICAST's annotation curation workflow has produced validated annotations not available from NCBI, including protein-level annotations for Chikungunya virus (NC_004162.2). These curated annotations have been incorporated into a custom SnpEff database distributed with VICAST, enabling immediate functional variant annotation for Chikungunya without requiring users to build the database from scratch. Benchmark comparisons with VADR demonstrate VICAST's advantages for passage study workflows, including 5.6-8.1 times faster processing and integrated contamination screening. VICAST is freely available at https://github.com/mihinduk/VICAST and distributed as both Docker containers and conda-based installations.

Indexed as

genome annotationpassage studiespolyproteinquasispeciesSnpEfftissue culturevariant callingviral genomics

Identifiers

PMID41889883
PMCPMC13015546

What OpenQuestion holds

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LicenceCC BY
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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.