Evidence map›Paper›PMID 36453992›Full record

ArticleNucleic acids research2022

Pushing the limits of HiFi assemblies reveals centromere diversity between two Arabidopsis thaliana genomes.

Fernando A Rabanal, Maike Gräff, Christa Lanz, Katrin Fritschi, Victor Llaca, Michelle Lang, Pablo Carbonell-Bejerano, Ian Henderson, Detlef Weigel

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
21.0field-weighted citation impact, top 1% of its field
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

31 citing papers in PubMed, 73 citations in OpenAlex.

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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

9 authors at 3 institutions in 3 countries.

Fernando A RabanalDepartment of Molecular Biology, Max Planck Institute for Biology Tübingen, 72076 Tübingen, Germany.ORCID 0000-0003-1538-9752
Maike GräffDepartment of Molecular Biology, Max Planck Institute for Biology Tübingen, 72076 Tübingen, Germany.
Christa LanzDepartment of Molecular Biology, Max Planck Institute for Biology Tübingen, 72076 Tübingen, Germany.
Katrin FritschiDepartment of Molecular Biology, Max Planck Institute for Biology Tübingen, 72076 Tübingen, Germany.ORCID 0000-0001-8308-7946
Victor LlacaGenomics Technologies, Corteva Agriscience, Johnston, IA 50131, USA.
Michelle LangGenomics Technologies, Corteva Agriscience, Johnston, IA 50131, USA.
Pablo Carbonell-BejeranoDepartment of Molecular Biology, Max Planck Institute for Biology Tübingen, 72076 Tübingen, Germany.
Ian HendersonDepartment of Plant Sciences, University of Cambridge, Cambridge, CB2 3EA, UK.ORCID 0000-0001-5066-1489
Detlef WeigelDepartment of Molecular Biology, Max Planck Institute for Biology Tübingen, 72076 Tübingen, Germany.ORCID 0000-0002-2114-7963
Max Planck Institute for Biology · DECorteva (United States) · USUniversity of Cambridge · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although long-read sequencing can often enable chromosome-level reconstruction of genomes, it is still unclear how one can routinely obtain gapless assemblies. In the model plant Arabidopsis thaliana, other than the reference accession Col-0, all other accessions de novo assembled with long-reads until now have used PacBio continuous long reads (CLR). Although these assemblies sometimes achieved chromosome-arm level contigs, they inevitably broke near the centromeres, excluding megabases of DNA from analysis in pan-genome projects. Since PacBio high-fidelity (HiFi) reads circumvent the high error rate of CLR technologies, albeit at the expense of read length, we compared a CLR assembly of accession Eyach15-2 to HiFi assemblies of the same sample. The use of five different assemblers starting from subsampled data allowed us to evaluate the impact of coverage and read length. We found that centromeres and rDNA clusters are responsible for 71% of contig breaks in the CLR scaffolds, while relatively short stretches of GA/TC repeats are at the core of >85% of the unfilled gaps in our best HiFi assemblies. Since the HiFi technology consistently enabled us to reconstruct gapless centromeres and 5S rDNA clusters, we demonstrate the value of the approach by comparing these previously inaccessible regions of the genome between the Eyach15-2 accession and the reference accession Col-0.

Indexed as

ArabidopsisCentromereDNA, RibosomalHigh-Throughput Nucleotide SequencingSequence Analysis, DNADNA, Ribosomal

Identifiers

PMID36453992
PMCPMC9757041
OpenAlexW4310568221

What OpenQuestion holds

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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.