Evidence map›Paper›PMID 32665660›Full record

ArticleNature biotechnology2020

Automated assembly of centromeres from ultra-long error-prone reads.

Andrey V Bzikadze, Pavel A Pevzner

Open access · greenAbstract read
In one paragraph

Article in Nature biotechnology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
15.8field-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

43 citing papers in PubMed, 75 citations in OpenAlex.

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  9. Methods for Chromosome-Scale Haplotype Reconstruction.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  10. Centromere Landscapes Resolved from Hundreds of Human Genomes.Genomics, proteomics & bioinformatics · 2024
    Article
  11. Review
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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

2 authors at 1 institution in 1 country.

Andrey V BzikadzeGraduate Program in Bioinformatics and Systems Biology, University of California San Diego, La Jolla, CA, USA.
Pavel A PevznerDepartment of Computer Science and Engineering, University of California San Diego, La Jolla, CA, USA. ppevzner@ucsd.edu.ORCID http://orcid.org/0000-0002-0418-165X
University of California San Diego · US

Funding

A New Approach to Fragment Assembly in DNA SequencingR01HG002366 · NHGRI · UNIVERSITY OF CALIFORNIA SAN DIEGO · PI PEVZNER, PAVEL A · 2001 to 2003
$2.2M
NHGRI NIH HHS R01 HG002366
6 · The paper itself

Abstract

Centromeric variation has been linked to cancer and infertility, but centromere sequences contain multiple tandem repeats and can only be assembled manually from long error-prone reads. Here we describe the centroFlye algorithm for centromere assembly using long error-prone reads, and apply it to assemble human centromeres on chromosomes 6 and X. Our analyses reveal putative breakpoints in the manual reconstruction of the human X centromere, demonstrate that human X chromosome is partitioned into repeat subfamilies and provide initial insights into centromere evolution. We anticipate that centroFlye could be applied to automatically close remaining multimegabase gaps in the reference human genome.

Indexed as

AutomationCentromereEvolution, MolecularHumansSequence Analysis, DNATandem Repeat Sequences

Identifiers

PMID32665660
PMCPMC10718184
OpenAlexW3042933198

What OpenQuestion holds

Textmetadata
LicenceTDM
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.