Evidence map›Paper›PMID 41256564›Full record

ArticlebioRxiv : the preprint server for biology2025

Finishing a complete giraffe genome from telomere to telomere with Verkko-Fillet.

Juhyun Kim, Benjamin D Rosen, Sarah E Fumagalli, Kristen L Kuhn, Amy Long, Jeffrey J Schoenebeck, Heather Schwartz, Lan Wu-Cavener, Aleksey V Zimin, Douglas R Cavener and 4 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

5 · Who and what money

Authors and funding

14 authors.

Juhyun KimCenter for Genomics and Data Science Research, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.ORCID 0000-0002-0321-9388
Benjamin D RosenAnimal Genomics and Improvement Laboratory, USDA ARS, Beltsville, MD, USA.ORCID 0000-0001-9395-8346
Sarah E FumagalliAnimal Genomics and Improvement Laboratory, USDA ARS, Beltsville, MD, USA.ORCID 0000-0003-2469-4476
Kristen L KuhnMeat Animal Research Center, USDA-ARS, Clay Center, NE, USA.ORCID 0009-0009-9498-8788
Amy LongCincinnati Zoo and Botanical Garden, Cincinnati, OH, USA.
Jeffrey J SchoenebeckCenter for Genomics and Data Science Research, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.ORCID 0000-0003-4964-2138
Heather SchwartzNashville Zoo, Nashville, TN, USA.
Lan Wu-CavenerDepartment of Biology, Pennsylvania State University, University Park, PA, USA.ORCID 0009-0006-6662-9938
Aleksey V ZiminDepartment of Biomedical Engineering, Johns Hopkins University, Baltimore, MD, USA.ORCID 0000-0001-5091-3092
Douglas R CavenerDepartment of Biology, Pennsylvania State University, University Park, PA, USA.ORCID 0000-0002-1558-7137
Timothy P L SmithMeat Animal Research Center, USDA-ARS, Clay Center, NE, USA.ORCID 0000-0003-1611-6828
Adam M PhillippyCenter for Genomics and Data Science Research, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.ORCID 0000-0003-2983-8934
Sergey KorenCenter for Genomics and Data Science Research, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.ORCID 0000-0002-1472-8962
Arang RhieCenter for Genomics and Data Science Research, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.ORCID 0000-0002-9809-8127

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High-quality genome assemblies are essential for understanding speciation, evolution, and for building reference genomes and pan-genomes. Despite major advances in long-read sequencing technologies and graph-based assembly algorithms, current assemblies often remain incomplete and require refinement, including correction of haplotype switching and resolution of gaps, particularly within repetitive regions such as ribosomal DNA clusters and recent segmental duplications. These limitations largely stem from challenges in graph curation and are not adequately addressed by conventional polishing methods, which focus primarily on nucleotide-level corrections. To overcome these issues, we developed Verkko-Fillet, a Python-based interactive framework for genome graph inspection, editing, and curation that also provides step-by-step guidelines for downstream polishing. Verkko-Fillet takes as input Verkko output files, including the assembly graph, haplotype paths, Hi-C contacts, and additional ONT reads or alternative assemblies aligned to the graph, and offers tools for visualizing, modifying, and exporting curated assembly graphs. It enables users to track changes, resolve complex structural features, fill gaps, and enhance assembly quality beyond conventional polishing. As a case study, we applied Verkko-Fillet to the giraffe genome (

Identifiers

PMID41256564
PMCPMC12621783

What OpenQuestion holds

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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.