Cargando…

The INTERPRET Decision-Support System version 3.0 for evaluation of Magnetic Resonance Spectroscopy data from human brain tumours and other abnormal brain masses

BACKGROUND: Proton Magnetic Resonance (MR) Spectroscopy (MRS) is a widely available technique for those clinical centres equipped with MR scanners. Unlike the rest of MR-based techniques, MRS yields not images but spectra of metabolites in the tissues. In pathological situations, the MRS profile cha...

Descripción completa

Detalles Bibliográficos
Autores principales:	Pérez-Ruiz, Alexander, Julià-Sapé, Margarida, Mercadal, Guillem, Olier, Iván, Majós, Carles, Arús, Carles
Formato:	Texto
Lenguaje:	English
Publicado:	BioMed Central 2010
Materias:	Software
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3004884/ https://www.ncbi.nlm.nih.gov/pubmed/21114820 http://dx.doi.org/10.1186/1471-2105-11-581

Ejemplares similares

SpectraClassifier 1.0: a user friendly, automated MRS-based classifier-development system
por: Ortega-Martorell, Sandra, et al.
Publicado: (2010)

From raw data to data-analysis for magnetic resonance spectroscopy – the missing link: jMRUI2XML
por: Mocioiu, Victor, et al.
Publicado: (2015)

Non-negative matrix factorisation methods for the spectral decomposition of MRS data from human brain tumours
por: Ortega-Martorell, Sandra, et al.
Publicado: (2012)

A Novel Semi-Supervised Methodology for Extracting Tumor Type-Specific MRS Sources in Human Brain Data
por: Ortega-Martorell, Sandra, et al.
Publicado: (2013)

Using Single-Voxel Magnetic Resonance Spectroscopy Data Acquired at 1.5T to Classify Multivoxel Data at 3T: A Proof-of-Concept Study
por: Ungan, Gülnur, et al.
Publicado: (2023)

Convex Non-Negative Matrix Factorization for Brain Tumor Delimitation from MRSI Data
por: Ortega-Martorell, Sandra, et al.
Publicado: (2012)

Embedding MRI information into MRSI data source extraction improves brain tumour delineation in animal models
por: Ortega-Martorell, Sandra, et al.
Publicado: (2019)

Multiproject–multicenter evaluation of automatic brain tumor classification by magnetic resonance spectroscopy
por: García-Gómez, Juan M., et al.
Publicado: (2008)

Brain metabolic pattern analysis using a magnetic resonance spectra classification software in experimental stroke
por: Jiménez-Xarrié, Elena, et al.
Publicado: (2017)

Improving the classification of brain tumors in mice with perturbation enhanced (PE)-MRSI
por: Simões, Rui V, et al.
Publicado: (2010)

DCE@urLAB: a dynamic contrast-enhanced MRI pharmacokinetic analysis tool for preclinical data
por: Ortuño, Juan E, et al.
Publicado: (2013)

Adobe Acrobat versión 3.0
Publicado: (1997)

Prototyping a precision oncology 3.0 rapid learning platform
por: Sweetnam, Connor, et al.
Publicado: (2018)

Strategies for annotation and curation of translational databases: the eTUMOUR project
por: Julià-Sapé, Margarida, et al.
Publicado: (2012)

Module-A. Version 1.0
por: Jekel, James F.
Publicado: (1988)

puma 3.0: improved uncertainty propagation methods for gene and transcript expression analysis
por: Liu, Xuejun, et al.
Publicado: (2013)

PFAAT version 2.0: A tool for editing, annotating, and analyzing multiple sequence alignments
por: Caffrey, Daniel R, et al.
Publicado: (2007)

Metabolomics of Therapy Response in Preclinical Glioblastoma: A Multi-Slice MRSI-Based Volumetric Analysis for Noninvasive Assessment of Temozolomide Treatment
por: Arias-Ramos, Nuria, et al.
Publicado: (2017)

Unraveling response to temozolomide in preclinical GL261 glioblastoma with MRI/MRSI using radiomics and signal source extraction
por: Núñez, Luis Miguel, et al.
Publicado: (2020)

GeneOrder3.0: Software for comparing the order of genes in pairs of small bacterial genomes
por: Celamkoti, Srikanth, et al.
Publicado: (2004)

Encompassing new use cases - level 3.0 of the HUPO-PSI format for molecular interactions
por: Sivade (Dumousseau), M., et al.
Publicado: (2018)

ECL 3.0: a sensitive peptide identification tool for cross-linking mass spectrometry data analysis
por: Zhou, Chen, et al.
Publicado: (2023)

shRNAPred (version 1.0): An open source and standalone software for short hairpin RNA (shRNA) prediction
por: Singh, Nishtha, et al.
Publicado: (2012)

The Virtual Electrode Recording Tool for EXtracellular Potentials (VERTEX) Version 2.0: Modelling in vitro electrical stimulation of brain tissue
por: Thornton, Christopher, et al.
Publicado: (2019)

MultiDataSet: an R package for encapsulating multiple data sets with application to omic data integration
por: Hernandez-Ferrer, Carles, et al.
Publicado: (2017)

TranscriptomeBrowser 3.0: introducing a new compendium of molecular interactions and a new visualization tool for the study of gene regulatory networks
por: Lepoivre, Cyrille, et al.
Publicado: (2012)

Pash 3.0: A versatile software package for read mapping and integrative analysis of genomic and epigenomic variation using massively parallel DNA sequencing
por: Coarfa, Cristian, et al.
Publicado: (2010)

NetMHCpan-3.0; improved prediction of binding to MHC class I molecules integrating information from multiple receptor and peptide length datasets
por: Nielsen, Morten, et al.
Publicado: (2016)

MeShClust v3.0: high-quality clustering of DNA sequences using the mean shift algorithm and alignment-free identity scores
por: Girgis, Hani Z.
Publicado: (2022)

QS version 3.0
por: Chang, Yih-Long
Publicado: (1995)

Software for interpreting cardiopulmonary exercise tests
por: Ross, Robert M, et al.
Publicado: (2007)

brain-coX: investigating and visualising gene co-expression in seven human brain transcriptomic datasets
por: Freytag, Saskia, et al.
Publicado: (2017)

R.ROSETTA: an interpretable machine learning framework
por: Garbulowski, Mateusz, et al.
Publicado: (2021)

WEScover: selection between clinical whole exome sequencing and gene panel testing
por: Lee, In-Hee, et al.
Publicado: (2021)

JCGA: the Japanese version of the Cancer Genome Atlas and its contribution to the interpretation of gene alterations detected in clinical cancer genome sequencing
por: Serizawa, Masakuni, et al.
Publicado: (2021)

affy2sv: an R package to pre-process Affymetrix CytoScan HD and 750K arrays for SNP, CNV, inversion and mosaicism calling
por: Hernandez-Ferrer, Carles, et al.
Publicado: (2015)

Development of robust discriminant equations for assessing subtypes of glioblastoma biopsies
por: Castells, X, et al.
Publicado: (2012)

Mining gene expression data by interpreting principal components
por: Roden, Joseph C, et al.
Publicado: (2006)

Genome analysis and knowledge-driven variant interpretation with TGex
por: Dahary, Dvir, et al.
Publicado: (2019)

ABrainVis: an android brain image visualization tool
por: Osorio, Ignacio, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_8u03asemk8g6ihqhb1jcvqbq85