Evidence map›Paper›PMID 36330812›Full record

ArticleHypertension (Dallas, Tex. : 1979)2023

The Assembled Genome of the Stroke-Prone Spontaneously Hypertensive Rat.

Theodore S Kalbfleisch, Nahla A Hussien AbouEl Ela, Kai Li, Wesley A Brashear, Kelli J Kochan, Andrew E Hillhouse, Yaming Zhu, Isha S Dhande, Eric J Kline, Elizabeth A Hudson and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Hypertension (Dallas, Tex. : 1979), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

13 citing papers in PubMed, 13 citations in OpenAlex.

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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

14 authors at 6 institutions in 1 country.

Theodore S KalbfleischDepartment of Veterinary Science, College of Agriculture, Food, and Environment, University of Kentucky, Lexington, KY (T.S.K., N.A.H., K.L.).ORCID 0000-0002-2370-8189
Nahla A Hussien AbouEl ElaDepartment of Veterinary Science, College of Agriculture, Food, and Environment, University of Kentucky, Lexington, KY (T.S.K., N.A.H., K.L.).ORCID 0000-0002-0408-864X
Kai LiDepartment of Veterinary Science, College of Agriculture, Food, and Environment, University of Kentucky, Lexington, KY (T.S.K., N.A.H., K.L.).
Wesley A BrashearTexas A&M Institute for Genome Sciences and Society, Texas A&M University, College Station, TX (W.A.B., K.J.K., A.E.H.).
Kelli J KochanTexas A&M Institute for Genome Sciences and Society, Texas A&M University, College Station, TX (W.A.B., K.J.K., A.E.H.).ORCID 0000-0001-8124-8283
Andrew E HillhouseTexas A&M Institute for Genome Sciences and Society, Texas A&M University, College Station, TX (W.A.B., K.J.K., A.E.H.).ORCID 0000-0003-4874-7077
Yaming ZhuCenter for Human Genetics, Brown Foundation Institute of Molecular Medicine, University of Texas McGovern School of Medicine, Houston, TX (Y.Z., I.S.D., P.A.D.).
Isha S DhandeCenter for Human Genetics, Brown Foundation Institute of Molecular Medicine, University of Texas McGovern School of Medicine, Houston, TX (Y.Z., I.S.D., P.A.D.).
Eric J KlineDepartment of Biochemistry and Molecular Genetics, University of Louisville, Louisville, KY (E.J.K., E.A.H, M.L.S.).ORCID 0000-0002-4847-4649
Elizabeth A HudsonDepartment of Biochemistry and Molecular Genetics, University of Louisville, Louisville, KY (E.J.K., E.A.H, M.L.S.).
Terence D MurphyNational Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, MD (T.D.M., F.T.-N.).
Françoise Thibaud-NissenNational Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, MD (T.D.M., F.T.-N.).ORCID 0000-0003-4957-7807
Melissa L Smith *Department of Biochemistry and Molecular Genetics, University of Louisville, Louisville, KY (E.J.K., E.A.H, M.L.S.).ORCID 0000-0001-7151-3207
Peter A Doris *Center for Human Genetics, Brown Foundation Institute of Molecular Medicine, University of Texas McGovern School of Medicine, Houston, TX (Y.Z., I.S.D., P.A.D.).ORCID 0000-0002-0565-7939
Texas A&M University · USUniversity of Kentucky · USUniversity of Louisville · USBrown Foundation · USNational Center for Biotechnology Information · USNational Institutes of Health · US

Funding

National Biomedical Information ServicesZIHLM200888 · NLM · NATIONAL LIBRARY OF MEDICINE · PI PALTOO, DINA · 2009 to 2025
$5200.7M
Hypertensive Renal InjuryR01DK081866 · NIDDK · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI DORIS, PETER A · 2009 to 2017
$2.9M
Long-read assembly and annotation of rat genomes that are important models of complex genetic diseaseR01HG011252 · NHGRI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI DORIS, PETER A, KALBFLEISCH, THEODORE · 2021 to 2025
$2.0M
NHGRI NIH HHS R01 HG011252NIDDK NIH HHS R01 DK081866
6 · The paper itself

Abstract

backgroundWe report the creation and evaluation of a de novo assembly of the genome of the spontaneously hypertensive rat, the most widely used model of human cardiovascular disease.

methodsThe genome is assembled from long read sequencing (PacBio HiFi and continuous long read data [CLR]) and scaffolded with long-range structural information obtained from Bionano optical maps and proximity ligation sequencing proximity analysis of the genome. The genome assembly was polished with Illumina short reads. Completeness of the assembly was investigated using Benchmarking Universal Single Copy Orthologs analysis. The genome assembly was also evaluated with the rat reference gene set, using NCBI automated protocols. We also generated orthogonal single molecule transcript sequence reads (Iso-Seq) from 8 tissues and used them to validate the coding assembly, to annotate the assembly with RNA transcripts representing unique full length transcript isoforms for each gene and to determine whether divergences between RefSeq sequences and the assembly were attributable to assembly errors or polymorphisms.

resultsThe assembly analysis indicates that this assembly is comparable in contiguity and completeness to the current rat reference assembly, while the use of HiFi sequencing yields an assembly that is more correct at the single base level. Synteny analysis was performed to uncover the extent of synteny and the presence and distribution of chromosomal rearrangements between the reference and this assembly.

conclusionThe resulting genome assembly is reference quality and captures significant structural variation.

Indexed as

StrokeAnimalsHumansRatsRats, Inbred SHRcardiovascular diseasesgenomicsspontaneously hypertensive ratsyntenywhole genome sequencing

Identifiers

PMID36330812
PMCPMC9814308
OpenAlexW4308180704

What OpenQuestion holds

Textmetadata
LicenceTDM
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.