Evidence map›Paper›PMID 37843753›Full record

ArticleTransgenic research2023

A timely, user-friendly, and flexible marker-assisted speed congenics method.

Anne-Sophie Van Laere, Audrey Tromme, Laetitia Delaval, Frédéric Farnir, Joël Blomet, Daniel Desmecht

Abstract read
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In one paragraph

Article in Transgenic research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Anne-Sophie Van LaereDepartment of Pathology, FARAH, Faculty of Veterinary Medicine, University of Liege, Liège, Belgium.
Audrey TrommeDepartment of Pathology, FARAH, Faculty of Veterinary Medicine, University of Liege, Liège, Belgium.
Laetitia DelavalDepartment of Pathology, FARAH, Faculty of Veterinary Medicine, University of Liege, Liège, Belgium.
Frédéric FarnirBiostatistics and Bioinformatics, FARAH, Faculty of Veterinary Medicine, University of Liege, Liège, Belgium.
Joël BlometLaboratoires Prevor, Moulin de Verville, 95670, Valmondois, France.
Daniel DesmechtDepartment of Pathology, FARAH, Faculty of Veterinary Medicine, University of Liege, Liège, Belgium. Daniel.Desmecht@Uliege.be.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mice are the most widely used mammalian animal model worldwide. Their use presents many advantages, including our ability to manipulate their genome. Unfortunately, transgenic mice often need to be introgressed to transfer the transgene of interest in a specific mouse line. This time-consuming process can be shortened using the speed congenics technique. However, the need for a panel of informative markers to evaluate the proportion of donor and receiver genomes in different individuals produced at each generation hinders the utilisation of speed congenics. In this study, we present 255 microsatellites and 10 RFLPs which can be used in 18 marker panels, allowing the easy and fast introgression of genes of interest from three mouse lines commonly used for transgenesis (C57BL/6, 129/Sv and FVB) to six mouse lines relevant for biomedical research (BALB/c, C3H, DBA/1, DBA/2, SJL and SWR/J). In addition, our markers analysis confirmed a recently described lack of isogeny in well-established inbred mouse lines available from commercial breeders.

Indexed as

GenomeMammalsAnimalsMiceMice, Inbred C3HMice, Inbred C57BLMice, Inbred DBAMice, TransgenicIntrogressionIsogenyMicrosatelliteMouseSpeed congenics

Identifiers

What OpenQuestion holds

Textmetadata
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.