Evidence map›Paper›PMID 24532781›Full record

ArticleGenetics2014

Exploiting the extraordinary genetic polymorphism of ciona for developmental genetics with whole genome sequencing.

Sarah Abdul-Wajid, Michael T Veeman, Shota Chiba, Thomas L Turner, William C Smith

Open access · bronzeAbstract read
In one paragraph

Article in Genetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Article
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  5. Review
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

5 authors at 1 institution in 1 country.

Sarah Abdul-WajidDepartment of Molecular, Cellular and Developmental Biology, University of California, Santa Barbara, California 93106.
Michael T Veeman
Shota Chiba
Thomas L Turner
William C Smith
University of California, Santa Barbara · US

Funding

Mutational Analysis of Tunicate DevelopmentR01HD038701 · NICHD · UNIVERSITY OF CALIFORNIA SANTA BARBARA · PI SMITH, WILLIAM · 2000 to 2020
$5.8M
Evolutionary Behavioral Genomics of Drosophila CourtshipR01GM098614 · NIGMS · UNIVERSITY OF CALIFORNIA SANTA BARBARA · PI TURNER, THOMAS LEE · 2011 to 2015
$1.4M
NICHD NIH HHS HD038701NICHD NIH HHS R01 HD038701NIGMS NIH HHS GM098614NIGMS NIH HHS R01 GM098614
6 · The paper itself

Abstract

Studies in tunicates such as Ciona have revealed new insights into the evolutionary origins of chordate development. Ciona populations are characterized by high levels of natural genetic variation, between 1 and 5%. This variation has provided abundant material for forward genetic studies. In the current study, we make use of deep sequencing and homozygosity mapping to map spontaneous mutations in outbred populations. With this method we have mapped two spontaneous developmental mutants. In Ciona intestinalis we mapped a short-tail mutation with strong phenotypic similarity to a previously identified mutant in the related species Ciona savignyi. Our bioinformatic approach mapped the mutation to a narrow interval containing a single mutated gene, α-laminin3,4,5, which is the gene previously implicated in C. savignyi. In addition, we mapped a novel genetic mutation disrupting neural tube closure in C. savignyi to a T-type Ca(2+) channel gene. The high efficiency and unprecedented mapping resolution of our study is a powerful advantage for developmental genetics in Ciona, and may find application in other outbred species.

Indexed as

Polymorphism, GeneticAnimalsBase SequenceChromosome MappingCiona intestinalisGenes, DevelopmentalGenetic LociGenomicsHomozygoteMutationNeural TubeSequence Analysis, DNACionagenetic variationmutantwhole-genome sequencing

Identifiers

PMID24532781
PMCPMC4012500
OpenAlexW2116300300

What OpenQuestion holds

Textmetadata
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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.