Results 41 to 50 of about 159,661 (256)

A flexible network-based imputing-and-fusing approach towards the identification of cell types from single-cell RNA-seq data

open access: yesBMC Bioinformatics, 2020
Background Single-cell RNA sequencing (scRNA-seq) provides an effective tool to investigate the transcriptomic characteristics at the single-cell resolution.
Yang Qi   +3 more
doaj   +1 more source

Impact of Asymptomatic Intracranial Hemorrhage on Outcome After Endovascular Stroke Treatment

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background Endovascular treatment (EVT) achieves high rates of recanalization in acute large‐vessel occlusion (LVO) stroke, but functional recovery remains heterogeneous. While symptomatic intracranial hemorrhage (sICH) has been well studied, the prognostic impact of asymptomatic intracranial hemorrhage (aICH) after EVT is less certain ...
Shihai Yang   +22 more
wiley   +1 more source

Multiple imputation for estimation of an occurrence rate in cohorts with attrition and discrete follow-up time points: a simulation study

open access: yesBMC Medical Research Methodology, 2010
Background In longitudinal cohort studies, subjects may be lost to follow-up at any time during the study. This leads to attrition and thus to a risk of inaccurate and biased estimations.
Soullier Noémie   +2 more
doaj   +1 more source

SICE: an improved missing data imputation technique

open access: yesJournal of Big Data, 2020
In data analytics, missing data is a factor that degrades performance. Incorrect imputation of missing values could lead to a wrong prediction. In this era of big data, when a massive volume of data is generated in every second, and utilization of these ...
Shahidul Islam Khan   +1 more
doaj   +1 more source

Missing Value Imputation for RNA-Sequencing Data Using Statistical Models: A Comparative Study [PDF]

open access: yesJournal of Statistical Theory and Applications (JSTA), 2016
RNA-seq technology has been widely used as an alternative approach to traditional microarrays in transcript analysis. Sometimes gene expression by sequencing, which generates RNA-seq data set, may have missing read counts.
Taban Baghfalaki   +2 more
doaj   +1 more source

Five‐Year Disease Progression in Synuclein Seeding Positive Sporadic Parkinson's Disease

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To provide a comprehensive description of disease progression in synuclein seeding assay (SAA) positive sporadic Parkinson Disease participants, using Neuronal Synuclein Disease integrated biological and functional impairment staging framework.
Paulina Gonzalez‐Latapi   +19 more
wiley   +1 more source

The ability of different imputation methods for missing values in mental measurement questionnaires

open access: yesBMC Medical Research Methodology, 2020
Background Incomplete data are of particular important influence in mental measurement questionnaires. Most experts, however, mostly focus on clinical trials and cohort studies and generally pay less attention to this deficiency. We aim is to compare the
Xueying Xu   +5 more
doaj   +1 more source

Evaluation of Odor Prediction Model Performance and Variable Importance according to Various Missing Imputation Methods

open access: yesApplied Sciences, 2022
The aim of this study is to ascertain the most suitable model for predicting complex odors using odor substance data that has a small number of data and a large number of missing data.
Do-Hyun Lee   +3 more
doaj   +1 more source

A Prospective Study of Individuals at Risk of Multiple Sclerosis Informs the Design of Primary Prevention Studies

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective In multiple sclerosis, the optimal time for deploying a therapeutic intervention is before the central nervous system is damaged; given the success of trials treating the earliest stage of MS, the radiologically isolated syndrome, developing primary prevention strategies is an important next challenge.
Amy W. Laitinen   +7 more
wiley   +1 more source

Onasemnogene Abeparvovec in Type I Spinal Muscular Atrophy: 24‐Month Follow‐Up From the Italian Registry

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Onasemnogene abeparvovec (OA) is an AAV9‐based gene therapy for spinal muscular atrophy type I (SMA I). Real‐world outcomes show increased response variability compared to clinical trials, and follow‐up data beyond 12–18 months are limited.
Marika Pane   +43 more
wiley   +1 more source

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