scholarly journals A genome-wide scan for a simulated data set using two newly developed methods

1999 ◽  
Vol 17 (S1) ◽  
pp. S621-S626
Author(s):  
Li Hsu ◽  
Corinne Aragaki ◽  
Filemon Quiaoit ◽  
Xiangjing Wang ◽  
Xiubin Xu ◽  
...  
Entropy ◽  
2019 ◽  
Vol 21 (8) ◽  
pp. 802
Author(s):  
Chun-xiao Sun ◽  
Yu Yang ◽  
Hua Wang ◽  
Wen-hu Wang

Chromatin immunoprecipitation combined with next-generation sequencing (ChIP-Seq) technology has enabled the identification of transcription factor binding sites (TFBSs) on a genome-wide scale. To effectively and efficiently discover TFBSs in the thousand or more DNA sequences generated by a ChIP-Seq data set, we propose a new algorithm named AP-ChIP. First, we set two thresholds based on probabilistic analysis to construct and further filter the cluster subsets. Then, we use Affinity Propagation (AP) clustering on the candidate cluster subsets to find the potential motifs. Experimental results on simulated data show that the AP-ChIP algorithm is able to make an almost accurate prediction of TFBSs in a reasonable time. Also, the validity of the AP-ChIP algorithm is tested on a real ChIP-Seq data set.


2011 ◽  
Vol 2 (1) ◽  
Author(s):  
Anna-Sapfo Malaspinas ◽  
Caroline Uhler

Rapid research progress in genotyping techniques have allowed large genome-wide associationstudies. Existing methods often focus on determining associations between single loci anda specic phenotype. However, a particular phenotype is usually the result of complex relationshipsbetween multiple loci and the environment. In this paper, we describe a two-stage methodfor detecting epistasis by combining the traditionally used single-locus search with a search formultiway interactions. Our method is based on an extended version of Fisher's exact test. Toperform this test, a Markov chain is constructed on the space of multidimensional contingencytables using the elements of a Markov basis as moves. We test our method on simulated data andcompare it to a two-stage logistic regression method and to a fully Bayesian method, showing thatwe are able to detect the interacting loci when other methods fail to do so. Finally, we apply ourmethod to a genome-wide data set consisting of 685 dogs and identify epistasis associated withcanine hair length for four pairs of single nucleotide polymorphisms (SNPs).


2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Olusola Olawoye ◽  
Chimdi Chuka-Okosa ◽  
Onoja Akpa ◽  
Tony Realini ◽  
Michael Hauser ◽  
...  

Abstract Background This report describes the design and methodology of the “Eyes of Africa: The Genetics of Blindness,” a collaborative study funded through the Human Heredity and Health in Africa (H3Africa) program of the National Institute of Health. Methods This is a case control study that is collecting a large well phenotyped data set among glaucoma patients and controls for a genome wide association study. (GWAS). Multiplex families segregating Mendelian forms of early-onset glaucoma will also be collected for exome sequencing. Discussion A total of 4500 cases/controls have been recruited into the study at the end of the 3rd funded year of the study. All these participants have been appropriately phenotyped and blood samples have been received from these participants. Recent GWAS of POAG in African individuals demonstrated genome-wide significant association with the APBB2 locus which is an association that is unique to individuals of African ancestry. This study will add to the existing knowledge and understanding of POAG in the African population.


2006 ◽  
Vol 38 (7) ◽  
pp. 794-800 ◽  
Author(s):  
Anelia Horvath ◽  
Sosipatros Boikos ◽  
Christoforos Giatzakis ◽  
Audrey Robinson-White ◽  
Lionel Groussin ◽  
...  

Genetics ◽  
2013 ◽  
Vol 196 (3) ◽  
pp. 829-840 ◽  
Author(s):  
Timothy M. Beissinger ◽  
Candice N. Hirsch ◽  
Brieanne Vaillancourt ◽  
Shweta Deshpande ◽  
Kerrie Barry ◽  
...  

1999 ◽  
Vol 17 (S1) ◽  
pp. S49-S54 ◽  
Author(s):  
J.S. Barnholtz ◽  
M. de Andrade ◽  
G.P. Page ◽  
T.M. King ◽  
L.E. Peterson ◽  
...  

2007 ◽  
Vol 144B (2) ◽  
pp. 193-199 ◽  
Author(s):  
M.A. Escamilla ◽  
A. Ontiveros ◽  
H. Nicolini ◽  
H. Raventos ◽  
R. Mendoza ◽  
...  

2021 ◽  
Vol 7 (29) ◽  
pp. eabc0776
Author(s):  
Nathan K. Schaefer ◽  
Beth Shapiro ◽  
Richard E. Green

Many humans carry genes from Neanderthals, a legacy of past admixture. Existing methods detect this archaic hominin ancestry within human genomes using patterns of linkage disequilibrium or direct comparison to Neanderthal genomes. Each of these methods is limited in sensitivity and scalability. We describe a new ancestral recombination graph inference algorithm that scales to large genome-wide datasets and demonstrate its accuracy on real and simulated data. We then generate a genome-wide ancestral recombination graph including human and archaic hominin genomes. From this, we generate a map within human genomes of archaic ancestry and of genomic regions not shared with archaic hominins either by admixture or incomplete lineage sorting. We find that only 1.5 to 7% of the modern human genome is uniquely human. We also find evidence of multiple bursts of adaptive changes specific to modern humans within the past 600,000 years involving genes related to brain development and function.


2003 ◽  
Vol 123A (2) ◽  
pp. 140-147 ◽  
Author(s):  
Diego F. Wyszynski ◽  
Hasan Albacha-Hejazi ◽  
Mohammed Aldirani ◽  
Moustafa Hammod ◽  
Hikmat Shkair ◽  
...  

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