Search PubMed⌕ Search

PubMed · 16180916

Diagnostic pattern recognition on gene-expression profile data by using one-class classification.

Abstract

In this paper, we perform diagnostic pattern recognition on a gene-expression profile data set by using one-class classification. Unlike conventional multiclass classifiers, the one-class (OC) classifier is built on one class only. For optimal performance, it accepts samples coming from the class used for training and rejects all samples from other classes. We evaluate six OC classifiers: the Gaussian model, Parzen windows, support vector data description (with two types of kernels: inner product and Gaussian), nearest neighbor data description, K-means, and PCA on three gene-expression profile data sets, those being an SRBCT data set, a Colon data set, and a Leukemia data set. Providing there is a good splitting of training and test samples and feature selection, most OC classifiers can produce high quality results. Parzen windows and support vector data description are "over-strict" in most cases, while nearest neighbor data description is "over-loose". Other classifiers are intermediate between these two extremes. The main difficulty for the OC classifier is it is difficult to obtain an optimum decision threshold if there are a limited number of training samples.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Yun Xu, Richard G Brereton. Diagnostic pattern recognition on gene-expression profile data by using one-class classification.. https://doi.org/10.1021/ci049726v

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

KEEP EXPLORING

Related citations

Neuromedin U stimulates contraction of human long saphenous vein and gastrointestinal smooth muscle in vitro.

The neuropeptide Neuromedin U (NMU) stimulates smooth muscle contraction, and modulates local blood flow and adrenocortical function via two endogenous receptors, NMU1 and NMU2. Although its amino-acid sequence is highly conserved across species, the physiological effects of NMU are variable between species and little is known of its effects on human tissues. We have examined the contractile effects of NMU-25 on human smooth muscles of the gastrointestinal (GI) tract (ascending colon, gallbladder) and long saphenous vein (LSV) using in vitro organ bath bioassays. From LSV, ileum, gallbladder, caecum and colon, NMU receptor transcripts were amplified by RT-PCR and expression levels were determined by semi-quantitative scanning densitometry. NMU-25 produced a concentration-dependent, sustained contraction of isolated smooth muscle (p[A](50)+/-s.e.m., ascending colon, 8.93+/-0.18; gallbladder, 7.01+/-0.15; LSV, 8.67+/-0.09). NMU1 and NMU2 receptor transcription was detected in all tissues; transcription of both receptors was similar in gallbladder, but NMU1 receptor transcription was predominant in the sigmoid colon and LSV. In summary, these studies indicate that NMU may control tone in the human GI tract and LSV through an action on smooth muscle. Development of NMU receptor subtype-selective ligands will aid the further elucidation of the physiological roles of NMU and its two receptors.

Colon↗

Colon-specific drug delivery: Influence of solution reticulation properties upon pectin beads performance.

In this study, pectinate gel beads were produced by ionotropic gelation method with different solutions of cross-linking agents and ketoprofen was entrapped as model drug. The influence of these formulation parameters was investigated upon bead properties and upon their performance to target the colon. Zinc pectinate beads obtained with 10% of counter-ions solution at pH 1.6 exhibited the strongest gel network due to "egg-box" dimmer formation helped by hydrogen bonding. Furthermore the gel network formed at low pH was arranged in a compact three-fold conformation. Thus, this matrix structure in enteric capsules induced the lowest drug release in the upper gastro-intestinal tract (pH 1.2 following by pH 7.4). However ketoprofen release occurred specifically in the colon thanks to the presence of pectinolytic enzymes and the release rate can be modulated by the counter-ion concentration during the reticulation process. Therefore this approach using pectinate beads is very promising as efficient carrier for specific delivery of drug into the colon, after oral administration.

Colon↗