Evidence map›Paper›PMID 24564644›Full record

ArticleBMC bioinformatics2013

Disentangling homeologous contigs in allo-tetraploid assembly: application to durum wheat.

Vincent Ranwez, Yan Holtz, Gautier Sarah, Morgane Ardisson, Sylvain Santoni, Sylvain Glémin, Muriel Tavaud-Pirra, Jacques David

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Article in BMC bioinformatics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Modern Approaches for Transcriptome Analyses in Plants.Advances in experimental medicine and biology · 2021
    Article
  2. Multiple origins of green coloration in frogs mediated by a novel biliverdin-binding serpin.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  3. Article
  4. Article
  5. Epistatic determinism of durum wheat resistance to the wheat spindle streak mosaic virus.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2017
    Article
  6. Article
  7. Article
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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Vincent Ranwez
Yan Holtz
Gautier Sarah
Morgane Ardisson
Sylvain Santoni
Sylvain Glémin
Muriel Tavaud-Pirra
Jacques David

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundUsing Next Generation Sequencing, SNP discovery is relatively easy on diploid species and still hampered in polyploid species by the confusion due to homeology. We develop HomeoSplitter; a fast and effective solution to split original contigs obtained by RNAseq into two homeologous sequences. It uses the differential expression of the two homeologous genes in the RNA. We verify that the new sequences are closer to the diploid progenitors of the allopolyploid species than the original contig. By remapping original reads on these new sequences, we also verify that the number of valuable detected SNPs has significantly increased.

resultsHomeoSplitter is a fast and effective solution to disentangle homeologous sequences based on a maximum likelihood optimization. On a benchmark set of 2,505 clusters containing homologous sequences of urartu, speltoides and durum, HomeoSplitter was efficient to build sequences closer to the diploid references and increased the number of valuable SNPs from 188 out of 1,360 SNPs detected when mapping the reads on the de novo durum assembly to 762 out of 1,620 SNPs when mapping on HomeoSplitter contigs.

conclusionsThe HomeoSplitter program is freely available at http://bioweb.supagro.inra.fr/homeoSplitter/. This work provides a practical solution to the complex problem of disentangling homeologous transcripts in allo-tetraploids, which further allows an improved SNP detection.

Indexed as

Sequence Analysis, DNATetraploidyBase SequenceDiploidyHigh-Throughput Nucleotide SequencingPolymorphism, Single NucleotideTriticum

Identifiers

PMID24564644
PMCPMC3851826

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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.