Evidence map›Paper›PMID 33390838›Full record

ReviewInternational journal of biological sciences2021

Genome-to-phenome research in rats: progress and perspectives.

Amy L Zinski, Shane Carrion, Jennifer J Michal, Maria A Gartstein, Raymond M Quock, Jon F Davis, Zhihua Jiang

Abstract readReview
In one paragraph

Review in International journal of biological sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–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

4 citing papers in PubMed.

  1. RNA variation as the driver of genomic efficiency and phenotypic complexity.International journal of biological sciences · 2026
    Review
  2. Rat models of musculoskeletal lysosomal storage disorders and their role in pre-clinical evaluation of gene therapy approaches.Mammalian genome : official journal of the International Mammalian Genome Society · 2025
    Review
  3. Review
  4. 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

7 authors.

Amy L ZinskiDepartment of Animal Sciences, Washington State University, Pullman, WA 99164-7620.
Shane CarrionDepartment of Animal Sciences, Washington State University, Pullman, WA 99164-7620.
Jennifer J MichalDepartment of Animal Sciences, Washington State University, Pullman, WA 99164-7620.
Maria A GartsteinDepartment of Psychology, Washington State University, Pullman, WA 99164-4820.
Raymond M QuockDepartment of Psychology, Washington State University, Pullman, WA 99164-4820.
Jon F DavisDepartment of Integrative Physiology and Neuroscience, Washington State University, Pullman, WA 99164-7620.
Zhihua JiangDepartment of Animal Sciences, Washington State University, Pullman, WA 99164-7620.

Funding

Standardized Next Generation Transcriptome Profiling Tools for X. TropicalisR21HD076845 · NICHD · WASHINGTON STATE UNIVERSITY · PI JIANG, ZHIHUA · 2013 to 2014
$396k
NICHD NIH HHS R21 HD076845
6 · The paper itself

Abstract

Because of their relatively short lifespan (<4 years), rats have become the second most used model organism to study health and diseases in humans who may live for up to 120 years. First-, second- and third-generation sequencing technologies and platforms have produced increasingly greater sequencing depth and accurate reads, leading to significant advancements in the rat genome assembly during the last 20 years. In fact, whole genome sequencing (WGS) of 47 strains have been completed. This has led to the discovery of genome variants in rats, which have been widely used to detect quantitative trait loci underlying complex phenotypes based on gene, haplotype, and sweep association analyses. DNA variants can also reveal strain, chromosome and gene functional evolutions. In parallel, phenome programs have advanced significantly in rats during the last 15 years and more than 10 databases host genome and/or phenome information. In order to discover the bridges between genome and phenome, systems genetics and integrative genomics approaches have been developed. On the other hand, multiple level information transfers from genome to phenome are executed by differential usage of alternative transcriptional start (ATS) and polyadenylation (APA) sites per gene. We used our own experiments to demonstrate how alternative transcriptome analysis can lead to enrichment of phenome-related causal pathways in rats. Development of advanced genome-to-phenome assays will certainly enhance rats as models for human biomedical research.

Indexed as

Disease Models, AnimalPhenotypeAnimalsRatsWhole Genome SequencingAlternative transcriptomesGenetic variationGenome sequencingGenome-to-phenomePhenome collectionRat

Identifiers

PMID33390838
PMCPMC7757052

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.