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BIRS 2016: Opening  the analysis black box: Improving robustness and interpretation BIRS 2016: Opening  the analysis black box: Improving robustness and interpretation

BIRS 2016: Opening the analysis black box: Improving robustness and interpretation - PowerPoint Presentation

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BIRS 2016: Opening the analysis black box: Improving robustness and interpretation - PPT Presentation

Matthew Brown PhD University of Alberta Canada Overview About us Preprocessing quality assurance Interpretation of group vs individual differences Trial type fMRI signatures Dept Psychiatry ID: 933213

model patients interpretation adhd patients model adhd interpretation controls group differences fmri individual brown 200 preprocessing 2012 response trial

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Slide1

BIRS 2016:Opening the analysis black box: Improving robustness and interpretation

Matthew Brown, PhD

University of Alberta, Canada

Slide2

OverviewAbout us

Preprocessing quality assurance

Interpretation of group vs. individual differences

Trial type fMRI signatures

Slide3

Dept. PsychiatryDept. Computing Science

Computational

Psychiatry

Group

Slide4

DiagnosisWhat disease?PrognosisPredict patient response to treatment options

Clinical decision-making

Slide5

What are we detecting?10 psychosis patients, 10 controls, fMRI

H

ighly diagnostic Fourier power distribution from voxels IN THE EYES

Eye movement disturbances in psychosis

Slide6

ADHD-200 and ABIDE datasetsn=1000 approx.

ADHD patients or autism patients

Structural MRI, resting state fMRI

Simple diagnosis

Classify patients vs. controls

A

ccuracy 50-70% in various papersSome papers reported higher 75%+ accuracy BUT cherry

-picking sites?

Slide7

ADHD-200 Global Competition

Best-performing algorithm, but did not win

Used only non-imaging features:

Age, gender, handedness, IQ, site of

scan

3

-class classification (ADHD-c, ADHD-

i

, control)

63

% hold-out accuracy (vs. 54% chance)

Using non-imaging features

Brown et al. 2012

Chance accuracy

Validation

Accuracy (%)

Slide8

Histogram of oriented gradient (HOG) features

Image from

Ghiassian

et al. under review.

Also see

Dalal

and

Triggs

2005. IEEE Computer Society Conference on. vol. 1.

IEEE

,

p

.886

–893.

Slide9

ADHD-200 and ABIDE datasetsGhiassian

et al. under review

State of the art (as of 1.5 years ago)

2-class classification

(patients

vs.

controls)

ADHD-200

ABIDE

Chance

55%

51%

Non-imaging

69%

60%

Non-imaging + Structural MRI

70%

64%

Non-imaging + Functional

MRI

64%

65%

Slide10

OverviewAbout us

Preprocessing quality assurance

Interpretation

of group vs. individual differences

Trial

type fMRI

signatures

Slide11

Registration failure

Subject 1

Subject 15

Fixed ->

Standard preprocessing methods

failed for 1 of 21 subjects.

Slide12

Inter-site variability

Sen

et al. in preparation

PCA Component 1

PCA Component 2

ADHD-200 Subjects Projected onto PCA component space

Each

colour

is a different scanning site.

Even

with standard normalization procedures, inter-site structure remains in the data.

Slide13

OverviewAbout us

Preprocessing quality assurance

Interpretation of group vs. individual differences

Trial type fMRI signatures

Slide14

Clinical research

Huntington’s

Image

from

Wikipedia

Healthy

One goal: Associate disease with biological features

Slide15

ADHD-200 resting state fMRI functional connectivity analysis

ICA

Brown et al. 2012

Slide16

ADHD patients vs. controls

“Default mode” network

Patients vs.

c

ontrols

Brown et al. 2012

“Desired” simple interpretation: “Patients are different from controls. This difference tells us something about the disease.”

Slide17

Group vs. individual differences

Patients

Controls

Statistically significant

group

differences, but substantial overlap between

individual

patients and controls.

Brown et al. 2012

Slide18

InterpretationSimple interpretation “patients are different from controls”

Overlap precludes simple interpretation

Yet many papers provide precisely and only the simple interpretation

Patients

Controls

Brown et al. 2012

Slide19

OverviewAbout us

Preprocessing quality assurance

Interpretation of group vs. individual differences

Trial type fMRI signatures

Slide20

Black box analysis

Analysis

Software

Slide21

General linear model regression

Model voxel i’s

timecourse

Model matrix for trial type k

Slide22

Two different models for hemodynamic response function

SPM canonical

model

Finite

impulse

r

esponse

m

odel

Slide23

Check

deconvolved

timecourses

Basically agree

on

shape (

but not statistical differences in this case)

SPM canonical model

Finite impulse response

model, same region

Slide24

Check

d

econvolved

timecourses

SPM canonical model

Finite impulse response

model, same region

Noise

in

deconvolved

timecourses

Slide25

Another example

SPM canonical model

Finite impulse response

model, same region

Noise in

deconvolved

timecourses

Slide26

GLM analysisCheck deconvolved

timecourses

What is the model fitting

Noise vs. signal

Model selection

regularization

Slide27

SummaryQuality check everything

Visualization

Intermediate steps and final

results

Particularly important for non-technical end-users

Slide28

AcknowledgementsPeople: Azad, Benoit, Dursun

,

Ghiassian

,

Greenshaw

, Greiner,

Juhas, Purdon, Ramasubbu, Rish

, Sen, SilverstoneFunding: AICML, AIHS, CIHR, Norlien

Foundation, AHS, AMHB,

UAlberta

Questions?

Slide29

InvitationContinue informing other researchers about analysis pitfalls and caveats.

Questions?

Slide30

Title