PubMed Health⌕ Search

PubMed · 11802432

[Computational analysis of gene expression patterns].

Abstract

The source did not provide an abstract. Follow the original record for more information.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

S Morishita, J Sese. 2001. [Computational analysis of gene expression patterns].. https://pubmed.ncbi.nlm.nih.gov/11802432/

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

Clustering individuals using INMTD: a novel versatile multi-view embedding framework integrating omics and imaging data.

MOTIVATION: Combining omics and images can lead to a more comprehensive clustering of individuals than classic single-view approaches. Among the various approaches for multi-view clustering, nonnegative matrix tri-factorization (NMTF) and nonnegative Tucker decomposition (NTD) are advantageous in learning low-rank embeddings with promising interpretability. Besides, there is a need to handle unwanted drivers of clusterings (i.e. confounders). RESULTS: In this work, we introduce a novel multi-view clustering method based on NMTF and NTD, named INMTD, which integrates omics and 3D imaging data to derive unconfounded subgroups of individuals. According to the adjusted Rand index, INMTD outperformed other clustering methods on a synthetic dataset with known clusters. In the application to real-life facial-genomic data, INMTD generated biologically relevant embeddings for individuals, genetics, and facial morphology. By removing confounded embedding vectors, we derived an unconfounded clustering with better internal and external quality; the genetic and facial annotations of each derived subgroup highlighted distinctive characteristics. In conclusion, INMTD can effectively integrate omics data and 3D images for unconfounded clustering with biologically meaningful interpretation. AVAILABILITY AND IMPLEMENTATION: INMTD is freely available at https://github.com/ZuqiLi/INMTD.

Cluster Analysis↗

Fuzzy species among recombinogenic bacteria.

BACKGROUND: It is a matter of ongoing debate whether a universal species concept is possible for bacteria. Indeed, it is not clear whether closely related isolates of bacteria typically form discrete genotypic clusters that can be assigned as species. The most challenging test of whether species can be clearly delineated is provided by analysis of large populations of closely-related, highly recombinogenic, bacteria that colonise the same body site. We have used concatenated sequences of seven house-keeping loci from 770 strains of 11 named Neisseria species, and phylogenetic trees, to investigate whether genotypic clusters can be resolved among these recombinogenic bacteria and, if so, the extent to which they correspond to named species. RESULTS: Alleles at individual loci were widely distributed among the named species but this distorting effect of recombination was largely buffered by using concatenated sequences, which resolved clusters corresponding to the three species most numerous in the sample, N. meningitidis, N. lactamica and N. gonorrhoeae. A few isolates arose from the branch that separated N. meningitidis from N. lactamica leading us to describe these species as 'fuzzy'. CONCLUSION: A multilocus approach using large samples of closely related isolates delineates species even in the highly recombinogenic human Neisseria where individual loci are inadequate for the task. This approach should be applied by taxonomists to large samples of other groups of closely-related bacteria, and especially to those where species delineation has historically been difficult, to determine whether genotypic clusters can be delineated, and to guide the definition of species.

Cluster Analysis↗

REML and ML estimation for clustered grouped survival data.

Clustered grouped survival data arise naturally in clinical medicine and biological research. For example, in a randomized clinical trial, the variable of interest is the time to occurrence of a certain event with or without a new treatment and the data are collected from possibly correlated subjects from independent clusters. However it is sometimes impossible or too expensive to monitor the experimental subjects continuously. The subjects are examined regularly and the continuous survival data are thus grouped into a discrete time scale. With such a design, researchers are mainly interested in the effectiveness of the new treatment as well as the correlation among subjects from the same cluster, namely the intracluster correlation. This paper suggests a random effects approach to the estimation of the regression parameter with various choices of regression model and also the dependence parameter which characterizes the intracluster correlation. Time dependent covariates can be accommodated in the proposed model, and the estimation procedure will not be further complicated with large cluster sizes. The proposed method is applied to the data from the Diabetic Retinopathy Study, the objective of which is to evaluate the effectiveness of laser photocoagulation in delaying or preventing the onset of blindness in the left and right eyes of individuals with diabetes-associated retinopathy. The intracluster correlation using a grouped proportional hazards regression model can be estimated and the relationship between the regression parameter estimates based on the random effects approach and the marginal approach using a dynamic logistic regression model are discussed. Results from a simulation study of the proposed method are also presented.

Cluster Analysis↗