ArticleJournal of bioinformatics and computational biology2011
A compressed sensing based approach for subtyping of leukemia from gene expression data.
Article in Journal of bioinformatics and computational biology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
8 citing papers in PubMed.
- Linear programming based computational technique for leukemia classification using gene expression profile.PloS one · 2023Article
- Collaborative representation-based classification of microarray gene expression data.PloS one · 2017Article
- Sparse models for correlative and integrative analysis of imaging and genetic data.Journal of neuroscience methods · 2014Review
- Sparse representation based biomarker selection for schizophrenia with integrated analysis of fMRI and SNPs.NeuroImage · 2014Review
- Highly accurate recognition of human postures and activities through classification with rejection.IEEE journal of biomedical and health informatics · 2014Article
- Subtyping glioblastoma by combining miRNA and mRNA expression data using compressed sensing-based approach.EURASIP journal on bioinformatics & systems biology · 2013Article
- Integrating fMRI and SNP data for biomarker identification for schizophrenia with a sparse representation based variable selection method.BMC medical genomics · 2013Article
- Subtyping of Gliomaby Combining Gene Expression and CNVs Data Based on a Compressive Sensing Approach.Advancements in genetic engineering · 2012Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
Abstract
With the development of genomic techniques, the demand for new methods that can handle high-throughput genome-wide data effectively is becoming stronger than ever before. Compressed sensing (CS) is an emerging approach in statistics and signal processing. With the CS theory, a signal can be uniquely reconstructed or approximated from its sparse representations, which can therefore better distinguish different types of signals. However, the application of CS approach to genome-wide data analysis has been rarely investigated. We propose a novel CS-based approach for genomic data classification and test its performance in the subtyping of leukemia through gene expression analysis. The detection of subtypes of cancers such as leukemia according to different genetic markups is significant, which holds promise for the individualization of therapies and improvement of treatments. In our work, four statistical features were employed to select significant genes for the classification. With our selected genes out of 7,129 ones, the proposed CS method achieved a classification accuracy of 97.4% when evaluated with the cross validation and 94.3% when evaluated with another independent data set. The robustness of the method to noise was also tested, giving good performance. Therefore, this work demonstrates that the CS method can effectively detect subtypes of leukemia, implying improved accuracy of diagnosis of leukemia.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.