Cargando…

Structure-revealing data fusion

BACKGROUND: Analysis of data from multiple sources has the potential to enhance knowledge discovery by capturing underlying structures, which are, otherwise, difficult to extract. Fusing data from multiple sources has already proved useful in many applications in social network analysis, signal proc...

Descripción completa

Detalles Bibliográficos
Autores principales:	Acar, Evrim, Papalexakis, Evangelos E, Gürdeniz, Gözde, Rasmussen, Morten A, Lawaetz, Anders J, Nilsson, Mathias, Bro, Rasmus
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2014
Materias:	Methodology Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4117975/ https://www.ncbi.nlm.nih.gov/pubmed/25015427 http://dx.doi.org/10.1186/1471-2105-15-239

Ejemplares similares

Data fusion in metabolomic cancer diagnostics
por: Bro, Rasmus, et al.
Publicado: (2012)

Unraveling Diagnostic Biomarkers of Schizophrenia Through Structure-Revealing Fusion of Multi-Modal Neuroimaging Data
por: Acar, Evrim, et al.
Publicado: (2019)

The Anatomy of American Football: Evidence from 7 Years of NFL Game Data
por: Pelechrinis, Konstantinos, et al.
Publicado: (2016)

Large-scale benchmarking reveals false discoveries and count transformation sensitivity in 16S rRNA gene amplicon data analysis methods used in microbiome studies
por: Thorsen, Jonathan, et al.
Publicado: (2016)

Adaptive granularity in tensors: A quest for interpretable structure
por: Pasricha, Ravdeep S., et al.
Publicado: (2022)

The Effect of LC-MS Data Preprocessing Methods on the Selection of Plasma Biomarkers in Fed vs. Fasted Rats
por: Gürdeniz, Gözde, et al.
Publicado: (2012)

Enhanced ranking of PknB Inhibitors using data fusion methods
por: Seal, Abhik, et al.
Publicado: (2013)

Assembly of a gene sequence tag microarray by reversible biotin-streptavidin capture for transcript analysis of Arabidopsis thaliana
por: Wirta, Valtteri, et al.
Publicado: (2005)

The Metabolomics of Childhood Atopic Diseases: A Comprehensive Pathway-Specific Review
por: Schjødt, Mette S., et al.
Publicado: (2020)

Gene Fusion Markup Language: a prototype for exchanging gene fusion data
por: Kalyana-Sundaram, Shanker, et al.
Publicado: (2012)

Multiway modeling and analysis in stem cell systems biology
por: Yener, Bülent, et al.
Publicado: (2008)

Development of an algorithm to identify urgent referrals for suspected cancer from the Danish Primary Care Referral Database
por: Toftegaard, Berit Skjødeberg, et al.
Publicado: (2016)

An exploratory data analysis method to reveal modular latent structures in high-throughput data
por: Yu, Tianwei
Publicado: (2010)

Life history data from the gateway to global ageing data platform: resources for studying life courses across Europe
por: Wahrendorf, Morten, et al.
Publicado: (2023)

Calculation of Tajima’s D and other neutrality test statistics from low depth next-generation sequencing data
por: Korneliussen, Thorfinn Sand, et al.
Publicado: (2013)

CLOVE: classification of genomic fusions into structural variation events
por: Schröder, Jan, et al.
Publicado: (2017)

SENSory re-learning of the UPPer limb (SENSUPP) after stroke: development and description of a novel intervention using the TIDieR checklist
por: Carlsson, Håkan, et al.
Publicado: (2021)

Using multiple imputation to deal with missing data and attrition in longitudinal studies with repeated measures of patient-reported outcomes
por: Biering, Karin, et al.
Publicado: (2015)

Network construction and structure detection with metagenomic count data
por: Liu, Zhenqiu, et al.
Publicado: (2015)

Independent component analysis reveals new and biologically significant structures in micro array data
por: Frigyesi, Attila, et al.
Publicado: (2006)

Fusion of wildlife tracking and satellite geomagnetic data for the study of animal migration
por: Benitez-Paez, Fernando, et al.
Publicado: (2021)

Structural Zero Data of COVID-19 Discovers Exodus Probabilities
por: Shanmugam, Ramalingam, et al.
Publicado: (2021)

Existing data sources for clinical epidemiology: The Danish National Database of Reimbursed Prescriptions
por: Johannesdottir, Sigrun Alba, et al.
Publicado: (2012)

Open-access synthetic spike-in mRNA-seq data for cancer gene fusions
por: Tembe, Waibhav D, et al.
Publicado: (2014)

Saliva as a sampling source for the detection of leukemic fusion transcripts
por: Chen, Dongmei, et al.
Publicado: (2014)

A simple, flexible and efficient PCR-fusion/Gateway cloning procedure for gene fusion, site-directed mutagenesis, short sequence insertion and domain deletions and swaps
por: Atanassov, Ivan I, et al.
Publicado: (2009)

Existing data sources for clinical epidemiology: Scandinavian Cohort for osteonecrosis of the jaw – work in progress and challenges
por: Schiodt, Morten, et al.
Publicado: (2015)

Power-Hop: A Pervasive Observation for Real Complex Networks
por: Papalexakis, Evangelos, et al.
Publicado: (2016)

Zero problems with compositional data of physical behaviors: a comparison of three zero replacement methods
por: Rasmussen, Charlotte Lund, et al.
Publicado: (2020)

Simulation of normal and pathological gaits using a fusion knowledge strategy
por: Martínez, Fabio, et al.
Publicado: (2013)

Subtracting the sequence bias from partially digested MNase-seq data reveals a general contribution of TFIIS to nucleosome positioning
por: Gutiérrez, Gabriel, et al.
Publicado: (2017)

Effective visualization of integrated knowledge and data to enable informed decisions in drug development and translational medicine
por: Brynne, Lena, et al.
Publicado: (2013)

A new pipeline for structural characterization and classification of RNA-Seq microbiome data
por: Racedo, Sebastian, et al.
Publicado: (2021)

Mining, analyzing, and integrating viral signals from metagenomic data
por: Zheng, Tingting, et al.
Publicado: (2019)

L(2)-norm multiple kernel learning and its application to biomedical data fusion
por: Yu, Shi, et al.
Publicado: (2010)

Fusion of metabolomics and proteomics data for biomarkers discovery: case study on the experimental autoimmune encephalomyelitis
por: Blanchet, Lionel, et al.
Publicado: (2011)

A fast detection of fusion genes from paired-end RNA-seq data
por: Vu, Trung Nghia, et al.
Publicado: (2018)

Transcriptomics Signature from Next-Generation Sequencing Data Reveals New Transcriptomic Biomarkers Related to Prostate Cancer
por: Alkhateeb, Abedalrhman, et al.
Publicado: (2019)

Bridging experiment and theory: a template for unifying NMR data and electronic structure calculations
por: Brown, David M. L., et al.
Publicado: (2016)

Vertical Transfer of Metabolites Detectable from Newborn’s Dried Blood Spot Samples Using UPLC-MS: A Chemometric Study
por: Olarini, Alessandra, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_04i77kkqvrcttamofp2ok15sur