Literature DB >> 24458951

The most informative spacing test effectively discovers biologically relevant outliers or multiple modes in expression.

Iwona Pawlikowska1, Gang Wu, Michael Edmonson, Zhifa Liu, Tanja Gruber, Jinghui Zhang, Stan Pounds.   

Abstract

SUMMARY: Several outlier and subgroup identification statistics (OASIS) have been proposed to discover transcriptomic features with outliers or multiple modes in expression that are indicative of distinct biological processes or subgroups. Here, we borrow ideas from the OASIS methods in the bioinformatics and statistics literature to develop the 'most informative spacing test' (MIST) for unsupervised detection of such transcriptomic features. In an example application involving 14 cases of pediatric acute megakaryoblastic leukemia, MIST more robustly identified features that perfectly discriminate subjects according to gender or the presence of a prognostically relevant fusion-gene than did seven other OASIS methods in the analysis of RNA-seq exon expression, RNA-seq exon junction expression and micorarray exon expression data. MIST was also effective at identifying features related to gender or molecular subtype in an example application involving 157 adult cases of acute myeloid leukemia. AVAILABILITY: MIST will be freely available in the OASIS R package at http://www.stjuderesearch.org/site/depts/biostats CONTACT: stanley.pounds@stjude.org SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

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Year:  2014        PMID: 24458951      PMCID: PMC4068004          DOI: 10.1093/bioinformatics/btu039

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  15 in total

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  7 in total

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2.  Prognostic Significance of Major Histocompatibility Complex Class II Expression in Pediatric Adrenocortical Tumors: A St. Jude and Children's Oncology Group Study.

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4.  Pan-cancer transcriptome analysis reveals long noncoding RNAs with conserved function.

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5.  Discovery of regulatory noncoding variants in individual cancer genomes by using cis-X.

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Review 7.  How Machine Learning and Statistical Models Advance Molecular Diagnostics of Rare Disorders Via Analysis of RNA Sequencing Data.

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  7 in total

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