Identifying trait clusters by linkage profiles: application in genetical genomics

نویسندگان

  • Joshua N. Sampson
  • Steven G. Self
چکیده

MOTIVATION Genes often regulate multiple traits. Identifying clusters of traits influenced by a common group of genes helps elucidate regulatory networks and can improve linkage mapping. METHODS We show that the Pearson correlation coefficient, rho L, between two LOD score profiles can, with high specificity and sensitivity, identify pairs of genes that have their transcription regulated by shared quantitative trait loci (QTL). Furthermore, using theoretical and/or empirical methods, we can approximate the distribution of rho L under the null hypothesis of no common QTL. Therefore, it is possible to calculate P-values and false discovery rates for testing whether two traits share common QTL. We then examine the properties of rho L through simulation and use rho L to cluster genes in a genetical genomics experiment examining Saccharomyces cerevisiae. RESULTS Simulations show that rho L can have more power than the clustering methods currently used in genetical genomics. Combining experimental results with Gene Ontology (GO) annotations show that genes within a purported cluster often share similar function. SOFTWARE R-code included in online Supplementary Material.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Functional genomics and genetical genomics approaches towards elucidating networks of genes affecting meat performance in pigs.

The benefit of functional genomics is to identify key pathways and functional networks of genes and candidate genes underlying the genetic control of phenotypes. Genetical genomics, i.e. the integration of genetic analysis and expression phenotypes, has the potential to uncover regulatory networks controlling the coordinated expression of genes and to map variation on the level of DNA affecting...

متن کامل

Regulatory network identification by genetical genomics: signaling downstream of the Arabidopsis receptor-like kinase ERECTA.

Gene expression differences between individuals within a species can be largely explained by differences in genetic background. The effect of genetic variants (alleles) of genes on expression can be studied in a multifactorial way by the application of genetical genomics or expression quantitative trait locus mapping. In this paper, we present a strategy to construct regulatory networks by the ...

متن کامل

Learning Gene Networks under SNP Perturbations Using eQTL Datasets

The standard approach for identifying gene networks is based on experimental perturbations of gene regulatory systems such as gene knock-out experiments, followed by a genome-wide profiling of differential gene expressions. However, this approach is significantly limited in that it is not possible to perturb more than one or two genes simultaneously to discover complex gene interactions or to d...

متن کامل

Quantile-based permutation thresholds for QTL hotspot analysis: a tutorial

QTL hotspots, groups of traits co-mapping to the same genomic location, are a common feature of genetical genomics studies. Genomic locations associated with many traits are biologically interesting since they may harbor influential regulators. Nonetheless, non-genetic mechanisms, uncontrolled environmental factors and unmeasured variables are capable of inducing a strong correlation structure ...

متن کامل

Methodological Advancement in Molecular Markers to Delimit the Gene(s) for Crop Improvement

Molecular markers, in recent years, have accelerated plant breeding methods significantly with an objective of crop improvement. At present a variety of molecular markers are available and the choice of using a particular type of marker depends on the user. With the advances in the area of genomics, new type and gene-derived markers as well as novel approaches such as genetical genomics, linkag...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Bioinformatics

دوره 24 7  شماره 

صفحات  -

تاریخ انتشار 2008