Evidence map›Paper›PMID 32469863›Full record

ArticlePLoS computational biology2020

Ranbow: A fast and accurate method for polyploid haplotype reconstruction.

M-Hossein Moeinzadeh, Jun Yang, Evgeny Muzychenko, Giuseppe Gallone, David Heller, Knut Reinert, Stefan Haas, Martin Vingron

Abstract read
In one paragraph

Article in PLoS computational biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
–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

15 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Evolution of Plant Genome Size and Composition.Genomics, proteomics & bioinformatics · 2024
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Recent Advances in Assembly of Complex Plant Genomes.Genomics, proteomics & bioinformatics · 2023
    Review
  10. Article
  11. Article
  12. Article
  13. flopp: Extremely Fast Long-Read Polyploid Haplotype Phasing by Uniform Tree Partitioning.Journal of computational biology : a journal of computational molecular cell biology · 2022
    Article
  14. Article
  15. Article
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

8 authors.

M-Hossein MoeinzadehMax Planck Institute for Molecular Genetics, Berlin, Germany.ORCID 0000-0002-6787-3047
Jun YangMax Planck Institute for Molecular Genetics, Berlin, Germany.ORCID 0000-0002-0371-8814
Evgeny MuzychenkoMax Planck Institute for Molecular Genetics, Berlin, Germany.
Giuseppe GalloneMax Planck Institute for Molecular Genetics, Berlin, Germany.ORCID 0000-0001-6806-7226
David HellerMax Planck Institute for Molecular Genetics, Berlin, Germany.ORCID 0000-0001-8346-9565
Knut ReinertDepartment of Mathematics and Computer Science, Freie Universitat Berlin, Berlin, Germany.ORCID 0000-0003-3078-8129
Stefan HaasMax Planck Institute for Molecular Genetics, Berlin, Germany.
Martin VingronMax Planck Institute for Molecular Genetics, Berlin, Germany.ORCID 0000-0002-1765-4241

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Reconstructing haplotypes from sequencing data is one of the major challenges in genetics. Haplotypes play a crucial role in many analyses, including genome-wide association studies and population genetics. Haplotype reconstruction becomes more difficult for higher numbers of homologous chromosomes, as it is often the case for polyploid plants. This complexity is compounded further by higher heterozygosity, which denotes the frequent presence of variants between haplotypes. We have designed Ranbow, a new tool for haplotype reconstruction of polyploid genome from short read sequencing data. Ranbow integrates all types of small variants in bi- and multi-allelic sites to reconstruct haplotypes. To evaluate Ranbow and currently available competing methods on real data, we have created and released a real gold standard dataset from sweet potato sequencing data. Our evaluations on real and simulated data clearly show Ranbow's superior performance in terms of accuracy, haplotype length, memory usage, and running time. Specifically, Ranbow is one order of magnitude faster than the next best method. The efficiency and accuracy of Ranbow makes whole genome haplotype reconstruction of complex genome with higher ploidy feasible.

Indexed as

HaplotypesPolyploidyAlgorithmsDatasets as TopicHeterozygoteHumans

Identifiers

PMID32469863
PMCPMC7310859

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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.