scholarly journals Genome-wide association study identifies SNPs in the MHC class II loci that are associated with self-reported history of whooping cough

2015 ◽  
Vol 24 (20) ◽  
pp. 5930-5939 ◽  
Author(s):  
George McMahon ◽  
Susan M. Ring ◽  
George Davey-Smith ◽  
Nicholas J. Timpson
2016 ◽  
Vol 83 (3) ◽  
pp. 265-268 ◽  
Author(s):  
Adrianna Mostowska ◽  
Kamil K. Hozyasz ◽  
Piotr Wójcicki ◽  
Barbara Biedziak ◽  
Joanna Wesoły ◽  
...  

The project “Searching for new genes and loci involved in cleft lip and palate in the Polish population – genome-wide association study” is a case-control study in a group of unrelated subjects with non-syndromic cleft lip with or without cleft palate (NSCL/P) and healthy individuals with no family history of clefting or other congenital disorders. The overall goal of this grant proposal is to identify novel genetic factors, which can play a significant role in the pathogenesis of orofacial clefts in the Polish population. To accomplish the proposed aim, a two stage genome-wide association study will be performed. In the first stage, Illumina's HumanOmni Express BeadChips arrays will be used to genotype over 700,000 polymorphisms in NSCL/P patients and controls. In the second stage, SNPs showing the most compelling association with the risk of orofacial clefts will be tested in an independent sample set using standard genotyping methods. This research project is expected to be completed in July 2015.


2011 ◽  
Vol 43 (4) ◽  
pp. 388-388
Author(s):  
Hyun Hor ◽  
Zoltán Kutalik ◽  
Yves Dauvilliers ◽  
Armand Valsesia ◽  
Gert J Lammers ◽  
...  

PLoS ONE ◽  
2010 ◽  
Vol 5 (3) ◽  
pp. e9723 ◽  
Author(s):  
Masahiro Nakajima ◽  
Atsushi Takahashi ◽  
Ikuyo Kou ◽  
Cristina Rodriguez-Fontenla ◽  
Juan J. Gomez-Reino ◽  
...  

2017 ◽  
Vol 7 (1) ◽  
Author(s):  
Raquel López-Mejías ◽  
F. David Carmona ◽  
Santos Castañeda ◽  
Fernanda Genre ◽  
Sara Remuzgo-Martínez ◽  
...  

2010 ◽  
Vol 42 (9) ◽  
pp. 786-789 ◽  
Author(s):  
Hyun Hor ◽  
Zoltán Kutalik ◽  
Yves Dauvilliers ◽  
Armand Valsesia ◽  
Gert J Lammers ◽  
...  

2021 ◽  
Vol 8 (1) ◽  
Author(s):  
Mai F. Minamikawa ◽  
Miyuki Kunihisa ◽  
Koji Noshita ◽  
Shigeki Moriya ◽  
Kazuyuki Abe ◽  
...  

AbstractHaplotypes provide useful information for genomics-based approaches, genomic prediction, and genome-wide association study. As a small number of superior founders have contributed largely to the breeding history of fruit trees, the information of founder haplotypes may be relevant for performing the genomics-based approaches in these plants. In this study, we proposed a method to estimate 14 haplotypes from 7 founders and automatically trace the haplotypes forward to apple parental (185 varieties) and breeding (659 F1 individuals from 16 full-sib families) populations based on 11,786 single-nucleotide polymorphisms, by combining multiple algorithms. Overall, 92% of the single-nucleotide polymorphisms information in the parental and breeding populations was characterized by the 14 founder haplotypes. The use of founder haplotype information improved the accuracy of genomic prediction in 7 traits and the resolution of genome-wide association study in 13 out of 27 fruit quality traits analyzed in this study. We also visualized the significant propagation of the founder haplotype with the largest genetic effect in genome-wide association study over the pedigree tree of the parental population. These results suggest that the information of founder haplotypes can be useful for not only genetic improvement of fruit quality traits in apples but also for understanding the selection history of founder haplotypes in the breeding program of Japanese apple varieties.


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