scieee Science in your language
[de] (orig)

Brain lesion segmentation using Convolutional Neuronal Networks

Abstract

Convolutional neural networks (CNN) are powerful tools for learning representations from im-ages. They are being used in a large range of applications, being the state-of-the art in manycomputer vision tasks. In this work, we study the brain tumor segmentation problem using CNNs and the publicly available BraTS dataset. One of the key factors for this task is which training scheme is used since it should deal with memory constraints and should alleviate the high-imbalance nature between healthy and lesion tissue in the brain. Thus, the purpose of this project is to propose a comparison between several training schemes and extensively analyze and evaluate them in terms of the dice score. We evaluate dense-training against patch-sampling, and particularly, fixed-rule against adaptive sampling scheme. Furthermore, variants and modifications of the existing training schemes have been proposed in order to enhance their performance. Finally, several loss functions for each training scheme have been analyzed.

Read accessible full text

Brain lesion segmentation using Convolutional Neuronal Networks

Author: Bonnín Rosselló, Clara
Publisher: Universitat Politècnica de Catalunya
Year: 2018
Source: https://upcommons.upc.edu/bitstream/2117/117984/1/FinalThesis_ClaraBonninRossello.pdf
UNIVERSITAT POLIT`
ECNICA DE CATALUNYA
B ain lesion segmen a ion using
Con olu ional Neu onal Ne wo ks
by
Cla a Bonn´ın Rossell´o
In pa ial ul ilmen o he equi emen s o he deg ee in
Ci`encies i Tecnologies de Telecomunicaci´o enginee ing
in he
Escola T`ecnica d’Enginye ia de Telecomunicaci´o de Ba celona
Image P ocessing G oup
Ad iso s: Ve ´onica Vilaplana and Ad i`a Casami jana
May 2018
UNIVERSITAT POLIT`
ECNICA DE CATALUNYA
Abs ac
Escola T`ecnica d’Enginye ia de Telecomunicaci´o de Ba celona
Image P ocessing G oup
by Cla a Bonn´ın Rossell´o
Con olu ional neu al ne wo ks (CNN) a e powe ul ools o lea ning ep esen a ions om im-
ages. They a e being used in a la ge ange o applica ions, being he s a e-o - he a in many
compu e ision asks. In his wo k, we s udy he b ain umo segmen a ion p oblem using
CNNs and he publicly a ailable B aTS da ase . One o he key ac o s o his ask is which
aining scheme is used since i should deal wi h memo y cons ain s and should alle ia e he
high-imbalance na u e be ween heal hy and lesion issue in he b ain.
Thus, he pu pose o his p ojec is o p opose a compa ison be ween se e al aining schemes
and ex ensi ely analyze and e alua e hem in e ms o he dice sco e. We e alua e dense-
aining agains pa ch-sampling, and pa icula ly, ixed- ule agains adap i e sampling scheme.
Fu he mo e, a ian s and modi ica ions o he exis ing aining schemes ha e been p oposed in
o de o enhance hei pe o mance. Finally, se e al loss unc ions o each aining scheme ha e
been analyzed.
Acknowledgemen s
I would like o exp ess my since e g a i ude o se e al people. Fi s ly, I would like o hank
specially Ad i`a Casami jana and Ve ´onica Vilaplana, he supe iso s o his hesis, o hei
ad ice and pa ience du ing he whole p ojec and o gi ing me he chance o lea n deep lea ning
in his challenging wo k ha combines biomedicine and enginee ing. O cou se, I would like o
hank o he collabo a ion schola ship ecei ed o ealize his hesis. I would like o ake his
oppo uni y o hank he ETSETB eache s and also my colleges o his las wonde ul 4 yea s
in he UPC. Finally, I would like o dedica e his p ojec o my amily and o `
0sca , o hei
suppo and unde s anding.
ii
Con en s
Abs ac i
Acknowledgemen s ii
Lis o Figu es
Lis o Tables ii
Abb e ia ions iii
Symbols ix
1 In oduc ion 1
1.1 S a emen o Pu pose ................................. 1
1.2 Ou line o he wo k ................................... 3
1.3 Technical Rema ks ................................... 3
2 S a e o he a 4
3 Me hodology 6
3.1 Sys em A chi ec u e .................................. 6
3.1.1 A chi ec u e .................................. 6
3.1.1.1 Masked V-NET ........................... 6
3.1.1.2 Deep Medic Ne wo k ........................ 6
3.1.2 Loss unc ions ................................. 8
3.1.2.1 C oss-en opy ............................ 8
3.1.2.2 Dice Simila i y Coe icien ..................... 8
3.1.2.3 Gene alised Dice Sco e ....................... 10
3.1.2.4 Weigh ed loss ............................. 10
3.1.3 Me ics ..................................... 10
3.1.3.1 Dice Sco e .............................. 10
3.1.3.2 Con usion ma ix .......................... 11
3.2 T aining scheme .................................... 11
3.2.1 Dense- aining ................................. 11
3.2.2 Pa ch sampling ................................. 11
3.2.2.1 Baseline: Fo eg ound-backg ound ................. 11
3.2.2.2 Pe -Class sampling scheme ..................... 12
3.2.2.3 Cu iculum Adap i e Sampling ................... 12
3.2.2.4 Baseline Adap i e Sampling Scheme ................ 13
iii
Con en s i
4 Expe imen s and Resul s 14
4.1 Da ase ......................................... 14
4.2 Dense- aining ..................................... 15
4.3 Pa ch sampling ..................................... 16
4.3.1 Fixed- ule sampling schemes ......................... 16
4.3.1.1 Loss unc ion: c oss-en opy .................... 17
4.3.1.2 Loss unc ion: weigh ed c oss-en opy ............... 18
4.3.2 Adap i e sampling schemes .......................... 19
4.3.2.1 CASED ................................ 20
4.3.2.2 BaseASS ............................... 22
4.4 Discussion ........................................ 25
5 Budge 28
6 Conclusions and u u e de elopmen 29
A Code o he p ojec 31
B Dense- aining 32
B.1 Se up .......................................... 32
B.2 T aining Cu es ..................................... 32
C Pa ch sampling 34
C.1 Se up .......................................... 34
C.2 T aining Cu es ..................................... 34
Bibliog aphy 37

Lis o Figu es
1.1 MRI T1 ......................................... 2
1.2 MRI T1c ........................................ 2
1.3 MRI T2 ......................................... 2
1.4 MRI FLAIR ....................................... 2
1.5 Mul imodal MRI images om subjec B a s17 −CBICA −ALX ........ 2
1.6 Glioma sub- egion. .................................. 2
3.1 V-Ne .......................................... 7
3.2 Two-pa h Deep Medic a chi ec u e .......................... 9
3.3 Example o eal s cap u ed dis ibu ion in he aining da a o BRATS 2015 . . 12
3.4 Schema ic diag am o CASED amewo k ...................... 13
4.1 Loss unc ion con e gence o dense- aining ..................... 16
4.2 G ound T u h s P edic ion o subjec B a s17 −T CIA −444 −1....... 16
4.3 Dice Whole o eg ound-backg ound .......................... 18
4.4 Dice Co e o eg ound-backg ound ........................... 18
4.5 Dice Enhance o eg ound-backg ound ........................ 18
4.6 T aining / Valida ion Dice Sco e E olu ion o baseline o eg ound-backg ound . 18
4.7 Dice Whole Pe -Class sampling scheme ........................ 18
4.8 Dice Co e Pe -Class sampling scheme ......................... 18
4.9 Dice Enhance Pe -Class sampling scheme ...................... 18
4.10 T aining / Valida ion Dice Sco e E olu ion o Pe -Class sampling scheme . . . . 18
4.11 Dice Whole pe o eg ound-backg ound ....................... 19
4.12 Dice Co e pe o eg ound-backg ound ........................ 19
4.13 Dice Enhance pe o eg ound-backg ound ...................... 19
4.14 T aining / Valida ion Dice Sco e E olu ion o o eg ound-backg ound sampling
scheme and weigh ed loss ............................... 19
4.15 Dice Whole Pe -Class sampling scheme ........................ 19
4.16 Dice Co e Pe -Class sampling scheme ......................... 19
4.17 Dice Enhance Pe -Class sampling scheme ...................... 19
4.18 T aining / Valida ion Dice Sco e E olu ion o Pe -Class sampling scheme and
weigh ed loss ...................................... 19
4.19 Pa ch dis ibu ion e olu ion du ing aining in baseline CASED model ...... 21
4.20 Pa ch dis ibu ion e olu ion du ing aining in slowed down model ........ 21
4.21 Valida ion Dice Whole CASED ............................ 22
4.22 Valida ion Dice Co e CASED ............................. 22
4.23 Valida ion Dice Enhance CASED ........................... 22
4.24 Tes DSC o all h ee CASED a ian s ....................... 22
4.25 Valida ion Dice Whole BaseASS ........................... 23
4.26 Valida ion Dice Co e BaseASS ............................ 23
4.27 Valida ion Dice Enhance BaseASS .......................... 23
4.28 Tes DSC o all h ee BaseASS a ian s ....................... 23
4.29 Pa ch dis ibu ion e olu ion o he BaseASS model ................ 24
Lis o Figu es i
4.30 Pe cen age o class oxels pe ba ch pe epoch o BaseASS ............ 24
4.31 E o maps om subjec B a s17 −CBICA −AAL wi h BaseASS ........ 25
4.32 O e all Dice Whole Tumo Compa ison. Valida ion is done using he whole sub-
jec as inpu . ...................................... 26
4.33 O e all Dice Co e Tumo Compa ison. Valida ion is done using he whole subjec
as inpu . ......................................... 27
4.34 O e all Dice Enhance Tumo Compa ison. Valida ion is done using he whole
subjec as inpu . .................................... 27
B.1 Dice Whole ....................................... 32
B.2 Dice Co e ........................................ 32
B.3 Dice Enhance ...................................... 32
B.4 Dice Sco e E olu ion o c oss-en opy loss unc ion ................. 32
B.5 Dice Whole ....................................... 33
B.6 Dice Co e ........................................ 33
B.7 Dice Enhance ...................................... 33
B.8 Dice Sco e E olu ion o DSC loss unc ion ..................... 33
C.1 Dice Whole ....................................... 35
C.2 Dice Co e ........................................ 35
C.3 Dice Enhance ...................................... 35
C.4 Dice Sco e E olu ion o he baseline CASED model ................ 35
C.5 Dice Whole ....................................... 35
C.6 Dice Co e ........................................ 35
C.7 Dice Enhance ...................................... 35
C.8 Dice Sco e E olu ion o he al e ed dis ibu ion CASED model .......... 35
C.9 Dice Whole ....................................... 35
C.10 Dice Co e ........................................ 35
C.11 Dice Enhance ...................................... 35
C.12 Dice Sco e E olu ion o he slowed down dis ibu ion CASED model ...... 35
C.13 Dice Whole ....................................... 35
C.14 Dice Co e ........................................ 35
C.15 Dice Enhance ...................................... 35
C.16 Dice Sco e E olu ion o BaseASS model ....................... 35
C.17 Dice Whole ....................................... 36
C.18 Dice Co e ........................................ 36
C.19 Dice Enhance ...................................... 36
C.20 Dice Sco e E olu ion o BaseASS model and median e o ............ 36
C.21 Dice Whole ....................................... 36
C.22 Dice Co e ........................................ 36
C.23 Dice Enhance ...................................... 36
C.24 Dice Sco e E olu ion o BaseASS and gene alised DSC .............. 36
C.25 Tes DSC o BaseASS and Deep Medic ne wo k .................. 36
Lis o Tables
3.1 Con usion Ma ix Example .............................. 11
4.1 Compa ison o mean alida ion DSC me ics o dense- aining .......... 15
4.2 Con usion ma ix o whole subje using DSC cos unc ion ( alida ion) ..... 15
4.3 Compa ison o mean alida ion DSC me ics o ixed- ule sampling schemes . . 17
4.4 Con usion ma ix o baseline o eg ound-backg ound ( alida ion) ........ 17
4.5 Con usion ma ix Pe -Class sampling scheme ( alida ion) ............. 18
4.6 Con usion ma ix o o eg ound-backg ound sampling using weigh ed loss ( ali-
da ion) ......................................... 19
4.7 Con usion ma ix Pe -Class sampling scheme using weigh ed loss ( alida ion) . . 19
4.8 Compa ison o mean alida ion DSC me ics o CASED .............. 20
4.9 Con usion ma ix baseline CASED scheme ( alida ion) .............. 20
4.10 Con usion ma ix slowed down CASED scheme ( alida ion) ............ 21
4.11 Compa ison o mean alida ion DSC me ics o BaseASS ............. 23
4.12 Con usion ma ix BaseASS wi h c oss-en opy loss ( alida ion) .......... 25
4.13 Con usion ma ix BaseASS wi h Gene alised DSC loss ( alida ion) ........ 25
4.14 Con usion ma ix o BaseASS and Deep Medic ne wo k ( alida ion) ....... 25
4.15 Mean Dice sco e me ics om he main expe imen s ca ied on .......... 26
5.1 P ojec Budge ..................................... 28
6.1 Compa ison be ween ou app oach and some o 2017 MICCAI B aTS Challenge 30
ii
Abb e ia ions
BaseASS Baseline Adap i e Sampling Scheme
CNN Con olu ional Neu al Ne wo k
CASED Cu iculum Adap i e Sampling o Ex eme Da a Imbalance
DSC Dice Simila i y Coe icien
FLAIR Fluid A enua ed In e sion Reco e y
HGG High G ade Glioma
ROI Region O In e es
LGG Low G ade Glioma
MRI Magne ic Resonance Imaging
WL Weigh ed Loss
iii
Me hodology 5
he eme gence o di e en sampling schemes (dense- aining, pa chwise aining, e c..) and cos
unc ions.
Pe o mance o CNN is signi ican ly in luenced by he s a egy o ex ac ing aining samples. A
common app oach is selec ing image pa ches equally sampled om each class. Ano he app oach
is o equally sample backg ound and o eg ound segmen s. On he o he hand, by employing
dense- aining o by sampling pa ches uni o mly, i migh su e om se e e class imbalance.
Hence, mul iple cos unc ions ha e been p oposed o alle ia e his issue.
The loss unc ion p oposed is c oss-en opy. Howe e , when he aining da a is se e ely unbal-
anced, his o mula ion can lead o a s ongly biased es ima ion owa ds he majo i y class. A
weigh ed c oss-en opy (B osch e al. [19]) is p oposed o ackle his p oblem, whe e he weigh s
a e in e sely p opo ional o he class equencies. Also, a di e en iable e sion o he Dice Sco e
Coe icien (DSC), p oposed by Mille a i e al. [20], is used as loss unc ion as i measu es he
o e lap o he egion o in e es (ROI). Recen ly, wo no el loss unc ions ha e been p esen ed:
he Gene alised DSC [21] and he Wasse s ein Dice .
This wo k ocuses on he segmen a ion o b ain umo s ollowing he guidelines indica ed by
B aTS Challenge, which began in 2012. The me hods submi ed in hese las yea s can be ound
in [17], [22]. The MICCAI (The Medical Image Compu ing and Compu e Assis ed In e en ion
Socie y) B aTS Challenge has an upda ed leade boa d1o he models wi h he bes pe o mances
acco ding o ollowing me ics: Dice sco e, sensi i i y, speci ici y and Hausdo dis ance. UCL-
TIG is in he i s posi ion on he anking wi h Ensembles o Mul iple Models and A chi ec u es
o Robus B ain Tumou Segmen a ion [18]. I achie es a dice whole umo o 0.90499, a dice
co e umo o 0.83779 and and a dice enhancing umo o 0.78585.
1h ps://www.cbica.upenn.edu/B aTS17/lboa dValida ion.h ml

Chap e 3
Me hodology
3.1 Sys em A chi ec u e
3.1.1 A chi ec u e
Two di e en a chi ec u es ha e been s udied in o de o disce n which one combined wi h o he
con igu a ions has he bes beha io : The Masked V-Ne [12] and he Deep Medic [11].
3.1.1.1 Masked V-NET
The masked V-Ne [12] is a modi ied e sion o he V-Ne a chi ec u e [20], which consis s o a
downsampling o encode pa h in cha ge o compac ing he signal and an upsampling o decode
pa h ha combines coa se ea u es om he encode ou pu wi h ine ea u es om hidden, in-
e media e le els o he encode o p o ide a segmen ed image o he same esolu ion as he inpu
image. The modi ica ions include he use o small ke nels o size 33, ba ch no maliza ion a e he
con olu ion and hen ReLU as non-linea i y. I was also in oduced a modi ied exp ession o he
esidual connec ions ha aim o p ese e he inpu signal h ough all he ne wo k. Max-pooling,
epea ed up-sampling o spa ial co espondence and 1x1x1 con olu ion a e a ian s in oduced
o ensu e dimensions ma ched in he addi ion laye . No e ha he ROI mask in oduced be o e
he inal p edic ions was only used o he dense- aining expe imen s. See igu e 3.1.
3.1.1.2 Deep Medic Ne wo k
The Deep Medic a chi ec u e p oposed in [11] consis s in cap u ing con ex ual and spacial in-
o ma ion h ough wo pa allel pa hs wi h di e en ea u e esolu ion ha sa es compu a ional
cos s and a oids pooling which could a ec on he accu acy o ou sys em. The 11-laye a chi ec-
u e p oposed by Deep Medic [11] is buil as shown in igu e 3.2. A high esolu ion pa h is able
o cap u e he mos complex de ails wi hin a small local neighbou hood, while a pa allel low
esolu ion pa h cap u es image-le el ea u es such as localiza ion o umo size. The di e ence in
6
Me hodology 7
Figu e 3.1: V-Ne
Me hodology 8
esolu ion is achie ed wi h di e en ecep i e ields: bo h pa hs a e buil upon a conca ena ion
o con olu ional laye s bu he la e has a pooling module a he e y beginning.
The ke nels on he con olu ional laye s o bo h high and low esolu ion pa hs a e o size 33. The
esul ing ma ices o he con olu ional laye s a e i s combined in o wo ull classi ica ion laye s
and hen inally classi ied.
3.1.2 Loss unc ions
Di e en loss unc ions ha e been conside ed in o de o s udy which one i s be e o ou
segmen a ion p oblem. The h ee cos unc ions ha will be s udied a e: c oss-en opy, Dice
Simila i y Coe icien (DSC) and Gene alised DSC.
3.1.2.1 C oss-en opy
C oss-en opy loss [23] o a mul i-class se ing can be exp essed as ollows
L(ˆy, y) = −
N
X
n=1
ynlog( ˆyn) (3.1)
No e ha Ns ands o he numbe o classes and yand ˆya e N-dimensional ec o s, whe e
yna e he ue labels o he class nand ˆyna e he so max ou pu s o he ne wo k o hose
ue labels. The mean c oss-en opy o e he whole ba ch is used as he cos unc ion a each
i e a ion and is compu ed as ollows:
¯
L(ˆy, y) = −1
|Y|X
y
X
n
ynlog( ˆyn) (3.2)
whe e Y e e s o aining samples om he ba ch.
3.1.2.2 Dice Simila i y Coe icien
Dice Sco e o mul i-class segmen a ion [24] is a measu e o simila i y be ween wo bina y se s:
he g ound u h G and he p edic ion P. Each se consis s o a egion o in e es (ROI) and
backg ound and he dice sco e, D[0,1], is he a io be ween he in e sec ion o he g ound- u h
and p edic ion ROIs and he sum o he a eas o bo h ROIs. The ollowing exp ession explains
he idea behind his loss unc ion.
D=2|P∩G|
|G|+|P|(3.3)
Then, a con inuous and di e en ial app oxima ion can be done by using so max p edic ions in-
s ead o he p edic ions hemsel es. The esul o a e aging and adap ing he p e ious exp ession
Me hodology 9
Figu e 3.2: Two-pa h Deep Medic a chi ec u e
Me hodology 10
o ou mul i-class p oblem is as ollows
¯
L(ˆy, y) = 1
|N|X
nN
2Piyi
nˆ
yi
n
Pi(yi
n+ˆ
yi
n)(3.4)
3.1.2.3 Gene alised Dice Sco e
The gene alised Dice Sco e is p oposed as loss unc ion in [21]. I s a modi ied e sion o he DSC
and is gi en by:
¯
L(ˆy, y)=1−2PN
n=1 αnPiyi
nˆ
yi
n
PN
n=1 αnPi(yi
n+ˆ
yi
n)(3.5)
whe e αnis a weigh o balance he impac in he loss unc ion o class n. Weigh ing by he
in e se o he class’ olume co ec s he con ibu ion o each label and educes he co ela ion
be ween he egion size and he Dice sco e. I is calcula ed as he in e se o he squa ed sum o
all he oxels o class n:
αn=1
(Piyi
n)2
3.1.2.4 Weigh ed loss
To u he elimina e he nega i e impac o he class imbalance, a weigh ed loss Lwis p oposed
as ollows. Whe e Lnis he speci ic loss o a ce ain class nN and kαnkis he he p obabili y
o appea ance o ha ce ain class. The e o e, by in e ing his p obabili y, we manage o gi e
mo e weigh o classes ha appea much less equen ly han o he s.
Lw=X
nN
1
αn
Ln(3.6)
The class equency αnis calcula ed as he sum o all he oxels o class n di ided by he sum
o all he oxels o he N classes:
αn=Piyi
n
PN
n=1 Piyi
n
(3.7)
3.1.3 Me ics
The me ics used o e alua e he pe o mance o each o he expe imen s ca ied on a e de ailed
below.
3.1.3.1 Dice Sco e
The e alua ion o he me hod using he dice sco e was calcula ed acco ding o 3.4 o di e en
ROI de ini ions: umo co e (classes 1 and 3), whole umo (classes 1,2,3) and enhancing umo
(class 3). This e alua ion amewo k is imposed by he Mul imodal B ain Tumo Segmen a ion
Challenge [3].

Me hodology 11
3.1.3.2 Con usion ma ix
The con usion ma ix is a able which allows o e alua e i ou segmen a ion sys em is mislabelling
one class as ano he . Each ow o he able ep esen s he ue class and each column he
p edic ed class. This able is use ul o gi e an idea o which classes a e well classi ied and which
a e w ongly con used wi h he o he s. I gi es us insigh s o how a model can be imp o ed. The
con usion ma ices in his documen will p esen he ollowing s uc u e:
G P 0 1 2 3
0
1
2
3
Table 3.1: Con usion Ma ix Example
3.2 T aining scheme
3.2.1 Dense- aining
Be o e analyzing how we explo e he pa ch wise aining scheme, which is he main con ibu ion
o ou wo k, we s udy dense- aining. We denomina e dense- aining he s a egy ha uses he
whole MRI image and he ou modali ies as inpu in o he ou Con olu ional Neu al Ne wo k.
The pe o mance o his aining scheme will be analyzed o wo di e en loss unc ions.
3.2.2 Pa ch sampling
Pa ch-sampling aining scheme consis s o eeding he ne wo k wi h small h ee-dimensional
pa ches o each subjec . Each o hese slices is associa ed wi h 4 di e en modali ies: T1,
T2, T1C and FLAIR and i s size is se o 643. The sampling scheme can be c i ique o any
medical applica ion and an exhaus i e analysis o di e en me hods is pe o med h oughou
he manusc ip wi h u he nume ical compa ison. In he case o b ain umo segmen a ion,
he high imbalance be ween backg ound and umo egions and sub egions may equi e lexible
me hod ha balances he inpu aining dis ibu ion o he di e en classes.
3.2.2.1 Baseline: Fo eg ound-backg ound
The aining scheme used in [11] ies o sol e he imbalance p oblem by a sampling scheme ha
samples he cen al- oxel o each pa ch wi h equip obabili y be ween o eg ound ( umo egions)
and backg ound. Hence, each ba ch is build by he same numbe o pa ches whose cen al oxel
is o eg ound and backg ound. No e ha no dis inc ion is made be ween umo sub egions. This
is o main ain he ela i e dis ibu ion o he o eg ound classes and a he same ime accoun
o he imbalance p oblem be ween heal hy issue and umo issue.
Me hodology 12
Figu e 3.3 om [11] shows how he ela i e dis ibu ion o he o eg ound classes is closely
p ese ed and he imbalance in compa ison o he heal hy issue is au oma ically alle ia ed.
Figu e 3.3: Example o eal s cap u ed dis ibu ion in he aining da a o BRATS 2015
This o eg ound-backg ound sampling scheme has been selec ed o be ou baseline scheme on
pa ch sampling.
3.2.2.2 Pe -Class sampling scheme
This aining scheme p oposes sampling pa ches acco ding o a ule ha ensu es equip obabili y
be ween all classes in he cen al- oxel a each epoch. The idea is o accoun o he imbalance
be ween backg ound and each one o he umo sub egions. I al e s he balance be ween each
class and hence, i cap u es a a he di e en dis ibu ion om he o iginal.
3.2.2.3 Cu iculum Adap i e Sampling
Cu iculum Adap i e Sampling (CASED) [25] scheme i s ’s objec i e is o ackle he p oblem
o class imbalance. The basic ideas o his sys em a e:
1. Lea n ea u es ela ed o umo : s a in oducing only pa ches wi h umo in o he ne -
wo k.
2. As he ne wo k is aining, s a adding backg ound pa ches o lea n heal hy issue p op-
e ies.
3. In he end, uni o m sampling is eached o mimic eal da a dis ibu ion.
CASED scheme can be di ided in wo pa s: Cu iculum and Adap i e Sampling.
Cu iculum is he pa ha ackles he class imbalance p oblem con olling he inpu pa ches o
he ne wo k by deciding be ween umo -sampling and uni o m-sampling gene a o s. I aining
was pe o med using only umo pa hces, i could esul in o e i ing because i would no lea n
how o ep esen he main pa o he MRI image, he backg ound class. Then, he cu iculum
pa is esponsible o dec easing (as unc ion o he aining examples seen) he numbe o pa ches
wi h umo un il i eaches he eal dis ibu ion. The h eshold pxis gi en by Equa ion 3.8. Fo
alues g ea e han px umo pa ches a e selec ed, o he wise i is picked any andom pa ch.
px+1 =px∗1
M
(i e ∗epochs∗K)−1
(3.8)
Expe imen s and Resul s 13
wi h
p0= 1
whe e Mis he numbe o segmen s, i e he numbe o i e a ions, epochs he o al numbe o
aining epochs and Kis a cons an o speed up o slow down he h eshold cu e.
Adap i e Sampling is equi ed o e ine he p e ious pa . E en using he cu iculum, solu ions
wi h alse posi i es would s ill happen. Mo eo e , mos ly all oxels on b ain images could be
con iden ly classi ied as backg ound. The e o e, he adap i e sampling encou ages aining inpu s
whose p edic ions a e alse posi i es.
Figu e 3.4: Schema ic diag am o CASED amewo k
3.2.2.4 Baseline Adap i e Sampling Scheme
Adap i e Sampling Scheme o E icien ly T ain Fully Con olu ional Ne wo ks [26], om now
on BaseASS (baseline adap i e sampling scheme), sugges s a pa chwise aining scheme ha
p e ends o adap i ely build aning samples a each epoch by looking a he ne wo k aining
e o . Fo each subjec , e o maps Eia e build concu en ly a he end o each epoch as:
Ei= 1 −CNN(w, In(x))Ln(x)(3.9)
whe e CNN(w, In(x))Ln(x) ep esen s he so max p edic ions calcula ed using he aining
weigh s wo e an image In. Thus, a pa ch is accep ed in o he ba ch acco ding o i s ela-
ion o he h eshold de ined by:
Ei(c)> U(0,1) −(3.10)
whe e c is he cen al oxel o he pa ch, U(0,1) is a andom uni o m a iable and a pa ame e
o calib a e he algo i hm: = 0 means a comple ely adap i e scheme and = 1 he uni o m
sampling scheme.
Chap e 4
Expe imen s and Resul s
This chap e p esen s and compa es he esul s ob ained om applying he me hodologies men-
ioned in Chap e 3.
4.1 Da ase
In his hesis, he da a used o ain he ne wo k has been ob ained om he MICCAI B aTS
2017 Challenge [3]. This da ase is composed by 210 HGG (high g ade glioma) and 75 LGG (low
g ade glioma) subjec s o which 171 a e used o aining (60%) and 116 a e used o alida ion
pu poses (40%). No da a augmen a ion was used in any expe imen . The ou modali ies o each
MRI image (na i e T1, pos -con as T1-weigh ed, T2-weigh ed and T2 FLAIR) a e co- egis e ed
o he same ana omical empla e and in e pola ed o he same esolu ion (1 mm3).
T aining he ne wo k elies on he p ope selec ion o hype pa ame e s, a w ong choice can lead
o o e i ing, unde i ing o simply no aining. Each expe imen should ha e been op imized
indi idually un il ob aining he bes esul s. Besides he ac ha his is oo compu a ionally
demanding, we ha e no done his in o de o be able o compa e all he models unde he same
condi ions. Fi s , he lea ning a e, which ells he op imize how a has o mo e he weigh s in
he di ec ion o he g adien , was se o 0.0005. The momen um was se o 0.99. Regula iza ion
p e en s he coe icien s o o e i and i depends on wo a iables: L2 is a ac o mul iplying
he sum o he squa e o he weigh s, while L1 is he ac o mul iplying he absolu e sum o
he weigh s. The alues chosen we e L1=0.00001, L2=0.005. The numbe o aining epochs is
a iable o each expe imen . Masked V-Ne was used as he base a chi ec u e o all expe imen s
excep one, whe e Deep Medic Ne wo k was used. The ini ializa ion o he weigh s was done
acco ding o [27].
Fo pa ch sampling, we used 600 segmen s/epoch o aining and 400 segmen s/epoch o ali-
da ion wi h a ba ch size o 10.
14
Expe imen s and Resul s 21
G P % 0 1 2 3
0 0,99877 0,00016 0,00095 0,00012
10,10293 0,57165 0,24711 0,07831
20,15830 0,04181 0,78414 0,01576
30,05627 0,04030 0,06982 0,83361
Table 4.10: Con usion ma ix slowed down CASED scheme ( alida ion)
aking in o accoun he cen al oxel o decide which pa ch ype is i . I we conside ed all he
pa ch, calcula ing he class wi h maximum p esence we would always ob ain class 0. The hi d
plo is he cu iculum cu e om equa ion 3.8. O e all, he slowed down e sion was ound o
ha e he bes pe o mance.
Figu e 4.19: Pa ch dis ibu ion e olu ion du ing aining in baseline CASED model
Figu e 4.20: Pa ch dis ibu ion e olu ion du ing aining in slowed down model

Expe imen s and Resul s 22
Finally, he model was used o in e he es da a segmen a ion. Boxplo s om igu e 4.24
show he compa ison in DSC ac oss he h ee models. The ou lie s had been checked and we e
mainly due o MRI inpu images om he da ase wi h poo condi ions. In conclusion, a ian
2 demons a es o be be e han baseline CASED o only including a ian 1 acco ding o
he mean DSC me ics, he con usion ma ix and he alida ion boxplo s. Un il his poin , his
esul ou pe o ms all he o he schemes used p e iously. This is because in he las i e a ions he
aining dis ibu ion app oaches he ue dis ibu ion and he e o e ge s a be e gene aliza ion.
Figu e 4.21: Val-
ida ion Dice Whole
CASED
Figu e 4.22: Valida-
ion Dice Co e CASED
Figu e 4.23: Vali-
da ion Dice Enhance
CASED
Figu e 4.24: Tes DSC o all h ee CASED a ian s. F om le o igh : Baseline CASED,
modi ied sub egion dis ibu ion and slowed down CASED. Valida ion is done using he whole
subjec as inpu .
4.3.2.2 BaseASS
The baseline adap i e sampling scheme was implemen ed as men ioned in Chap e 3. The base-
line me hod uses c oss-en opy and he cen al oxel e o as he c i e ia o selec ion. Mo eo e ,
we explo e his model and p opose h ee al e na i es: 1) pa ch selec ion acco ding he median
e o alue o he whole pa ch (Eq. 4.1) ins ead o only he e o alue o he cen al oxel (Eq.
3.10); 2) use he Gene alised DSC loss unc ion ins ead o c oss-en opy; 3) use ano he a chi ec-
u e: Deep Medic ne wo k ins ead o masked V-Ne . Fo his las expe imen , he cos unc ion
chosen was c oss-en opy as i had shown o pe o m be e in his con igu a ion. This classical
a chi ec u e was chosen because, unlike Masked V-Ne [12], i does no ha e any max-pooling
laye . We wan o a oid max-pooling beacuse i educes he spa ial size o he ep esen a ion and
he eby i educes he numbe o aining pa ame e s, which migh con ain ele an in o ma ion
o ou segmen a ion ask.
median(Eipa ch )> U(0,1) −(4.1)
To be as ai as possible when compa ing, he es o pa ame e s emained ixed. We ained
baseline and he i s wo models wi h Adam Op imiza ion me hod [28] wi h a lea ning a e o
0.0005. The hi d model (Deep Medic Ne wo k) was ained using RMSp op op imize and a
lea ning a e o 0.0001. Fo mo e de ails consul he annex.
The esul s epo ed on Table 4.11 show ha BaseASS wi h classical c oss-en opy loss ou pe -
o ms Gene alised DSC. Howe e , BaseASS using he cen al oxel’s e o o he median e o
Expe imen s and Resul s 23
Scheme Dice Whole Dice Co e Dice Enhance
BaseASS 0,86286 0,74418 0,67466
BaseASS + Gene alised DSC 0,81759 0,69727 0,65100
BaseASS + Median e o as selec ion
c i e ia
0,85087 0,75052 0,657198
BaseASS + Deep Medic ne wo k 0,65379 0,55027 0,48243
Table 4.11: Compa ison o mean alida ion DSC me ics o BaseASS
o he pa ch show simila pe o mance. This sugges s ha using only he cen al oxel is enough
o ge a gene al ep esen a ion o he pa ch e o . This esul s can be clea ly con i med when
looking a he boxplo compa ison in Figu e 4.28. Finally, he masked V-Ne ne wo k ob ains
be e esul s han he Deep Medic Ne wo k. Ne e heless, he la e hype -pa ame e s had no
been op imized and we can’ conclude ha i is beha ing wo se ye . The las expe imen was
no wo h o be included in he boxplo compa ison 4.28, bu can be ound in he Appendix in
Figu e C.25.
Figu e 4.25: Val-
ida ion Dice Whole
BaseASS
Figu e 4.26: Val-
ida ion Dice Co e
BaseASS
Figu e 4.27: Vali-
da ion Dice Enhance
BaseASS
Figu e 4.28: Tes DSC o all h ee BaseASS a ian s. F om le o igh : BaseASS using
c oss en opy loss, BaseASS using median e o and BaseASS using gene alised DSC loss.
Valida ion is done using he whole subjec as inpu
Figu e 4.29 shows he numbe o segmen s o each class pe aining epoch o he BaseASS
model. Fo cla i ica ion, i is conside ed ha he pa ch class is de ined as he class o he cen al
oxel ( he one whose e o alue is aken as selec ion c i e ia). In compa ison o CASED scheme,
sec ion 4.3.2.1 (Figu e 4.19), he e he numbe o lesion pa ches is no educed in each epoch bu
emains cons an o all he aining. In con as , he numbe o backg ound pa ches dec eases
in each i e a ion. I can be seen ha he po ion o class 1 pa ches is sligh ly highe han ha
o class 2 and 3. This leads us o belie e ha i is a wise decision o gi e a li le mo e weigh o
class 1 han 2 o 3.
While Figu e 4.30 shows he aining dis ibu ion o he ba ch in each i e a ion. I can be
obse ed ha despi e o choosing di e en numbe o segmen s o each class, he aining dis-
ibu ion emains almos cons an o all he epochs. Mo eo e , his dis ibu ion is close o he
eal one.
Quali a i e esul s o he e o maps calcula ed in each i e a ion (Figu e 4.31) demons a e he
impo ance o selec ing he igh lesion pa ches ( hose wi h high e o alues) agains selec ing
any umo pa ch wi hou any c i e ia. I can be seen how he pe o mance o he ne wo ks
Expe imen s and Resul s 24
Figu e 4.29: Pa ch dis ibu ion e olu ion o he BaseASS model
Figu e 4.30: Pe cen age o class oxels pe ba ch pe epoch o BaseASS
imp o es om epoch 1 (Fig. 4.31(b)) o epoch 30 (Fig. 4.31(d)). We can see ha om he 15 h
o he 30 h epoch, he ne wo k wo ks o e ine he segmen a ion. Mainly, he e o lies in he
bounda ies be ween wo di e en classes.
Table 4.12, Table 4.13 and Table 4.14 show he con usion ma ices o he BaseASS wi h he wo
di e en loss unc ions and di e en a chi ec u e.
Expe imen s and Resul s 25
(a) G ound T u h
abo e MRI T1
(b) E o map in
epoch 1
(c) E o map in
epoch 15
(d) E o map in
epoch 30
(e)
Colo
scale
Figu e 4.31: E o maps om subjec B a s17 −CBICA −AAL wi h BaseASS. Ligh blue
is equi alen o ze o e o , yellow means maximum e o alue.
G P % 0 1 2 3
0 0,99914 0,00013 0,00066 0,00007
10,09024 0,61238 0,22317 0,07421
20,15804 0,06343 0,76245 0,01608
30,05271 0,04601 0,06876 0,83252
Table 4.12: Con usion ma ix BaseASS wi h c oss-en opy loss ( alida ion)
G P % 0 1 2 3
0 0,99825 0,00020 0,00140 0,00015
10,11032 0,62370 0,18580 0,08018
20,13554 0,062621 0,78282 0,01903
30,05122 0,04287 0,06184 0,84407
Table 4.13: Con usion ma ix BaseASS wi h Gene alised DSC loss ( alida ion)
G P % 0 1 2 3
0 0,99361 0,00074 0,00469 0,00096
10,12832 0,52653 0,29216 0,05300
20,11627 0,09170 0,76764 0,02439
30,04074 0,13621 0,07489 0,74816
Table 4.14: Con usion ma ix o BaseASS and Deep Medic ne wo k ( alida ion)
4.4 Discussion
In his wo k, we ha e analyzed and e alua ed 13 sampling schemes. An o e all compa ison is
done in Table 4.15. Fi s , we concluded ha o whole subjec (dense- aining) DSC pe o med
be e han c oss-en opy since he second ea s all aining oxels equally and his is no help ul
when he ne wo k has di icul ies in lea ning ep esen a ions o he mino i y classes. DSC does
an implici e-weigh ing o he oxels alle ia ing his issue.
In he con ex o pa ch sampling, ixed- ule sampling schemes ha e appea ed o be isky models
as hey o e -modi iy he aining dis ibu ion om he o iginal one, in such manne ha hey
change he model beha io making i di icul o adjus o he alida ion dis ibu ion (uni o m).
Budge 26
The bes esul was o o eg ound-backg ound sampling wi hou weigh ed loss unc ion, he
scheme among he ou which less modi ies he dis ibu ion. This esul s ha e been checked o
c oss-en opy, bu we canno ensu e wha would happen using o he loss unc ions.
Rega ding adap i e sampling, bo h CASED [25] and BaseASS [26] achie e e y good esul s.
I ’s isky o claim which one is be e han he o he because, al hough he BaseASS p esen s
he highe dice sco e and e en a li le mo e be e esul s on he con usion ma ix, he beha io
is e y simila and we do no know i we could achie e be e esul s adjus ing he models wi h
new modi ica ions. The key o he success o bo h is ha he inal dis ibu ion a he aining
end is e y close o he eal one. Hence, his gi es hem s eng h o alle ia e class imbalance
and gene alize co ec ly.
Scheme Dice Whole Dice Co e Dice Enhance
Dense- aining + C oss-en oy 0,67032 0,41302 0,50329
Dense- aining + DSC 0,80534 0,70092 0,65296
Fo eg ound-backg ound sampling scheme 0,80156 0,59277 0,59949
Pe -Class sampling scheme 0,74112 0,53220 0,567712
Fo eg ound-backg ound sampling scheme
+ WL
0,72799 0,49146 0,58795
Pe -Class sampling scheme+ WL 0,30150 0,19794 0,47847
CASED 0,84130 0,73418 0,65403
BaseASS 0,86286 0,74418 0,67466
Table 4.15: Mean Dice sco e me ics om he main expe imen s ca ied on
Boxplo s 4.32,4.33 and 4.34 show qua ile anges o he DSC sco es (Whole Tumo , Co e Tumo
and Enhancing Tumo espec i ely) on he es da ase s, do s indica e ou lie s and he ed
line indica es he median alue. They gi e us an o e iew o he beha iou o each o he
expe imen s. I could be a gued ha whole subjec wi h DSC has a compa able ou come o
BaseASS o CASED, howe e , i we look a qua ile 25 o he i s scheme, i is much lowe han
he qua ile 25 o he las wo.
Figu e 4.32: O e all Dice Whole Tumo Compa ison. Valida ion is done using he whole
subjec as inpu .

Budge 27
Figu e 4.33: O e all Dice Co e Tumo Compa ison. Valida ion is done using he whole
subjec as inpu .
Figu e 4.34: O e all Dice Enhance Tumo Compa ison. Valida ion is done using he whole
subjec as inpu .
Chap e 5
Budge
This p ojec has been ca ied in he Image P ocessing G oup, ETSETB, UPC. Deep Lea ning is
highly compu a ionally demanding, consequen ly a GPU was needed: The GPU GeFo ce GTX
Ti an Black has an app oxima e cos o 920 e, howe e UPC p o ided i o us wi hou any cos .
Thus, he main cos o his p ojec comes om he sala y o he esea che s and he ime spen
in i . The eam o he de elopmen o his hesis is o med by wo p o esso s who we e ad ising
me as senio enginee s and mysel as junio enginee . The o al du a ion o he p ojec was o
33 weeks. The budge o he p ojec can be calcula ed:
Amoun
Wage/hou
Dedica-
ion
To al
Junio
Enginee
1 8,00e/h 25h/week 6,600 e
Senio
Enginee
2 20,00e/h 4h/week 5,280 e
Table 5.1: P ojec Budge
28
Chap e 6
Conclusions and u u e
de elopmen
The main goal o his p ojec was o apply di e en s a e-o - he a me hodologies o b ain
umo segmen a ion o make a compa a i e s udy o all hem. We s udied how dense- aining
and pa ch sampling pe o med in he b ain umo segmen a ion. Fo his eason, we p oposed
a ian s o ixed- ule and adap i e sampling schemes.
In sec ion 4.2 we p o ed ha he DSC ou pe o ms c oss-en opy abili y o classi y umo /non-
umo oxels in dense- aining. Howe e , in pa ch sampling, c oss-en opy demons a ed o be
be e han weigh ed loss unc ions as weigh ed c oss-en opy and gene alised DSC.
Then, in sec ion 4.3, we show ha p ope ly designed pa ch sampling ou pe o ms dense- aining
schemes. Mo eo e , we conclude ha i we al e signi ican ly he aining dis ibu ion om
he eal, such ha using pe -class sampling scheme, we inc ease gene aliza ion e o e en i
aining imp o es due o he misma ch be ween aining and es ing dis ibu ions. Mo eo e ,
no el adap i e aining schemes a e shown o u he imp o e he pe o mance compa ed o
he ixed- ule schemes o he b ain umo segmen a ion ask. We obse ed how only adap i e
sampling ob aines good esul s al e ing he aining dis ibu ion in such a way ha achie es
lea ning he ea u es o hose segmen s ha a e mo e di icul o classi y. Ou bes esul s a e:
dice sco e o whole umo o 0,862 , dice sco e o co e umo o 0,744 and a dice sco e o
enhancing umo o 0,67.
We compa e ou esul s wi h he leade s o he MICCAI challenge anking and he esul s
p esen ed by he UPC his las edi ion (Table 6.1). Fo dice sco e o whole umo , ou me hod
is e y close o he esul s ob ained by he op pe o ming me hods while, ou me hod achie es
low dice sco e o enhancing umo and co e umo . BaseASS has simila pe o mance o he
app oach p esen ed by he UPC, in which hey ackle he p oblem wi h a pipeline o wo masked
V-Ne s and dense- aining. Howe e , ou esul s a e s ill well below he ensemble model p oposed
by UCL-TIG.
29
Appendix 30
Scheme Dice Whole Dice Co e Dice Enhance
UCL-TIG 0,9 0,83 0,78
UPC 0,87 0,63 0,71
BaseASS 0,86286 0,74418 0,67466
Table 6.1: Compa ison be ween ou app oach and some o 2017 MICCAI B aTS Challenge
Finally, he choice o di e en hype -pa ame e s o he op imiza ion and egula iza ion can
hea ily a ec he pe o mance o a model. I is o en obse ed ha he choice o op imize and
i s con igu a ion, o ins ance egula i za ion o he lea ning a e, o a la ge ex en , de e mine
whe he a good o a bad segmen a ion is ob ained. The sensi i i y o all hese hype -pa ame e s
is magni ied by he ac ha e-using he same se ing does no gua an ee o beha e well among
di e en ne wo k a chi ec u es, o e en on di e en asks and da a. Hence, i is o en di icul o
d aw gene ic and con iden conclusions wi hou spending a huge amoun o ime in op imizing
he expe imen al se ings.
In he u u e, we a e in e es ed in ying aining wi h a di e en a chi ec u es as we belie ha
his one migh be a bo leneck. We a e in e es ed in ying dila ed con olu ions as hey a e
able o in oduce sys ema ically mul i-scale con ex ual in o ma ion wi hou loosing esolu ion.
HighResNe [16] is a ne wo k which uses dila ed con olu ion and esidual connec ions. The
a chi ec u e is based on he ac ha dila ed con olu ions suppo exponen ial expansion o he
ecep i e ield wi hou loss o esolu ion and a oid max-pooling.
Now ha we al eady know ha BaseASS p o ides sucess ul esul s i would be in e es ing o do
mo e ese ach on i . The BaseASS and also he CASED s ill ha e o he lea ning pa ame e s ha
could be explo ed, o ins ance gi e p io i y o pa ches o he modali y wi h he g ea es impac .
I would also be ele an o conside a ion make adap i e o he pa ame e s as he lea ning a e
o he pa ch-size. I also has been le ying o do an ensemble o he bes me hods in his hesis.
Finally, adapa i e sampling schemes om his wo k migh be powe ul in o he segmen a ion
asks whe e imbalance is also a p oblem, like whi e ma e hype in ensi ies (WMH) segmen a ion.
Bibliog aphy
[1] E.C. Holland. P ogeni o cells and glioma o ma ion.
[2] Bjoe n Menze, And as Jakab, S e an Baue , Jayash ee Kalpa hy-C ame , Key an Fa a-
hani, Jus in Ki by, Yuliya Bu en, Nicole Po z, Johannes Slo boom, Roland Wies , Le en e
Lanczi, Elisabe h Ge s ne , Ma c-And e Webe , Tal A bel, B ian A an s, Nicholas Ay-
ache, Pa icia Buendia, Louis Collins, Nicolas Co die , Jason Co so, An onio C iminisi,
Tilak Das, He ´e Delinge e, Caga ay Demi alp, Ch is ophe Du s , Michel Doja , Senan
Doyle, Joana Fes a, Flo ence Fo bes, Ezequiel Ge emia, Ben Glocke , Polina Golland, Xi-
ao ao Guo, Andac Hamamci, Khan I ekha uddin, Raj Jena, Nigel John, Ende Konukoglu,
Danial Lashka i, Jose An onio Ma iz, Raphael Meie , Se gio Pe ei a, Doina P ecup, S. J.
P ice, Tammy Riklin-Ra i , Syed Reza, Michael Ryan, Law ence Schwa z, Hoo-Chang
Shin, Jamie Sho on, Ca los Sil a, Nuno Sousa, Nagesh Subbanna, Gabo Szekely, Thomas
Taylo , Owen Thomas, Nicholas Tus ison, Gozde Unal, Flo Vasseu , Max Win e ma k,
Dong Hye Ye, Liang Zhao, Binsheng Zhao, Da ko Zikic, Ma cel P as awa, Mau icio Reyes,
and Koen Van Leempu . The Mul imodal B ain Tumo Image Segmen a ion Benchma k
(BRATS). IEEE T ansac ions on Medical Imaging, 34(10):1993–2024, Oc obe 2014. doi:
10.1109/TMI.2014.2377694. URL h ps://hal.in ia. /hal-00935640.
[3] Mul imodal b ain umo segmen a ion challenge 2017. URL h p://www.med.upenn.edu/
sbia/b a s2017/da a.h ml.
[4] B. H. Menze, A. Jakab, S. Baue , J. Kalpa hy-C ame , K. Fa ahani, J. Ki by, Y. Bu en,
N. Po z, J. Slo boom, R. Wies , L. Lanczi, E. Ge s ne , M. A. Webe , T. A bel, B. B.
A an s, N. Ayache, P. Buendia, D. L. Collins, N. Co die , J. J. Co so, A. C iminisi, T. Das,
H. Delinge e, . Demi alp, C. R. Du s , M. Doja , S. Doyle, J. Fes a, F. Fo bes, E. Ge emia,
B. Glocke , P. Golland, X. Guo, A. Hamamci, K. M. I ekha uddin, R. Jena, N. M. John,
E. Konukoglu, D. Lashka i, J. A. Ma iz, R. Meie , S. Pe ei a, D. P ecup, S. J. P ice, T. R.
Ra i , S. M. S. Reza, M. Ryan, D. Sa ikaya, L. Schwa z, H. C. Shin, J. Sho on, C. A. Sil a,
N. Sousa, N. K. Subbanna, G. Szekely, T. J. Taylo , O. M. Thomas, N. J. Tus ison, G. Unal,
F. Vasseu , M. Win e ma k, D. H. Ye, L. Zhao, B. Zhao, D. Zikic, M. P as awa, M. Reyes,
and K. Van Leempu . The mul imodal b ain umo image segmen a ion benchma k (b a s).
IEEE T ansac ions on Medical Imaging, 34(10):1993–2024, Oc 2015. ISSN 0278-0062. doi:
10.1109/TMI.2014.2377694.
[5] Fei-Fei Li, Jus in Johnson, and Se ena Yeung. Cs231n: Con olu ional neu al ne wo ks o
isual ecogni ion., 2017. URL h p://cs231n.s an o d.edu/.
37

Bibliog aphy 38
[6] Mohammad Ha aei, Axel Da y, Da id Wa de-Fa ley, An oine Bia d, Aa on C. Cou ille,
Yoshua Bengio, Ch is Pal, Pie e-Ma c Jodoin, and Hugo La ochelle. B ain umo segmen-
a ion wi h deep neu al ne wo ks. CoRR, abs/1505.03540, 2015. URL h p://a xi .o g/
abs/1505.03540.
[7] e al Ad i`a Casami jana. 3D Con olu ional Neu al Ne wo ks o B ain Tumo Segmen a ion:
a compa ison o mul i- esolu ion a chi ec u es. In e na ional Wo kshop on B ainlesion:
Glioma, Mul iple Scle osis, S oke and T auma ic B ain Inju ies. Sp inge , Cham, 2016.
[8] F an¸cois Cholle e al. Ke as. h ps://ke as.io, 2015.
[9] Ian Good ellow, Yoshua Bengio, and Aa on Cou ille. Deep Lea ning. MIT P ess, 2016.
h p://www.deeplea ningbook.o g.
[10] S´e gio Pe ei a, Ad iano Pin o, Vic o Al es, and Ca los A. Sil a. Deep con olu ional neu al
ne wo ks o he segmen a ion o gliomas in mul i-sequence m i. In Alessand o C imi,
Bjoe n Menze, Oska Maie , Mau icio Reyes, and Heinz Handels, edi o s, B ainlesion:
Glioma, Mul iple Scle osis, S oke and T auma ic B ain Inju ies, pages 131–143, Cham,
2016. Sp inge In e na ional Publishing. ISBN 978-3-319-30858-6.
[11] Kons an inos Kamni sas, Ch is ian Ledig, Vi ginia F. J. Newcombe, Joanna P. Simpson,
And ew D. Kane, Da id K. Menon, Daniel Ruecke , and Ben Glocke . E icien mul i-
scale 3d CNN wi h ully connec ed CRF o accu a e b ain lesion segmen a ion. CoRR,
abs/1603.05959, 2016. URL h p://a xi .o g/abs/1603.05959.
[12] Ma cel Ca `a, Ad i`a Casami jana, I ina S´anchez, Ma c Combalia, and Ve ´onica Vilaplana.
Masked -ne : an app oach o b ain umo segmen a ion.
[13] ¨
Ozg¨un C¸i¸cek, Ahmed Abdulkadi , Soe en S. Lienkamp, Thomas B ox, and Ola Ron-
nebe ge . 3d u-ne : Lea ning dense olume ic segmen a ion om spa se anno a ion. CoRR,
abs/1606.06650, 2016. URL h p://a xi .o g/abs/1606.06650.
[14] Ola Ronnebe ge , Philipp Fische , and Thomas B ox. U-ne : Con olu ional ne wo ks o
biomedical image segmen a ion. CoRR, abs/1505.04597, 2015. URL h p://a xi .o g/
abs/1505.04597.
[15] Rupesh Kuma S i as a a, Klaus G e , and J¨u gen Schmidhube . Highway ne wo ks.
CoRR, abs/1505.00387, 2015. URL h p://a xi .o g/abs/1505.00387.
[16] Wenqi Li, Guo ai Wang, Lucas Fidon, S´ebas ien Ou selin, M. Jo ge Ca doso, and Tom
Ve cau e en. On he compac ness, e iciency, and ep esen a ion o 3d con olu ional
ne wo ks: B ain pa cella ion as a p e ex ask. CoRR, abs/1707.01992, 2017. URL
h p://a xi .o g/abs/1707.01992.
[17] P ep oceedings 2017 In e na ional MICCAI B aTS Challenge, 2017. MICCAI,CBICA.
URL h ps://www.cbica.upenn.edu/sbia/Spy idon.Bakas/MICCAI_B aTS/MICCAI_
B aTS_2017_p oceedings_sho Pape s.pd .
[18] Kons an inos Kamni sas, Wenjia Bai, Enzo Fe an e, S e en G. McDonagh, Ma hew Sin-
clai , Nick Pawlowski, Ma in Rajchl, Ma hew C. H. Lee, Be nha d Kainz, Daniel Ruecke ,
Bibliog aphy 39
and Ben Glocke . Ensembles o mul iple models and a chi ec u es o obus b ain umou
segmen a ion. CoRR, abs/1711.01468, 2017. URL h p://a xi .o g/abs/1711.01468.
[19] Tom B osch, Youngjin Yoo, Lisa Y. W. Tang, Da id K. B. Li, An hony T aboulsee, and
Roge Tam. Deep con olu ional encode ne wo ks o mul iple scle osis lesion segmen a ion.
In Nassi Na ab, Joachim Ho negge , William M. Wells, and Alejand o F. F angi, edi o s,
Medical Image Compu ing and Compu e -Assis ed In e en ion – MICCAI 2015, pages 3–
11, Cham, 2015. Sp inge In e na ional Publishing. ISBN 978-3-319-24574-4.
[20] Faus o Mille a i, Nassi Na ab, and Seyed-Ahmad Ahmadi. V-ne : Fully con olu ional
neu al ne wo ks o olume ic medical image segmen a ion. CoRR, abs/1606.04797, 2016.
URL h p://a xi .o g/abs/1606.04797.
[21] Ca ole H. Sud e, Wenqi Li, Tom Ve cau e en, S´ebas ien Ou selin, and M. Jo ge Ca doso.
Gene alised dice o e lap as a deep lea ning loss unc ion o highly unbalanced segmen a-
ions. CoRR, abs/1707.03237, 2017. URL h p://a xi .o g/abs/1707.03237.
[22] Mul imodal B ain Tumo Image Segmen a ion Benchma k: Change De ec ion, 2016. MIC-
CAI,CBICA.
[23] Cs229: Addi ional no es on backp opaga ion, 2017. URL h p://cs229.s an o d.edu/
no es/cs229-no es-backp op.pd .
[24] Lucas Fidon, Wenqi Li, Luis C. Ga c´ıa-Pe aza-He e a, Jinend a Ekanayake, Neil Ki chen,
S´ebas ien Ou selin, and Tom Ve cau e en. Gene alised wasse s ein dice sco e o imbalanced
mul i-class segmen a ion using holis ic con olu ional ne wo ks. CoRR, abs/1707.00478,
2017. URL h p://a xi .o g/abs/1707.00478.
[25] Jesson A., Guiza d N., Ghalehjegh S.H., Goblo D., Soudan F., and Chapados N. Cased:
Cu iculum adap i e sampling o ex eme da a imbalance. 10435, 2017.
[26] Lo enz Be ge , Eoin Hyde, M. Jo ge Ca doso, and S´ebas ien Ou selin. An adap i e sampling
scheme o e icien ly ain ully con olu ional ne wo ks o seman ic segmen a ion. CoRR,
abs/1709.02764, 2017. URL h p://a xi .o g/abs/1709.02764.
[27] Kaiming He, Xiangyu Zhang, Shaoqing Ren, and Jian Sun. Del ing deep in o ec i ie s:
Su passing human-le el pe o mance on imagene classi ica ion. CoRR, abs/1502.01852,
2015. URL h p://a xi .o g/abs/1502.01852.
[28] Diede ik P. Kingma and Jimmy Ba. Adam: A me hod o s ochas ic op imiza ion. CoRR,
abs/1412.6980, 2014. URL h p://a xi .o g/abs/1412.6980.
[29] Thesis. URL h ps://gi hub.com/cla abonnin/segmen a ion_DLMI_cla a.