Evidence map›Paper›PMID 26530422›Full record

ArticleG3 (Bethesda, Md.)2015

Target Enrichment Improves Mapping of Complex Traits by Deep Sequencing.

Jianjun Guo, Jue Fan, Bernard A Hauser, Seung Y Rhee

Open access · goldAbstract read
In one paragraph

Article in G3 (Bethesda, Md.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.2field-weighted citation impact, top 11% 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

8 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. International journal of molecular sciences · 2025
    Article
  3. Article
  4. Article
  5. Review
  6. Mapping QTLs for 15 morpho-metric traits inPhysiology and molecular biology of plants : an international journal of functional plant biology · 2020
    Article
  7. Article
  8. 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

4 authors at 2 institutions in 1 country.

Jianjun GuoDepartment of Plant Biology, Carnegie Institution for Science, Stanford, California 94305.
Jue FanDepartment of Plant Biology, Carnegie Institution for Science, Stanford, California 94305.
Bernard A HauserDepartment of Biology, Plant Molecular and Cellular Biology Program, University of Florida, Gainesville, Florida 32611.
Seung Y RheeDepartment of Plant Biology, Carnegie Institution for Science, Stanford, California 94305 srhee@carnegiescience.edu.
Department of Plant Biology · USUniversity of Florida · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Complex traits such as crop performance and human diseases are controlled by multiple genetic loci, many of which have small effects and often go undetected by traditional quantitative trait locus (QTL) mapping. Recently, bulked segregant analysis with large F2 pools and genome-level markers (named extreme-QTL or X-QTL mapping) has been used to identify many QTL. To estimate parameters impacting QTL detection for X-QTL mapping, we simulated the effects of population size, marker density, and sequencing depth of markers on QTL detectability for traits with differing heritabilities. These simulations indicate that a high (>90%) chance of detecting QTL with at least 5% effect requires 5000× sequencing depth for a trait with heritability of 0.4-0.7. For most eukaryotic organisms, whole-genome sequencing at this depth is not economically feasible. Therefore, we tested and confirmed the feasibility of applying deep sequencing of target-enriched markers for X-QTL mapping. We used two traits in Arabidopsis thaliana with different heritabilities: seed size (H(2) = 0.61) and seedling greening in response to salt (H(2) = 0.94). We used a modified G test to identify QTL regions and developed a model-based statistical framework to resolve individual peaks by incorporating recombination rates. Multiple QTL were identified for both traits, including previously undiscovered QTL. We call our method target-enriched X-QTL (TEX-QTL) mapping; this mapping approach is not limited by the genome size or the availability of recombinant inbred populations and should be applicable to many organisms and traits.

Indexed as

Chromosome MappingHigh-Throughput Nucleotide SequencingQuantitative Trait, HeritableQuantitative Trait LociAlgorithmsArabidopsisGenetic MarkersInheritance PatternsModels, GeneticPhenotypePolymorphism, Single NucleotideROC CurveSalt ToleranceSeedsGenetic MarkersArabidopsis thalianabulked segregant analysissalt toleranceseed sizetarget-enriched extreme quantitative trait locus mapping

Identifiers

PMID26530422
PMCPMC4704726
OpenAlexW2264832204

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.