The emerging era of genomic data integration for analyzing splice isoform function
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Genes Caught In Flagranti: Integrating Renal Transcriptional Profiles With Genotypes and PhenotypesTracks through the genome to physiological eventsTargeted capture and resequencing of 1040 genes reveal environmentally driven functional variation in grey wolvesIsoform-level brain expression profiling of the spermidine/spermine N1-Acetyltransferase1 (SAT1) gene in major depression and suicideMIsoMine: a genome-scale high-resolution data portal of expression, function and networks at the splice isoform level in the mouseRevisiting the identification of canonical splice isoforms through integration of functional genomics and proteomics evidence.GeneFriends: a human RNA-seq-based gene and transcript co-expression databaseAlternative applications for distinct RNA sequencing strategies.Do housekeeping genes exist?Union Exon Based Approach for RNA-Seq Gene Quantification: To Be or Not to Be?Actionable clinical decisions based on comprehensive genomic evaluation in asymptomatic adults.Functional divergence and convergence between the transcript network and gene network in lung adenocarcinoma.Computational Inferences of the Functions of Alternative/Noncanonical Splice Isoforms Specific to HER2+/ER-/PR- Breast Cancers, a Chromosome 17 C-HPP Study.MI-PVT: A Tool for Visualizing the Chromosome-Centric Human ProteomeFunctional Networks of Highest-Connected Splice Isoforms: From The Chromosome 17 Human Proteome Project.Identification of protein features encoded by alternative exons using Exon Ontology.Transcriptome profile of the human placenta.Whole-transcriptome brain expression and exon-usage profiling in major depression and suicide: evidence for altered glial, endothelial and ATPase activity.A proteogenomic approach to understand splice isoform functions through sequence and expression-based computational modeling.A Network of Splice Isoforms for the MouseVariance component testing for identifying differentially expressed genes in RNA-seq dataBRWLDA: bi-random walks for predicting lncRNA-disease associations.BreakSeek: a breakpoint-based algorithm for full spectral range INDEL detection.A Transcriptional Map of the Renal Tubule: Linking Structure to Function.Human genes with a greater number of transcript variants tend to show biological features of housekeeping and essential genes.Framework and resource for more than 11,000 gene-transcript-protein-reaction associations in human metabolism.Exploiting differential RNA splicing patterns: a potential new group of therapeutic targets in cancer.Bioinformatics challenges and perspectives when studying the effect of epigenetic modifications on alternative splicing.
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P2860
The emerging era of genomic data integration for analyzing splice isoform function
description
2014 nî lūn-bûn
@nan
2014 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2014年の論文
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2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
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name
The emerging era of genomic data integration for analyzing splice isoform function
@ast
The emerging era of genomic data integration for analyzing splice isoform function
@en
The emerging era of genomic data integration for analyzing splice isoform function
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The emerging era of genomic data integration for analyzing splice isoform function
@ast
The emerging era of genomic data integration for analyzing splice isoform function
@en
The emerging era of genomic data integration for analyzing splice isoform function
@nl
prefLabel
The emerging era of genomic data integration for analyzing splice isoform function
@ast
The emerging era of genomic data integration for analyzing splice isoform function
@en
The emerging era of genomic data integration for analyzing splice isoform function
@nl
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P3181
P1433
P1476
The emerging era of genomic data integration for analyzing splice isoform function
@en
P2093
Hong-Dong Li
Rajasree Menon
P2860
P304
P3181
P356
10.1016/J.TIG.2014.05.005
P407
P577
2014-06-17T00:00:00Z