FYI
------------------------
-------- Original Message --------
Subject: PhD scholarships, Heidelberg University
Date: Tue, 5 Jul 2011 22:37:26 +0200
From: Sebastian Padó <pado(a)cl.uni-heidelberg.de>
Reply-To: Sebastian Padó <pado(a)cl.uni-heidelberg.de>
To: researchers(a)pascal-network.org
5 PhD scholarships in Computational Linguistics: "Semantics beyond the
sentence" (Date: July 5th 2011, Deadline: July 31st)
We are soliciting applications for 5 PhD scholarships (EUR 1310 per
month, tax-free) within the research initiative "Coherence in Language
Processing: Semantics Beyond the Sentence". They are associated with
the Graduate Program "Semantic Processing", jointly organized by the
Computational Linguistics Department (ICL) at Heidelberg University
[1] and the NLP Group at HITS gGmbH [2] in Heidelberg, Germany. The
scholarships are available from October 1st, 2011, and will run three
years (dependent on positive evaluations after the first and second
years).
The goal of the research initiative "Coherence in Language Processing:
Semantics Beyond the Sentence" is to investigate computational models
of semantic phenomena at the discourse level by (a) analysing semantic
phenomena at the discourse level and represent them; (b) using these
representatons to improve semantic analysis; (c) evaluating (a) and
(b) in NLP applications, including SMT. See [3] for details.
Candidates should have a strong background in computational
linguistics and possess a Masters or a Diploma degree in either
Computational Linguistics or Computer Science/Linguistics with a
specialization in Natural Language Processing. Experience with machine
learning, corpus-based methods and statistics is a plus. Strong
programming skills (Java, C++, or Python) are required.
Scholarship holders will become members of the graduate program
"Semantic Processing" [4]. They will participate in a PhD colloquium
and may attend lectures at the university and the Heidelberg Graduate
School "MathComp" [5]. The graduate program provides a lively research
environment with about ten PhD students already
enrolled. Interdisciplinary research links exist to computer science,
linguistics, and other disciplines.
Applications should include a research statement indicating the
candidates' interests and plans (which should fall into the area
outlined above), university transcripts and a CV. They should also
indicate a preference for a primary supervisor matching their plans
(Anette Frank, Sebastian Pado, Stefan Riezler, Michael Strube). For
more details, see the links below.
Please send your application, including all documents, as a single PDF
file before **July 31st 2011** to:
Anke Sopka & Corinna Schwarz
Sekretariat Computerlinguistik
sekretariat(a)cl.uni-heidelberg.de
Questions should be sent to Sebastian Pado, pado(a)cl.uni-heidelberg.de
Links:
[1] ICL (http://www.cl.uni-heidelberg.de)
[2] HITS (http://www.h-its.org/nlp)
[3] Research Initiative Discourse Semantics
http://semproc.cl.uni-heidelberg.de/discourse-semantics/
[4] Graduate Program Semantic Processing
http://semproc.cl.uni-heidelberg.de
[5] Heidelberg Graduate School in Mathematical
and Computational Methods for the Sciences
http://www.mathcomp.uni-heidelberg.de/
--
Sebastian Pado pado(a)cl.uni-heidelberg.de
Institut für Computerlinguistik www.cl.uni-heidelberg.de/~pado
Universität Heidelberg Tel. 06221 - 54 3591
Im Neuenheimer Feld 325, 69120 HD Fax 06221 - 54 3242
--
Gary Green
FYI
-------forwarded message----------
Programme Leader/Programme Leader Track
Cambridge
The MRC Cognition and Brain Sciences Unit (CBSU) is an internationally
renowned research institute with state-of-the-art cognitive neuroscience
facilities, including a research dedicated 3T Siemens TIM Trio MRI
scanner and 306-channel Elekta Neuromag MEG scanner.
We are seeking a talented new Group Leader to lead and manage the
Methods group at the Unit. The role of the group is both to provide
support for analysis of behavioural, fMRI, M/EEG data, DTI and other
data, and to develop and apply innovative methods to support the CBSU
mission to deliver world-class research on human cognition and its
biological underpinnings.
The post will be ideal for a senior postdoctoral scientist with an
outstanding record of scientific achievement, wishing to establish an
independent career in the field of cognitive neuroscience. You will
have a strong background in a relevant discipline (e.g., training in
signal processing, mathematics, physics, statistics, or computer
science), and experience of the type of methods and questions addressed
within human cognitive neuroscience.
This appointment may be made at either Programme Leader (starting salary
£44,314) or Programme Leader Track (starting salary £35,935) level.
This is supported by a flexible pay and reward policy, and optional MRC
final salary Pension Scheme. We offer 30 days annual leave entitlement.
Applications are handled by the RCUK Shared Services Centre; to apply
please visit our job board at https://ext.ssc.rcuk.ac.uk and complete an
online application form. Applicants who would like to receive this
advert in an alternative format (e.g. large print, Braille, audio or
hard copy), or who are unable to apply online should contact us by
telephone on 01793 867003, Please quote reference number IRC24431.
Closing date: 31st August 2011
--
Dear Users
This Thursday (4-5 pm) there will be a project proposal presentation given
by Rich Harris. The title of Rich's talk is "The neural representation of
perceived changes in facial expression". Please see below for the talk
abstract.
Everyone is welcome to attend and refreshments will be provided.
Best wishes
Rebecca
Abstract:
How the brain represents different aspects of faces remains controversial.
This experiment will present participants with stimuli drawn from morphed
continua between two different emotional facial expressions. In paired
presentations, a second face could: (1) be identical to the first; (2) share
the perceived expression category but differ physically along the morphed
continuum (within-expression change); (3) differ physically by the same
distance along the continuum but in a direction that leads participants to
classify the face pairs as showing expressions of different basic emotions
(between-expression change). Using an fMR-adaptation paradigm, our aim is to
reveal regions of the brain whose activity corresponds to our sensitivity to
changes in facial expression.
--
Dr. Rebecca E. Millman
York Neuroimaging Centre
The Biocentre
York Science Park
York
YO10 5DG
Email: rem(a)ynic.york.ac.uk
Tel: 01904 435 5373
Hi,
We've added Matlab 7.12 (R2011a) to the YNiC systems. The default has
not yet changed and remains 7.10 (R2010a). Details of the supported
versions are at:
https://www.ynic.york.ac.uk/doc/ITPages/FAQ/Misc/SupportedVersions#Matlab
At the same time, we've updated SPM8 to the latest revision which is
8+svn4290.
Can people please test the new Matlab version as we'll change the
default in September unless any major issues are found. We'll also be
looking to withdraw Matlab 7.8 in September (as previously announced) as
part of a major set of software upgrades. More on this later.
Thanks,
Mark
--
Mark Hymers
York Neuroimaging Centre
Dear Users
Today (4-5 pm in YNiC) there will be a project proposal presentation by
Carin Whitney. The title of the project is "Investigating semantic
cognition with MEG, fMRI and TMS". Please see below for the talk abstract.
Everyone is welcome to attend and refreshments will be provided after
the talk.
Best wishes
Rebecca
Abstract:
Beth Jefferies, Carin Whitney, Piers Cornelissen and Andy Ellis
This project investigates how semantic cognition – referring to our
ability to understand the meaning of words, pictures, faces, sounds, and
smells – is represented in the brain. We will focus on semantic control,
which is one of two principal components of semantic cognition and
relates to executive mechanisms that enable us to retrieve and select
conceptual knowledge according to the current task or context.
Research has been plentiful in describing the spatial extent of the
brain regions that underpin semantic control, and has identified a
distributed fronto-temporo-parietal network. However, it remains largely
unknown how this system is organised (i.e., what the specific functions
of each component are) and how well they interact. In the proposed
project, we will apply a novel approach to investigate these questions
by combining MEG with TMS and fMRI. In particular, we will use MEG to
track neural activity, allowing us to generate predictions about likely
patterns of communication within the semantic control network and its
relation to other components of semantic cognition (i.e., brain areas
that encode conceptual knowledge). Follow-up TMS will then be used to
impair brain functioning at specific time points to prove causality.
Equivalent fMRI data – taken from the same participants and tasks – will
guide coil positioning for TMS and act as a spatial localiser for MEG.
The project hence aims to establish a neural model of semantic cognition
that is based on convergent evidence across different methods,
generating potentially strong conclusions about how meaning retrieval is
achieved.
--
************************************************************************
Dr. Rebecca E. Millman
Science Liaison Officer
York Neuroimaging Centre
The Biocentre
York Science Park
Heslington
YO10 5DG
Tel: +44 (0) 1904 567614
Fax: +44 (0) 1904 435356
Dear Users
This Thursday (4-5 pm in YNiC) there will be a project proposal
presentation by Carin Whitney. The title of the project is
"Investigating semantic cognition with MEG, fMRI and TMS". Please see
below for the talk abstract.
Everyone is welcome to attend and refreshments will be provided after
the talk.
Best wishes
Rebecca
Abstract:
Beth Jefferies, Carin Whitney, Piers Cornelissen and Andy Ellis
This project investigates how semantic cognition – referring to our
ability to understand the meaning of words, pictures, faces, sounds, and
smells – is represented in the brain. We will focus on semantic control,
which is one of two principal components of semantic cognition and
relates to executive mechanisms that enable us to retrieve and select
conceptual knowledge according to the current task or context.
Research has been plentiful in describing the spatial extent of the
brain regions that underpin semantic control, and has identified a
distributed fronto-temporo-parietal network. However, it remains largely
unknown how this system is organised (i.e., what the specific functions
of each component are) and how well they interact. In the proposed
project, we will apply a novel approach to investigate these questions
by combining MEG with TMS and fMRI. In particular, we will use MEG to
track neural activity, allowing us to generate predictions about likely
patterns of communication within the semantic control network and its
relation to other components of semantic cognition (i.e., brain areas
that encode conceptual knowledge). Follow-up TMS will then be used to
impair brain functioning at specific time points to prove causality.
Equivalent fMRI data – taken from the same participants and tasks – will
guide coil positioning for TMS and act as a spatial localiser for MEG.
The project hence aims to establish a neural model of semantic cognition
that is based on convergent evidence across different methods,
generating potentially strong conclusions about how meaning retrieval is
achieved.
--
************************************************************************
Dr. Rebecca E. Millman
Science Liaison Officer
York Neuroimaging Centre
The Biocentre
York Science Park
Heslington
YO10 5DG
Tel: +44 (0) 1904 567614
Fax: +44 (0) 1904 435356
Dear Users
Today (4-5 pm in YNiC) there will be a talk by Prof. Peter Redgrave from
the University of Sheffield.
http://www.sheffield.ac.uk/psychology/staff/academic/peter-redgrave
The title of Prof. Redgrave's talk is "Goal-directed and habitual
control in the basal ganglia: implications
for Parkinson's disease". Please see below for the talk abstract.
Everyone is welcome to attend and refreshments will be provided after
the talk.
Best wishes
Rebecca
Abstract:
Progressive loss of the ascending dopaminergic projection in the basal
ganglia is a fundamental pathological feature of Parkinson’s disease.
Studies in animals and humans have identified spatially segregated
functional territories in the basal ganglia for the control of
goal-directed and habitual actions. In patients with Parkinson’s disease
the loss of dopamine is predominantly in the posterior putamen, a region
of the basal ganglia associated with the control of habitual behaviour.
These patients may therefore be forced into a progressive reliance on
the goal-directed mode of action control that is mediated by
comparatively preserved processing in rostro-medial striatum. Thus, in
addition of the loss of habits, the behavioural difficulties of
Parkinson patients may also be subject to distorting output signals from
habitual control circuits which impede the expression of goal-directed
action.
--
************************************************************************
Dr. Rebecca E. Millman
Science Liaison Officer
York Neuroimaging Centre
The Biocentre
York Science Park
Heslington
YO10 5DG
Tel: +44 (0) 1904 567614
Fax: +44 (0) 1904 435356
Dear Users
This Thursday (4-5 pm in YNiC) there will be a talk by Prof. Peter
Redgrave from the University of Sheffield.
http://www.sheffield.ac.uk/psychology/staff/academic/peter-redgrave
The title of Prof. Redgrave's talk is "Goal-directed and habitual
control in the basal ganglia: implications
for Parkinson's disease". Please see below for the talk abstract.
Everyone is welcome to attend and refreshments will be provided after
the talk.
Best wishes
Rebecca
Abstract:
Progressive loss of the ascending dopaminergic projection in the basal
ganglia is a fundamental pathological feature of Parkinson’s disease.
Studies in animals and humans have identified spatially segregated
functional territories in the basal ganglia for the control of
goal-directed and habitual actions. In patients with Parkinson’s disease
the loss of dopamine is predominantly in the posterior putamen, a region
of the basal ganglia associated with the control of habitual behaviour.
These patients may therefore be forced into a progressive reliance on
the goal-directed mode of action control that is mediated by
comparatively preserved processing in rostro-medial striatum. Thus, in
addition of the loss of habits, the behavioural difficulties of
Parkinson patients may also be subject to distorting output signals from
habitual control circuits which impede the expression of goal-directed
action
--
************************************************************************
Dr. Rebecca E. Millman
Science Liaison Officer
York Neuroimaging Centre
The Biocentre
York Science Park
Heslington
YO10 5DG
Tel: +44 (0) 1904 567614
Fax: +44 (0) 1904 435356
Hi,
We have just pushed some core changes to the YNiC NAF Beamforming code.
The change is that nafEpochRejection will no longer produce what have
become known as "Epoch Rejection Files" but will instead produce "Slice
Rejection Files".
"Epoch Rejection File" are simply a list of epochs of data which should
be rejected during analysis due to artifacts. This can be problematic,
as if you change your pre-trigger or epoch duration, the timings of the
epochs will move around and you will reject data you didn't mean to,
whilst not rejecting the data around your artifacts.
The replacement for these are "Slice Rejection Files". These are a list
of slice ranges containing bad data - simply a list of comma separated
slice ranges; one per line.
The analysis (beamformer) code itself will continue to accept Epoch
Rejection Files which are listed in YAML files for analysis, but will
produce "Deprecation Warnings" to remind you that you should consider
converting.
If you wish to convert an existing Epoch Rejection File to a Slice
Rejection File, you can do one of the following:
* Use the nafEpochRejectToSliceReject tool (documented at
/mnt/common/naf/naf-doc/userref/scripts/nafEpochRejectToSliceReject.html )
* Load the Epoch Rejection file into nafEpochRejection using the -e
flag and it will output a slice rejection file.
* Load you study into the Study Definer Tool (nafStudyDefiner) and it
will offer to convert all epoch rejection files into slice rejection
files and update the YAML file for you at the same time.
Although the nafEpochRejection and nafStudyDefiner tool will still read
Epoch Rejection Files (to perform conversions), they will no longer
allow you to edit or output them; they will only work with and output
slice rejection files.
It should be noted that internally, all of the code now converts Epoch
Rejection Files to Slice Rejection Files. This means that strictly
speaking, if you have overlapping epochs, a single epoch number in an
epoch rejection may now result in more than one epoch being rejected.
This should be a rare corner case and if you want to fully understand
and see what is going on, you can use the nafShowEpochs tool to list the
epochs you have and, if a epoch or slice rejection file is present in your
YAML file, whether or not they will be rejected.
This is one of the final big changes before we make the NAF tools
available by default on the system. More on that soon.
Thanks,
Mark
--
Mark Hymers
York Neuroimaging Centre
Dear all,
We need to reboot the main fileservers at YNiC over the weekend, most
likely on Saturday. Can I therefore ask that people log off at the end
of Friday and do not leave jobs running on the cluster which will
continue beyond Saturday morning - any jobs running at that point will
be cancelled.
This does not affect the Psychology email server.
Thanks,
Mark
--
Mark Hymers
York Neuroimaging Centre
FYI
-------------------------------
Dear colleagues,
please find below two separate announcements for open positions
in our research team.
Kind regards,
Alfons Schnitzler & Katja Biermann-Ruben
/**********************************************************************/
PhD Position in Düsseldorf
A *PhD position* is available at the Institute of Clinical Neuroscience
and Medical Psychology, Heinrich-Heine-University Düsseldorf, to study
neural representations of action related concepts.
The successful candidate will be expected to work within the
interdisciplinary collaborative research center (CRC/SFB 991) "The
Structures of Representation in Language, Science and Cognition"
starting July 2011. Within this linguistic CRC and on the theoretical
basis of embodiment and the mirror neuron system our neuroscientific
project investigates the functional relevance of the motor cortex for
conceptual representation of verbs and nouns which derived from action
verbs. Methods will be non-invasive 306-channel MEG, TMS and behavioural
priming.
Successful candidates will have a MSc in psychology, neuroscience or
related fields and are highly motivated to learn MEG and TMS measurement
and data analysis. Preference will be given to candidates with
experimental practice.
We offer a stimulating and inspiring atmosphere in a young,
interdisciplinary team of neurologists, psychologists, physicists, and
biologists.
The position is for an initial period of two years but may be extended.
Earliest start for the position is July 2011. Applications will be
accepted until the position is filled.
To apply, please send a full CV, a brief outline of current research and
interests, certificates, and contact information of two academic
references via email to/: schnitza(a)med.uni-duesseldorf.de and
K.Biermann-Ruben(a)uni-duesseldorf.de/
/ /
Or via regular mail to: Dr. Katja Biermann-Ruben,
Heinrich-Heine-University Düsseldorf, Institute of Clinical Neuroscience
and Medical Psychology, Moorenstr. 5, D-40225 Düsseldorf
//
/**********************************************************************/
//
//
PostDoc Position in Düsseldorf
A *postdoctoral position* is available at the Institute of Clinical
Neuroscience and Medical Psychology, Heinrich-Heine-University
Düsseldorf, to study neural representations of action related concepts.
The successful candidate will be expected to play a key role in our
neuroscientific the interdisciplinary collaborative research center
(CRC/SFB 991) "The Structures of Representation in Language, Science and
Cognition" starting July 2011. Within this linguistic CRC and on the
theoretical basis of embodiment and the mirror neuron system our project
investigates the functional relevance of the motor cortex for conceptual
representation of verbs and nouns which derived from action verbs.
Methods will be non-invasive 306-channel MEG, TMS and behavioural priming.
Successful candidates will have a PhD in neuroscience or related fields.
Preference will be given to candidates with a strong background in
systems level neurophysiological research (MEG/EEG, TMS) and related
signal analysis methods (MEG/EEG analysis in frequency and time domain).
We offer a stimulating and inspiring atmosphere in a young,
interdisciplinary team of neurologists, psychologists, physicists, and
biologists.
The position is for a period of four years. Earliest is July 2011.
Applications will be accepted until the position is filled.
To apply, please send a full CV, a brief outline of current research and
interests, certificates, and contact information of two academic
references via email to/: //schnitza(a)med.uni-duesseldorf.de// and
//K.Biermann-Ruben(a)uni-duesseldorf.de/
/ /
Or via regular mail to: Dr. Katja Biermann-Ruben,
Heinrich-Heine-University Düsseldorf, Institute of Clinical Neuroscience
and Medical Psychology, Moorenstr. 5, D-40225 Düsseldorf
//
//**********************************************************************//
//
*Alfons Schnitzler, MD*
Professor and Chairman
Institute of Clinical Neuroscience and Medical Psychology
Heinrich Heine University Düsseldorf
Universitätstr. 1, D-40225 Düsseldorf
tel. ++49 211-81-13014
fax ++49 211-81-13015
&
Movement Disorders and Neuromodulation
Department of Neurology, University Hospital Düsseldorf
Moorenstr. 5, D-40225 Düsseldorf
tel. ++49 211-81-16756
fax ++49 211-81-19032
*Katja Biermann-Ruben, PhD*
Postdoctoral scientist
Institute of Clinical Neuroscience and Medical Psychology
Heinrich-Heine-University Düsseldorf
Universitätsstr. 1, D-40225 Düsseldorf
tel. ++49 211-81-13015
fax ++49 211-81-13015
FYI
-
MRC Cognition and Brain Sciences Unit – Cambridge
Research Assistant
The MRC Cognition and Brain Sciences Unit (CBSU) is an internationally
renowned research institute with state-of-the-art cognitive neuroscience
facilities, including on-site fMRI, MEG, and EEG laboratories, and
neuropsychological patient panel and large panel of healthy volunteers.
Applications are invited for a Research Assistant to provide scientific
support for Dr Tristan Bekinschtein’s 5 year programme on Transition of
Consciousness in Sleep and Sedation, particularly for acquiring
behavioural, EEG and fMRI data (and the combination of both) during
cognitive experiments on volunteers, patients with sleep disorders and
people under sedation. This is a 2 year post initially, funded by the
Wellcome Trust.
You will be highly motivated and proactive, with a degree in psychology,
biology, computer science or physics. Experience in scientific research,
particularly with human volunteers, is important, as is familiarity with
computer programming and statistics. Experience of research in the area
of sleep and polysomnography is desirable. Experience with EEG or MRI
acquisition and/or analysis would be an advantage. Good communication
skills plus the ability to work as part of a large, multi-disciplinary
team are essential.
The starting salary will be in the range of £20,074 - £27,271 per annum,
depending upon qualifications and experience. We offer a flexible pay
and reward policy, 30 days annual leave entitlement, and an optional MRC
final salary Pension Scheme. On site car and bicycle parking is available.
Applications are handled by the RCUK Shared Services Centre; to apply
please visit our job board at https://ext.ssc.rcuk.ac.uk and complete an
online application form. If you are unable to apply online please
contact us on 01793 867003 quoting reference IRC23030.
Closing date: 2nd July 2011
This position is subject to pre-employment screening
The Medical Research Council is an Equal Opportunities Employer
-------------------------
Gary Green
Dear Users
This afternoon (4-5 pm in YNiC) there will be a talk on "Measuring the
spatial resolution of MEG beamformers" given by Sam Johnson.
Everyone is welcome to attend.
Best wishes
Rebecca
--
************************************************************************
Dr. Rebecca E. Millman
Science Liaison Officer
York Neuroimaging Centre
The Biocentre
York Science Park
Heslington
YO10 5DG
Tel: +44 (0) 1904 567614
Fax: +44 (0) 1904 435356
Hi,
The UPS in the YNiC server room will be undergoing its yearly
maintanence tomorrow from around 11:30. This should have no effect on
users unless we suffer from a power cut at exactly the same time as the
UPS is being maintained (a highly unlikely scenario). In this case,
there will be a short outage whilst we bring the servers back up again.
Thanks, and sorry for the short notice.
Mark
--
Mark Hymers
York Neuroimaging Centre
FYI
***********************************
UNIVERSITY OF ABERDEEN
SCHOOL OF PSYCHOLOGY
LECTURESHIPS
As part of its continuing development, the School of Psychology invites
applications for lectureships from individuals with a strong research
record that extends the School’s activities in any of the following
areas: Cognition, Perception & Attention, and Social Cognition. The
successful candidate will show exceptional promise as an independent
researcher and the ability to deliver inspiring teaching.
Salary will be at the appropriate point on the Grade 7 scale
(£36,862-£44,016 per annum), with placement according to qualifications
and experience.
/ /
Informal enquiries may be made to Prof. Neil Macrae (tel: 01224 272245,
email c.n.macrae(a)abdn.ac.uk <mailto:c.n.macrae@abdn.ac.uk>).
* *
*Should you require a visa to undertake paid employment in the UK you
will be required to fulfil the minimum points criteria to be granted a
Certificate of Sponsorship and Tier 2 visa. As appropriate, at the time
an offer of appointment is made you will be asked to demonstrate that
you fulfil the criteria in respect of financial maintenance and
competency in English. Please do not hesitate to contact Lynda Johnston,
HR Adviser, for further information on this.*
* *
To apply online for this position visit www.abdn.ac.uk/jobs
<http://www.abdn.ac.uk/jobs>
Job Reference Number: YPS243A.
The closing date for the receipt of applications is 24 June 2011.
Promoting Diversity and Equal Opportunities throughout the University
Dr Jasna Martinovic
School of Psychology
University of Aberdeen
William Guild Building
Aberdeen
AB24 2UB
tel: 01224 272240
email: j.martinovic @ abdn.ac.uk
web: http://www.abdn.ac.uk/~psy527/dept/
--
Gary Green
York Neuroimaging Centre
The Biocentre
York Science Park
Innovation Way
Heslington
York
YO10 5DG
http://www.ynic.york.ac.ukhttps://www.ynic.york.ac.uk/about-us/people/ggrg
tel. +44 (0) 1904 435349
PA - Claire Fox : +44 (0) 1904 435329 or Claire.Fox(a)ynic.york.ac.uk
fax +44 (0) 1904 435356
mobile +44 (0) 788 191 3004
Dear Users
This Thursday (4-5 pm in YNiC) there will be a talk on "Measuring the
spatial resolution of MEG beamformers" given by Sam Johnson.
Everyone is welcome to attend.
Best wishes
Rebecca
--
Dr. Rebecca E. Millman
York Neuroimaging Centre
The Biocentre
York Science Park
York
YO10 5DG
Email: rem(a)ynic.york.ac.uk
Tel: 01904 435 5373
Hi,
FreeSurfer has recently announced a new version (5.1.0) where they've
finally sorted out the license issues after several years.
We don't have packages built for it yet, but will be looking at it very
soon (in conjunction with the neurodebian team) to replace the
semi-working 4.5.0 packages we have now.
Release notes can be found at:
http://surfer.nmr.mgh.harvard.edu/fswiki/ReleaseNotes
Thanks,
Mark
--
Mark Hymers
York Neuroimaging Centre
This evening we are hosting a visit from members of the York
Philosophical Society. They will be in YNiC from 6-8pm.
If anyone would like to help us show people around, please contact me
Gary
--
Gary Green
York Neuroimaging Centre
The Biocentre
York Science Park
Innovation Way
Heslington
York
YO10 5DG
http://www.ynic.york.ac.ukhttps://www.ynic.york.ac.uk/about-us/people/ggrg
tel. +44 (0) 1904 435349
PA +44 (0) 1904 435329 or reception(a)ynic.york.ac.uk
fax +44 (0) 1904 435356
mobile +44 (0) 788 191 3004
Dear Users
Today (4-5 pm in YNiC) there will be a YNiC project proposal
presentation given by Chris Racey.
The title of the talk is "The effects of parametrically manipulating view
exposure range on representational invariance in object selective
cortex". Please see the abstract below.
Everyone is welcome to attend.
N.B. The starting time of the YNiC seminars will be 4 pm this term.
Best wishes
Rebecca
*Abstract*
Previously we have carried out two experiments in which view shift
of objects and landscape scenes was parametrically manipulated. In both
experiments participants viewed blocks of stimuli changing in view by 0,
5, 10, and 15°. Different levels of adaptation across these view
shift conditions allow us to derive a measure of view sensitivity for any
given voxel or region. We were able to show variation in the degree of
view sensitivity between category selective regions for both objects and
landscape stimuli. Our previous work has shed new light on how category
specific visual information is processed and represented during
perception. However, it is not yet clear what the effect of object
learning and long term storage is on these ventral stream
representations. Previous research on this issue is limited, and there
have been few studies investigating the effects of prior learning on
neural adaptation.
We aim to apply our parametric manipulation of view shift paradigm
during an encoding experiment with unfamiliar objects prior to scanning.
Participants will under training, and learn to recognise objects where
their range of view exposure will vary parametrically, from 0°,
10°, and 20°. In the scanner, all of the stimuli will be
presented from previously unseen views in an fMR-adaptation block design,
with blocks of images shifting in view in 10° steps. For each
pre-exposure condition, the presentation conditions in the scanner will
be identical, and any differences across conditions must be due to
differences during the encoding of items. We predict that objects learned
with a greater range of views will be associated with richer, more
invariant, representations, and show greater degrees of invariant
adaptation than objects learned under a narrower range of views.
--
Dr. Rebecca E. Millman
York Neuroimaging Centre
The Biocentre
York Science Park
York
YO10 5DG
Email: rem(a)ynic.york.ac.uk
Tel: 01904 435 5373
FYI
---------------------
We are looking for two bright and motivated researchers to work on a
research project in which we will use *brain imaging and advanced brain
decoding methods to investigate the neural basis of deviant mental
representations in neurodevelopmental disorders such as autism,
dyslexia, and dyscalculia*. This project is an interdisciplinary
collaboration between the Laboratory of Biological Psychology (Hans Op
de Beeck), the Parenting and Special Education Research Group (Bert De
Smedt), and Child Psychiatry (Jean Steyaert, Bart Boets), all part of
the University of Leuven (K.U.Leuven) in Belgium.
We offer one PhD position and one Post-doc position. Eligible candidates
should have or should soon obtain a master’s degree (for the PhD
position) and a PhD (for the postdoc position) in a relevant field such
as neuroscience, psychology, psychiatry, neurobiology, or medical
engineering. Specific positive points for the evaluation will be
experience with brain imaging (in particular functional magnetic
resonance imaging), a computational background in a relevant field
(e.g., brain imaging data analysis, neural networks, etc.), and good
computer skills (e.g., Matlab). A background in neurodevelopmental
disorders is a plus, but not mandatory. Good English (oral and written)
communicative skills are necessary.
The two positions are full-time, for a period of 4 years (PhD position)
and 2-3 years (postdoc), and start in October 2011. The two positions
are strongly research oriented, and teaching and/or administration load
will be minimal. The research will be embedded in a very stimulating
environment with state-of-the-art technical facilities and with ample
opportunities for interaction with experts on neurodevelopmental
disorders and brain imaging. The K.U.Leuven is consistently ranked
within the top of European Universities and is located in the city of
Leuven, which has an strong international appeal. For more information
about our university, please visit http://www.kuleuven.be/about/
Formal applications should be sent by email to Hans Op de Beeck, and
should include a scientific CV (mentioning past research positions and
education, and publications), motivation letter, and the names and
contact information of 2 senior researchers that are willing to write a
recommendation letter if necessary (no letters have to be sent yet).
Application deadline is June 20^th 2011.
For further information please contact Hans Op de Beeck
(hans.opdebeeck(a)psy.kuleuven.be
<mailto:hans.opdebeeck@psy.kuleuven.be>), Bert De Smedt
(Bert.DeSmedt(a)ped.kuleuven.be <mailto:Bert.DeSmedt@ped.kuleuven.be>), or
Bart Boets (Bart.Boets(a)ped.kuleuven.be
<mailto:Bart.Boets@ped.kuleuven.be>).
Bart Boets, PhD
Postdoctoral fellow of the Research Foundation - Flanders
Leuven Autism Research Consortium
Child and Adolescent Psychiatry
Herestraat 49 - box 7003, B-3000 Leuven, BELGIUM
Tel. +32 (0)16/ 34.22.45
Fax. +32 (0)16/ 34.38.30
Email: bart.boets(a)ped.kuleuven.be <mailto:bart.boets@ped.kuleuven.be>
--
Gary Green
Dear Users
This Thursday (4-5 pm in YNiC) there will be a YNiC project proposal
presentation given by Chris Racey.
The title of the talk is "The effects of parametrically manipulating view
exposure range on representational invariance in object selective
cortex". Please see the abstract below.
Everyone is welcome to attend.
N.B. The starting time of the YNiC seminars will be 4 pm this term.
Best wishes
Rebecca
*Abstract*
Previously we have carried out two experiments in which view shift
of objects and landscape scenes was parametrically manipulated. In both
experiments participants viewed blocks of stimuli changing in view by 0,
5, 10, and 15°. Different levels of adaptation across these view
shift conditions allow us to derive a measure of view sensitivity for any
given voxel or region. We were able to show variation in the degree of
view sensitivity between category selective regions for both objects and
landscape stimuli. Our previous work has shed new light on how category
specific visual information is processed and represented during
perception. However, it is not yet clear what the effect of object
learning and long term storage is on these ventral stream
representations. Previous research on this issue is limited, and there
have been few studies investigating the effects of prior learning on
neural adaptation.
We aim to apply our parametric manipulation of view shift paradigm
during an encoding experiment with unfamiliar objects prior to scanning.
Participants will under training, and learn to recognise objects where
their range of view exposure will vary parametrically, from 0°,
10°, and 20°. In the scanner, all of the stimuli will be
presented from previously unseen views in an fMR-adaptation block design,
with blocks of images shifting in view in 10° steps. For each
pre-exposure condition, the presentation conditions in the scanner will
be identical, and any differences across conditions must be due to
differences during the encoding of items. We predict that objects learned
with a greater range of views will be associated with richer, more
invariant, representations, and show greater degrees of invariant
adaptation than objects learned under a narrower range of views.
--
************************************************************************
Dr. Rebecca E. Millman Science Liaison Officer York Neuroimaging
Centre The Biocentre York Science Park Heslington YO10 5DG Tel: +44 (0)
1904 567614 Fax: +44 (0) 1904 435356
Hi Everyone,
Due to an important event taking place, please be aware that YNiC will
be closed all day on Friday 27 May and there will be no scanning or
access to the computers. The centre will be closed on Monday 30th due
to the bank holiday and open again as usual on Tuesday 31st May.
Best Wishes
Jen
http://neuroskeptic.blogspot.com/2009/09/fmri-gets-slap-in-face-with-dead-f…
********************************************************************
Philip Quinlan E-Mail: ptq1(a)york.ac.uk
Department of Psychology FAX: (01904) 323181
The University of York Tel: (01904) 320000 Ext. 3135
Heslington Direct : (01904) 323135
York
YO10 5DD
U.K.
********************************************************************
Dear Users
Please do not smoke just outside the entrance to YNiC.
Thank you
Gary
--
Gary Green
York Neuroimaging Centre
The Biocentre
York Science Park
Innovation Way
Heslington
York
YO10 5DG
http://www.ynic.york.ac.ukhttps://www.ynic.york.ac.uk/about-us/people/ggrg
tel. +44 (0) 1904 435349
PA +44 (0) 1904 435329 or reception(a)ynic.york.ac.uk
fax +44 (0) 1904 435356
mobile +44 (0) 788 191 3004
This email to the FSL mailserver list may be of interest to local YNiC
FSL users
Gary
----------------------------------
Dear David,
The short answer is, no, there is no way to justify Z=1.7 as a
cluster-forming threshold in FEAT.
The problem is that the cluster size P-values are based on Random Field
Theory (RFT), and RFT makes various approximation that are only valid
for high thresholds. While one early reference (Petersson et al, 1999)
specified cluster-forming threshold P=0.01 / Z=2.33 as a practical lower
limit for accurate results, later work (Hayasaka & Nichols, 2003; Silver
et al, 2010; K. Worsley personal communication) found even that level
was unstable, and instead recommended P=0.001 / Z=3.09 as a lower limit
on a cluster-forming threshold to ensure accurate inferences.
On the other hand, if you are using randomise, you can safely use any
cluster-forming threshold (though if you go too low, the clusters might
be too extended and spindly to be interpretable). If using randomise,
though, check out TFCE as away to avoid specifying any particular
cluster-forming threshold.
To answer your second question, the cluster-forming threshold used at
lower-levels is only used to make inferences *at* the lower level, and
is ignored at higher levels. Only the cluster-forming
threshold specified in the top-level FEAT analysis matters for the
top-level results.
-Tom
Petersson, K. M., Nichols, T. E., Poline, J.-B., & Holmes, A. P. (1999).
Statistical limitations in functional neuroimaging II. Signal detection
and statistical inference. /Phil. Trans. R. Soc. Lond. B/, /354/, 1261-1281.
Hayasaka, S., & Nichols, T. (2003). Validating cluster size inference:
random field and permutation methods. /NeuroImage/, /20/, 2343-2356.
Silver, M., Montana, G., & Nichols, T. E. (2010). False positives in
neuroimaging genetics using voxel-based morphometry data. /NeuroImage/.
Elsevier Inc. doi: 10.1016/j.neuroimage.2010.08.049.
On Mon, May 9, 2011 at 1:06 PM, David Soto <d.soto.b(a)gmail.com
<mailto:d.soto.b@gmail.com>> wrote:
Hello,
I am finding that when I use a Z<1.7 to define the cluster size at
he highest level analyses, I am getting some interesting activations
in regions that I don't see when I use Z<2.3. In both cases I use
cluster thresholding and p<0.05 whole brain corrected.....
I know the Z value used to define cluster size prior to correction
for multiple comparisons is arbitrary, but is it there any paper
that I can use to justify
in my study why a Z<1.7 was used instead of Z<2.3?
Would it be right to say that poststat results with a Z<1.7 are more
lenient than with a Z<2.3? I feel it this is not necessarily right
but can you please advise?
A second question I have is about poststats as implemented in FEAT....
Say that I have done a lower level analyses - for session, a 2nd
level -across session within subjects- and 3rd level -across subjects-
do I need to set up the Z<1.7 at the first and second level and
third level analyses - or does FEAT bring the unthresholded data
from lower level analyses to the higher levels and then use the Z
score specified at the highest level analyses? in other words, will
I get the same results if I specify
Z<1.7 across all levels or whether I do Z<2.3 for first and second
level and Z<1.7 at the higher level?
Many thanks,
David
--
____________________________________________
Thomas Nichols, PhD
Principal Research Fellow, Head of Neuroimaging Statistics
Department of Statistics & Warwick Manufacturing Group
University of Warwick
Coventry CV4 7AL
United Kingdom
Email: t.e.nichols(a)warwick.ac.uk <mailto:t.e.nichols@warwick.ac.uk>
Phone, Stats: +44 24761 51086, WMG: +44 24761 50752
Fax: +44 24 7652 4532