Biology subjects

Russell Poldrack

Publications and source records attributed to Russell Poldrack.

6 recordsLinked to original sources

bioRxiv2016

BIDS Apps: Improving ease of use, accessibility and reproducibility of neuroimaging data analysis methods

The rate of progress in human neurosciences is limited by the inability to easily apply a wide range of analysis methods to the plethora of different datasets acquired in labs around the world. In this work, we introduce a framework for creating, testing, versioning and archiving portable applications for analyzing neuroimaging data organized and described in compliance with the Brain Imaging Data Structure (BIDS). The portability of these applications (BIDS Apps) is achieved by using container technologies that encapsulate all binary and other dependencies in one convenient package. BIDS Apps run on all three major operating systems with no need for complex setup and configuration and thanks to the comprehensiveness richness of the BIDS standard they require little manual user input. Previous containerized data processing solutions were limited to single user environments and not compatible with most multi-tenant High Performance Computing systems. BIDS Apps overcome this limitation by taking advantage of the Singularity container technology. As a proof of concept, this work is accompanied by 22 ready to use BIDS Apps, packaging a diverse set of commonly used neuroimaging algorithms.\n\nAuthor SummaryMagnetic Resonance Imaging (MRI) is a non-invasive way to measure human brain structure and activity that has been used for over 25 years. There are thousands MRI studies performed every year generating a substantial amount of data. At the same time, many new data analysis methods are being developed every year. The potential of using new analysis methods on the variety of existing and newly acquired data is hindered by difficulties in software deployment and lack of support for standardized input data. Here we propose to use container technology to make deployment of a wide range of data analysis techniques easy. In addition, we adapt the existing data analysis tools to interface with data organized in a standardized way. We hope that this approach will enable researchers to access a wider range of methods when analyzing their data which will lead to accelerated progress in human neuroscience.

Neuroscience↗

bioRxiv2016

A phenome-wide examination of neural and cognitive function

This data descriptor outlines a shared neuroimaging dataset from the UCLA Consortium for Neuropsychiatric Phenomics, which focused on understanding the dimensional structure of memory and cognitive control (response inhibition) functions in both healthy individuals (138 subjects) and individuals with neuropsychiatric disorders including schizophrenia (58 subjects), bipolar disorder (49 subjects), and attention deficit/hyperactivity disorder (45 subjects). The dataset includes an extensive set of task-based fMRI assessments, resting fMRI, structural MRI, and high angular resolution diffusion MRI. The dataset is shared through the OpenfMRI project, and is formatted according to the Brain Imaging Data Structure (BIDS) standard.

Neuroscience↗

bioRxiv2016

Scanning the Horizon: challenges and solutions for neuroimaging research

Functional neuroimaging techniques have transformed our ability to probe the neurobiological basis of behaviour and are increasingly being applied by the wider neuroscience community. However, concerns have recently been raised that the conclusions drawn from some human neuroimaging studies are either spurious or not generalizable. Problems such as low statistical power, flexibility in data analysis, software errors, and lack of direct replication apply to many fields, but perhaps particularly to fMRI. Here we discuss these problems, outline current and suggested best practices, and describe how we think the field should evolve to produce the most meaningful answers to neuroscientific questions.

Scientific Communication and Education↗

bioRxiv2016

Power and sample size calculations for fMRI studies based on the prevalence of active peaks.

Mounting evidence over the last few years suggest that published neuroscience research suffer from low power, and especially for published fMRI experiments. Not only does low power decrease the chance of detecting a true effect, it also reduces the chance that a statistically significant result indicates a true effect (Ioannidis, 2005). Put another way, findings with the least power will be the least reproducible, and thus a (prospective) power analysis is a critical component of any paper. In this work we present a simple way to characterize the spatial signal in a fMRI study with just two parameters, and a direct way to estimate these two parameters based on an existing study. Specifically, using just (1) the proportion of the brain activated and (2) the average effect size in activated brain regions, we can produce closed form power calculations for given sample size, brain volume and smoothness. This procedure allows one to minimize the cost of an fMRI experiment, while preserving a predefined statistical power. The method is evaluated and illustrated using simulations and real neuroimaging data from the Human Connectome Project. The procedures presented in this paper are made publicly available in an online web-based toolbox available at www.neuropowertools.org.

Neuroscience↗

bioRxiv2016

A practical guide for improving transparency and reproducibility in neuroimaging research

Recent years have seen an increase in alarming signals regarding the lack of replicability in neuroscience, psychology, and other related fields. To avoid a widespread crisis in neuroimaging research and consequent loss of credibility in the public eye, we need to improve how we do science. This article aims to be a practical guide for researchers at any stage of their careers that will help them make their research more reproducible and transparent while minimizing the additional effort that this might require. The guide covers three major topics in open science (data, code, and publications) and offers practical advice as well as highlighting advantages of adopting more open research practices that go beyond improved transparency and reproducibility.

Neuroscience↗

bioRxiv2015

Retrieval-extinction within the memory reconsolidation window does not influence appetitive choice

Influencing choice behavior is key to achieving behavioral change. Traditional means to influence choice behavior rely on effortful self control, which is known to be fragile under several circumstances, rendering these methods ineffectual in maintaining any change in behavior over time. Behavioral maintenance efforts are likely more effective over the long term if they target more automatic processes such as attention or memory. Memories are not set in stone and are vulnerable to change and updating under certain circumstances when retrieved. It is possible to target specific memories for updating. In two studies, we sought to update the memory for an appetitive choice by way of reversal learning following retrieval of the targeted choice behavior. We found that targeting memories of a choice behavior for updating shortly after a reminder did not significantly attenuate the renewal of the targeted choice under extinction conditions. Possible explanations and suggested future directions are discussed.

Animal Behavior and Cognition↗