Candidate Gene Discovery for Dog Cryptorchidism

Author(s):  
Xia Zhao ◽  
Kim Glenn ◽  
Zhiqiang Du ◽  
Max F. Rothschild
2010 ◽  
Vol 3 (1) ◽  
Author(s):  
M. A. Saghai Maroof ◽  
Dominic M. Tucker ◽  
Jeffrey A. Skoneczka ◽  
Brian C. Bowman ◽  
Sucheta Tripathy ◽  
...  

2020 ◽  
Vol 21 (22) ◽  
pp. 8757
Author(s):  
Iris B. A. W. te Paske ◽  
Marjolijn J. L. Ligtenberg ◽  
Nicoline Hoogerbrugge ◽  
Richarda M. de Voer

To discover novel high-penetrant risk loci for hereditary colorectal cancer (hCRC) and polyposis syndromes many whole-exome and whole-genome sequencing (WES/WGS) studies have been performed. Remarkably, these studies resulted in only a few novel high-penetrant risk genes. Given this observation, the possibility and strategy to identify high-penetrant risk genes for hCRC and polyposis needs reconsideration. Therefore, we reviewed the study design of WES/WGS-based hCRC and polyposis gene discovery studies (n = 37) and provide recommendations to optimize discovery and validation strategies. The group of genetically unresolved patients is phenotypically heterogeneous, and likely composed of distinct molecular subtypes. This knowledge advocates for the screening of a homogeneous, stringently preselected discovery cohort and obtaining multi-level evidence for variant pathogenicity. This evidence can be collected by characterizing the molecular landscape of tumors from individuals with the same affected gene or by functional validation in cell-based models. Together, the combined approach of a phenotype-driven, tumor-based candidate gene search might elucidate the potential contribution of novel genetic predispositions in genetically unresolved hCRC and polyposis.


2018 ◽  
Vol 16 (11) ◽  
pp. 1954-1967 ◽  
Author(s):  
Gaurav Agarwal ◽  
Josh Clevenger ◽  
Manish K. Pandey ◽  
Hui Wang ◽  
Yaduru Shasidhar ◽  
...  

2016 ◽  
Vol 11 ◽  
pp. 18-26 ◽  
Author(s):  
Keywan Hassani-Pak ◽  
Martin Castellote ◽  
Maria Esch ◽  
Matthew Hindle ◽  
Artem Lysenko ◽  
...  

2005 ◽  
Vol 96 (6) ◽  
pp. 605-606 ◽  
Author(s):  
Raimond L. Winslow ◽  
Zhong Gao

Cell Reports ◽  
2015 ◽  
Vol 10 (2) ◽  
pp. 148-161 ◽  
Author(s):  
Anas M. Alazami ◽  
Nisha Patel ◽  
Hanan E. Shamseldin ◽  
Shamsa Anazi ◽  
Mohammed S. Al-Dosari ◽  
...  

2021 ◽  
Author(s):  
Mingjiu Li ◽  
Ganggang Guo ◽  
Hélène Pidon ◽  
Michael Melzer ◽  
Alberto R. Prina ◽  
...  

AbstractImplementation of next-generation sequencing in forward genetic screens greatly accelerated gene discovery in species with larger genomes, including many crop plants. In barley, extensive mutant collections are available, however, the causative mutations for many of the genes remains largely unknown. Here we demonstrate how a combination of low-resolution genetic mapping, whole-genome resequencing and comparative functional analyses provides a promising path towards candidate identification of genes involved in plastid biology and / or photosynthesis, even if genes are located in recombination poor regions of the genome. As a proof of concept, we simulated the prediction of a candidate gene for the recently cloned variegation mutant albostrians (HvAST / HvCMF7) and adopted the approach for suggesting HvClpC1 as candidate gene for the yellow-green variegation mutant luteostrians.Author SummaryForward genetics is an approach of identifying a causal gene for a mutant phenotype and has proven to be a powerful tool for dissecting the genetic control of biological processes in many species. A large number of barley mutants was generated in the 1940s to 1970s when mutation breeding programs flourished. Genetic dissection of the causative mutations responsible for the phenotype, however, lagged far behind, limited by lack of molecular markers and high-throughput genotyping platforms. Next-generation sequencing technologies have revolutionized genomics, facilitating the process of identifying mutations underlying a phenotype of interest. Multiple mapping-by-sequencing or cloning-by-sequencing strategies were established towards fast gene discovery. In this study, we used mapping-by-sequencing to identify candidate genes within coarsely delimited genetic intervals, for two variegation mutants in barley – luteostrians and albostrians. After testing the approach using the example of the previously cloned albostrians gene HvAST, the gene HvClpC1 could be delimited as candidate gene for luteostrians. The mapping-by-sequencing strategy implemented here is generally suited for surveying barley mutant collections for phenotypes affecting fundamental processes of plant morphology, physiology and development.


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