Evidence map›Paper›PMID 35686922›Full record

ArticleG3 (Bethesda, Md.)2022

Assembly of complete diploid-phased chromosomes from draft genome sequences.

Andrea Minio, Noé Cochetel, Amanda M Vondras, Mélanie Massonnet, Dario Cantu

Abstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed.

  1. Article
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  7. Review
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  10. The genome ofHorticulture research · 2025
    Article
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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

5 authors.

Andrea MinioDepartment of Viticulture and Enology, University of California Davis, Davis, CA 95616, USA.ORCID 0000-0003-2643-9209
Noé CochetelDepartment of Viticulture and Enology, University of California Davis, Davis, CA 95616, USA.ORCID 0000-0003-3395-9536
Amanda M VondrasDepartment of Viticulture and Enology, University of California Davis, Davis, CA 95616, USA.ORCID 0000-0001-8882-3914
Mélanie MassonnetDepartment of Viticulture and Enology, University of California Davis, Davis, CA 95616, USA.ORCID 0000-0003-0993-9148
Dario CantuDepartment of Viticulture and Enology, University of California Davis, Davis, CA 95616, USA.ORCID 0000-0002-4858-1508

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

De novo genome assembly is essential for genomic research. High-quality genomes assembled into phased pseudomolecules are challenging to produce and often contain assembly errors because of repeats, heterozygosity, or the chosen assembly strategy. Although algorithms that produce partially phased assemblies exist, haploid draft assemblies that may lack biological information remain favored because they are easier to generate and use. We developed HaploSync, a suite of tools that produces fully phased, chromosome-scale diploid genome assemblies, and performs extensive quality control to limit assembly artifacts. HaploSync scaffolds sequences from a draft diploid assembly into phased pseudomolecules guided by a genetic map and/or the genome of a closely related species. HaploSync generates a report that visualizes the relationships between current and legacy sequences, for both haplotypes, and displays their gene and marker content. This quality control helps the user identify misassemblies and guides Haplosync's correction of scaffolding errors. Finally, HaploSync fills assembly gaps with unplaced sequences and resolves collapsed homozygous regions. In a series of plant, fungal, and animal kingdom case studies, we demonstrate that HaploSync efficiently increases the assembly contiguity of phased chromosomes, improves completeness by filling gaps, corrects scaffolding, and correctly phases highly heterozygous, complex regions.

Indexed as

DiploidyGenomeAnimalsChromosomesGenomicsHaplotypesSequence Analysis, DNAassembly error correctionchromosome anchoringdiploid genomeshaplotype phasinghybrid genome assembly

Identifiers

PMID35686922
PMCPMC9339290

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.