Evidence map›Paper›PMID 24642969›Full record

ArticlePloS one2014

Development and characterization of simple sequence repeat (SSR) markers based on RNA-sequencing of Medicago sativa and in silico mapping onto the M. truncatula genome.

Zan Wang, Guohui Yu, Binbin Shi, Xuemin Wang, Haiping Qiang, Hongwen Gao

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
9.3field-weighted citation impact, top 2% 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

22 citing papers in PubMed, 62 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Frontiers in plant science · 2022
    Article
  6. Article
  7. Article
  8. Article
  9. Cross-genera amplification ofPhysiology and molecular biology of plants : an international journal of functional plant biology · 2020
    Article
  10. Development of EST-SSR markers forPhysiology and molecular biology of plants : an international journal of functional plant biology · 2020
    Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. RNA-Seq of Guar (Frontiers in plant science · 2017
    Article
  19. Article
  20. Article
4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Zan WangInstitute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing, China.
Guohui YuInstitute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing, China; Department of Grassland Science, College of Animal Science and Technology, Northwest A&F University, Yangling, Shaanxi, China.
Binbin ShiInstitute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing, China.
Xuemin WangInstitute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing, China.
Haiping QiangInstitute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing, China.
Hongwen GaoInstitute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing, China.
Chinese Academy of Agricultural Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sufficient codominant genetic markers are needed for various genetic investigations in alfalfa since the species is an outcrossing autotetraploid. With the newly developed next generation sequencing technology, a large amount of transcribed sequences of alfalfa have been generated and are available for identifying SSR markers by data mining. A total of 54,278 alfalfa non-redundant unigenes were assembled through the Illumina HiSeqTM 2000 sequencing technology. Based on 3,903 unigene sequences, 4,493 SSRs were identified. Tri-nucleotide repeats (56.71%) were the most abundant motif class while AG/CT (21.7%), AGG/CCT (19.8%), AAC/GTT (10.3%), ATC/ATG (8.8%), and ACC/GGT (6.3%) were the subsequent top five nucleotide repeat motifs. Eight hundred and thirty- seven EST-SSR primer pairs were successfully designed. Of these, 527 (63%) primer pairs yielded clear and scored PCR products and 372 (70.6%) exhibited polymorphisms. High transferability was observed for ssp falcata at 99.2% (523) and 71.7% (378) in M. truncatula. In addition, 313 of 527 SSR marker sequences were in silico mapped onto the eight M. truncatula chromosomes. Thirty-six polymorphic SSR primer pairs were used in the genetic relatedness analysis of 30 Chinese alfalfa cultivated accessions generating a total of 199 scored alleles. The mean observed heterozygosity and polymorphic information content were 0.767 and 0.635, respectively. The codominant markers not only enriched the current resources of molecular markers in alfalfa, but also would facilitate targeted investigations in marker-trait association, QTL mapping, and genetic diversity analysis in alfalfa.

Indexed as

Genes, PlantGenome, PlantMicrosatellite RepeatsAllelesChromosome MappingGenetic MarkersHeterozygoteHigh-Throughput Nucleotide SequencingMedicago sativaMedicago truncatulaPloidiesPolymorphism, GeneticQuantitative Trait LociGenetic Markers

Identifiers

PMID24642969
PMCPMC3958398
OpenAlexW2075584191

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.