Hi,
Just a final reminder that tomorrow morning starting at around 9am, the
YNiC desktop, cluster and remote desktop systems will be undergoing
upgrade work. We expect this to be complete by lunchtime, with the
exception of the remote desktop service which may be out of action until
next week.
Thanks,
Mark
--
Mark Hymers
York Neuroimaging Centre
FYI
------------------
We are recruiting MSc and PhD students for a funded MEG study looking at
neuronal connectivity and stroke recovery. Students will have the
opportunity to undergo research through the Depts of Kinesiology or
Psychology/Neuroscience at Dalhousie University in Halifax, Nova Scotia,
Canada.
This research project will capitalize on the spatiotemporal resolution
of MEG to examine changes in connectivity within the sensorimotor
network of individuals post-stroke. Specifically, the goal of this
research is to ‘pave the road to post-stroke rehabilitation’.
Identifying the ‘normal’ sensorimotor network and establishing the
relationship between network re-organization and functional recovery
will permit the development and implementation of treatments to direct
brain recovery. With regard to the proposed research project, and in
groups of non-disabled controls and patients post-stroke, our objectives
include:
1. To establish the connectivity pattern of the ‘normal’ sensorimotor
network and demonstrate the ability to detect changes within the network
using an established motor learning paradigm
2. Using clinical measures of upper limb function, we will establish the
relationship between the pattern of sensorimotor network connectivity
and functional recovery in well and poorly recovered patients
You can find more information at: http://myweb.dal.ca/sh539856/
If interested, please e-mail Dr. Shaun Boe (s.boe(a)dal.ca
<mailto:s.boe@dal.ca>) or Dr. Tim Bardouille (tim.bardouille(a)nrc.ca
<mailto:tim.bardouille@nrc.ca>).
Best,
Tim Bardouille.
---------------------------------------------------------
Timothy Bardouille, PhD, Research Officer
Laboratory for Clinical MEG
NRC Institute for Biodiagnostics (Atlantic)
Office: Halifax Infirmary
3900 - 1796 Summer Street
Halifax, Nova Scotia B3H 3A7
Phone: 902-473-1865
Lab: 902-470-3936
Fax: 902-473-1851
---------------------------------------------------------
FYI
These changes may be important if you are using EEGLAB for multiple
subject analyses
Gary
-------- Original Message --------
Subject: [Eeglabnews] EEGLAB 10.2.5.5 now available - critical upgrade
Date: Tue, 13 Sep 2011 09:43:48 +0200
From: Arnaud Delorme <arno(a)ucsd.edu>
To: eeglabnews(a)sccn.ucsd.edu
Dear EEGLAB users,
New EEGLAB version 10.2.5.5 is now available. This is a critical update
if you are using EEGLAB STUDY sets to process multiple subjects. This
version fixes 3 important problems:
- Plotting ERP and power spectral scalp topographies (a problem that
appeared in EEGLAB 10.2.2.4 two months ago). You will not need to
recompute anything.
- Plotting ERSP data (for independent component clusters and channels)
when a common baseline is being subtracted from the data (not the
default option). You will not need to recompute anything.
- Correctly computing component cluster ERSPs when independent
components were selected using a residual variance threshold. Simply
download the latest version of EEGLAB 10; upon opening a STUDY, a
warning message will appear if you need to recompute ERSPs.
EEGLAB 9.0.8.6 has also been updated. The list of all recent changes are
available at:
http://sccn.ucsd.edu/wiki/EEGLAB_revision_history
We are constantly working on new test scripts to attempt to validate
outputs for complex STUDY structures. Whenever you encounter a problem,
please submit a bug report at http://sccn.ucsd.edu/eeglab/bugzilla.
<http://sccn.ucsd.edu/eeglab/bugzilla>
Thank you for using EEGLAB,
A. Delorme
I have two related but different tasks - task A and task B.
I find that when you do task A regions x, y, z light up and when you do task B regions x, y, z, and w light up.
As we all know all regions of the brain light up to varying degrees regardless what's going on but what I want to be able to demonstrate is that w really is a region unique to task B.
I should add the data for tasks A and B were collected under different conditions so no simple 'contrast' is possible.
Any help gratefully received.
Philip.
********************************************************************
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.
********************************************************************
Hi,
On Friday 23rd September, we'll be upgrading the YNiC desktops and
cluster machines to a new software release. The main changes are:
* FSL 3.3 will no longer be available
* FSL 4.1.4 will be upgraded to FSL 4.1.8
* The default Matlab version will move to 7.12
* python2.5 will move to python2.6 (2.5 will still be available but some
modules may be missing)
Unsupported software changes:
* afni will be updated from 20101222 -> 20110610
* freesurfer 4.5 will no longer be available; 5.1 will be available
instead (although possibly not immediately, we'll announce this at the
time)
This means that on the morning of Friday 23rd, there will be some
disruption at YNiC and the remote desktop service will be unavailable.
It is possible that the remote desktop service will remain unavailable
for a couple of days after the migration in order to give us extra time
to migrate it, although we are aiming to avoid this.
Thanks,
Mark
--
Mark Hymers
York Neuroimaging Centre
FYI
Research assistant, Pittsburgh, Pennsylvania, USA
________________________________________
Employment Type: Full-time 24-month appointment as a Research Assistant
Institution: Department of Neurological Surgery, University of
Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA
Available: September 1, 2011
Job description:
A research assistant position is available with the UPMC MEG Brain
Mapping Center (http://www.meg-brain-mapping.pitt.edu/index.html) at the
University of Pittsburgh Medical Center in Pittsburgh, PA. The research
will consist of using MEG to study the temporal dynamics of how brain
regions interact, both in spontaneously (when people are at rest) and in
the service of visual processing.
Candidates will be expected to:
• Analyze MEG data using advanced mathematical and computational
methods some of which have been developed in house primarily using
MATLAB
• Assist in data collection from healthy volunteers and clinical
groups
• Assist in the preparation of manuscripts
• Work independently and liaise between collaborating laboratories
Qualifications:
• Undergraduate or Masters degree in Psychology, Neuroscience,
Mathematics, Physics, Computer Science, Mathematics, Engineering or
related field
• Strong organizational skills
• Previous experience in computer programming (MATLAB experience
preferred)
• Previous experience in image/signal processing would be highly
advantageous
• Prior experience in neuroimaging data analysis would be a plus
• Prior experience in working with clinical groups would be a plus
Salary: Commensurate with Experience
How to Apply: If interested, please send a CV, cover letter, and names
of references to Dr. Avniel Ghuman, Department of Neurological Surgery,
University of Pittsburgh Medical Center at ghumana(a)cnbc.cmu.edu.
Applications will be considered until the position is filled.
--
Gary Green
Dear YNiC Users,
preparations for the construction of the new Centre for
Hyperpolarisation (CHyM) are scheduled to start with the next week, with
the build anticipated to last for about 10 months. During the course of
the building work the YNiC entrance doors will not be in use and all
users and visitors are therefore requested to access YNiC via the main
BioCentre reception doors.
During the course of the works Claire and I will be in the temporary
YNiC reception office which can be found to the left hand side of the
BioCentre reception desk. Our contact details will remain the same.
The participant forms will not be moved to the temporary office so
anyone needing access to these is requested to see any member of YNiC
staff for assistance. Please continue to drop off participant forms in
the post box.
Further updates about the progress of the building work will be issued
in due course and a display including the building plans can be found in
the BioCentre foyer area.
With best wishes,
Jo.
--
............................
Jo Saunders
Centre Manager
YNiC
The BioCentre
York Science Park
YORK
YO10 5DG
Email: Joanna(a)ynic.york.ac.uk
Tel: (01904) 435343
Fax: (01904) 435356
Tues, Wed & Thurs
.............................
Dear All, please find below the announcement for a PhD studentship in the
University of Milano-Bicocca. Regards, Giulia
University of Milano-Bicocca, Department of Psychology
Four-year Ph.D. Research Studentship
Deadline: October 10th, 2011
A fully-funded Ph.D. studentship beginning in January 2012 for 4 years is
available within the Doctoral School in Psychology and Cognitive Science,
Department of Psychology at University of Milano-Bicocca, Milano, Italy,
for applicants interested in the study of cognitive functions (language,
verbal STM, executive functions) in neuropsychological patients and in
unimpaired subjects by means of TMS, tDCS and fMRI. Also research on deaf
and deafblind individuals is currently performed. These are topics
available in the Doctoral Training Program in "Experimental Psychology,
Linguistic and Cognitive Neuroscience", which has available a total of six
4-year full time studentships. Two summer schools will be also organized.
The successful applicant will have access to all the facilities available
within the TMS-EEG (and EMG) lab at the Department of Psychology, as well
as Eye-Trackers, ERP, fMRI (the latter within a Hospital nearby the
University), neurosurgery patients undergoing awake surgery for tumor
removal and neuropsychological patients in several different hospitals in
MIlano. We encourage application from candidates with a demonstrable
interest in working with patients or with experience on the different
methodologies. Applications are welcome from UK and EU as well as non-EU
citizens. Candidates should have, or expect to get, an undergraduate degree
in Psychology or a related discipline. A Master degree in psychological
research methods or a cognate discipline would be an advantage.
Funding will consist of a monthly salary of approximately 1,170 Euros plus
support for travel and equipment.
The deadline for application is October 10th, 2011. Selection will take
place in the form of a written test and oral colloquium in October.
Information about how to apply can be found at the following links:
- italian version:
http://www.unimib.it/open/news/Bando-XXVII-ciclo-corsi-di-Dottorato-condeco…
- english version: courtesy english translation:
http://www.unimib.it/open/news/Announcements-englishversion/824598639538508…
"Announcement for courses that will begin on 1st January 2012" (page 15 of
the .pdf file).
Enquires about how to apply can be e-mailed to the following address:
phdpsineco(a)unimib.it
Please, feel free to contact prof. Costanza Papagno with questions.
Dipartimento di Psicologia
Università di Milano-Bicocca
e-mail: costanza.papagno(a)unimib.it
Skype: costanza1411
Please feel free to pass this information on to any interested
undergraduate or master student you may know.
Dear Users
Today (4-5 pm in YNiC) there will be a talk by Dr. Peter van Zijl from
Johns Hopkins University and the Kennedy Krieger Institute.
http://www.kennedykrieger.org/kki_staff.jsp?pid=1064
The title of Dr van Zijl's talk is "Chemical Exchange Saturation
Transfer (CEST) contrast agents". Please see below for the talk abstract.
Everyone is welcome to attend and refreshments will be provided after
the talk.
Best wishes
Rebecca
Abstract:
CEST agents1,2 exploit exchangeable protons to achieve contrast in MRI.
This can be
accomplished by using radiofrequency saturation at the NMR frequency of
these protons and
monitoring of the transfer of this saturation to the water protons
imaged in MRI. When
continuous saturation is applied, strong sensitivity enhancements
(factors of hundred to
hundreds of thousands depending on the protons) can be attained to image
micromolar
compounds. CEST agents have been broadly classified in terms of
containing paramagnetic
metals (paraCEST) or not (diaCEST). The main characteristic of diaCEST
agents is that the
chemical shift range of their exchangeable protons is limited to a range
of approximately 6-7
ppm positive with respect to the water signal, which can be extended by
another 6-7 ppm
through hydrogen bonding of the exchangeable site. Currently, protons
used for diaCEST
include OH (hydroxyl, ~0-3ppm from water), NH2 (amine ~0-3 ppm from
water), NH (amide, ~3-
4ppm from water; imino, ~5-7ppm from water). The main compounds are
carbohydrates
(sugars), peptides and proteins, and nucleic acids, which is important
to mention because these
are natural bio-organic substances. MRI is an insensitive method and,
contrary to PET and
optical approaches, the application of contrast agents often requires
physiologically
incompatible (micromolar-millimolar) concentrations. Unlike paramagnetic
metallic contrast
agents, diaCEST provides natural, non-metallic labels. As a consequence,
this methodology
has already allowed the use of many agents in vivo in animals, while
endogenous markers such
as cellular peptides and sugar derivatives are even been studied in
humans. Recent data
suggest that amide proton transfer (APT) may provide a biomarker for
separating tumor
recurrence from treatment necrosis in the brain. ^3
In this presentation, an overview will be given of current diaCEST
agents as well as of
their applications and pitfalls. Based on its non-invasive character,
diaCEST is expected to
revolutionize the rapid translation of contrast agents to the clinic.
The field is evolving rapidly
and many novel exogenous agents and endogenous markers are expected to
be discovered in
the near future.
Reference: 1) Ward KM et al. J Magn Reson 2000;143:79–87. 2) van Zijl
PC, Yadav NN. Magn Reson
Med. 2011;65(4):927-48. 3) Zhou J. et al. Nat Med. 2011;17(1):130-4.
--
************************************************************************
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 *Wednesday* (4-5 pm in YNiC) there will be a talk by Dr. Peter van
Zijl from Johns Hopkins University and the Kennedy Krieger Institute.
http://www.kennedykrieger.org/kki_staff.jsp?pid=1064
The title of Dr van Zijl's talk is "Chemical Exchange Saturation
Transfer (CEST) contrast agents". Please see below for the talk abstract.
Everyone is welcome to attend and refreshments will be provided after
the talk.
Best wishes
Rebecca
Abstract:
CEST agents^1,2 exploit exchangeable protons to achieve contrast in MRI.
This can be
accomplished by using radiofrequency saturation at the NMR frequency of
these protons and
monitoring of the transfer of this saturation to the water protons
imaged in MRI. When
continuous saturation is applied, strong sensitivity enhancements
(factors of hundred to
hundreds of thousands depending on the protons) can be attained to image
micromolar
compounds. CEST agents have been broadly classified in terms of
containing paramagnetic
metals (paraCEST) or not (diaCEST). The main characteristic of diaCEST
agents is that the
chemical shift range of their exchangeable protons is limited to a range
of approximately 6-7
ppm positive with respect to the water signal, which can be extended by
another 6-7 ppm
through hydrogen bonding of the exchangeable site. Currently, protons
used for diaCEST
include OH (hydroxyl, ~0-3ppm from water), NH2 (amine ~0-3 ppm from
water), NH (amide, ~3-
4ppm from water; imino, ~5-7ppm from water). The main compounds are
carbohydrates
(sugars), peptides and proteins, and nucleic acids, which is important
to mention because these
are natural bio-organic substances. MRI is an insensitive method and,
contrary to PET and
optical approaches, the application of contrast agents often requires
physiologically
incompatible (micromolar-millimolar) concentrations. Unlike paramagnetic
metallic contrast
agents, diaCEST provides natural, non-metallic labels. As a consequence,
this methodology
has already allowed the use of many agents in vivo in animals, while
endogenous markers such
as cellular peptides and sugar derivatives are even been studied in
humans. Recent data
suggest that amide proton transfer (APT) may provide a biomarker for
separating tumor
recurrence from treatment necrosis in the brain. ^3
In this presentation, an overview will be given of current diaCEST
agents as well as of
their applications and pitfalls. Based on its non-invasive character,
diaCEST is expected to
revolutionize the rapid translation of contrast agents to the clinic.
The field is evolving rapidly
and many novel exogenous agents and endogenous markers are expected to
be discovered in
the near future.
Reference: 1) Ward KM et al. J Magn Reson 2000;143:79–87. 2) van Zijl
PC, Yadav NN. Magn Reson
Med. 2011;65(4):927-48. 3) Zhou J. et al. Nat Med. 2011;17(1):130-4.
--
************************************************************************
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 Dr Aneurin Kennerley from
the University of Sheffield.
http://www.sheffield.ac.uk/psychology/staff/research/aneurin-kennerley
The title of Dr Kennerley's talk is "Concurrent 7T fMRI and 2-D Optical
Imaging Spectroscopy: Towards building a forward model between neuronal
activity and the BOLD signal". Please see below for the talk abstract.
Everyone is welcome to attend and refreshments will be provided after
the talk.
Best wishes
Rebecca
Abstract:
Functional magnetic resonance imaging (fMRI) has become the cornerstone
of cognitive neuroscience in recent years. The widely used Blood
Oxygenation Level Dependent (BOLD) signal is often used to interpret
changes in neuronal activation. However, at present, a biophysical
understanding of the neurovascular drivers of the BOLD signal is not
clear and thus hinders any quantitative estimation of the underlying
neuronal activity.
Neuroimaging research at the University of Sheffield drives towards
building a forward biophysical model of this complex relationship. As
part of this multidisciplinary group my research is aimed at developing
a general model of the BOLD signal which can model both intra- and
extra- vascular MR signals, across a wide range of imaging parameters,
from estimates of the haemodynamic changes.
Validation and refinement of the haemodynamic response models underlying
fMRI signals, an essential precondition for the correct interpretation
of human BOLD data requires invasive multimodal animal imaging. I have
developed an innovative in-vivo methodology for concurrent fMRI and 2D
optical imaging spectroscopy (2D-OIS) techniques for simultaneous
measurement of BOLD signal and underlying haemoglobin changes to
neuronal activation in the healthy rodent model.
Applications of this technology include: 1) Understanding of the
negative BOLD signal (Boorman et al 2010). Most researchers assume a
negative BOLD to be a result of either neuronal inhibition or vascular
steal. It is only with the simultaneous, independent measurement of
haemoglobin changes (with 2D-OIS) that one could disassociate any
possible physiological relationships; 2) Refinement of mathematical and
biophysical models of both the BOLD signal and optical imaging
spectroscopy techniques (Kennerley et.al. 2009); 3) Calibration of
non-BOLD fMRI techniques such as VASO and ASL; 4) Interpretation of
abnormal BOLD responses; specifically in disease and trauma conditions
in which either neuronal or haemodynamic breakdown could be responsible.
[1] Boorman, L.W. et.al. (2010) /Journal of Neuroscience/. /30(12):
4285-94;/ [2] Kennerley, A.J. et.al (2009) /NeuroImage 47:1608-1619/;
--
************************************************************************
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 Dr Aneurin
Kennerley from the University of Sheffield.
http://www.sheffield.ac.uk/psychology/staff/research/aneurin-kennerley
The title of Dr Kennerley's talk is "Concurrent 7T fMRI and 2-D Optical
Imaging Spectroscopy: Towards building a forward model between neuronal
activity and the BOLD signal". Please see below for the talk abstract.
Everyone is welcome to attend and refreshments will be provided after
the talk.
Best wishes
Rebecca
Abstract:
Functional magnetic resonance imaging (fMRI) has become the cornerstone
of cognitive neuroscience in recent years. The widely used Blood
Oxygenation Level Dependent (BOLD) signal is often used to interpret
changes in neuronal activation. However, at present, a biophysical
understanding of the neurovascular drivers of the BOLD signal is not
clear and thus hinders any quantitative estimation of the underlying
neuronal activity.
Neuroimaging research at the University of Sheffield drives towards
building a forward biophysical model of this complex relationship. As
part of this multidisciplinary group my research is aimed at developing
a general model of the BOLD signal which can model both intra- and
extra- vascular MR signals, across a wide range of imaging parameters,
from estimates of the haemodynamic changes.
Validation and refinement of the haemodynamic response models underlying
fMRI signals, an essential precondition for the correct interpretation
of human BOLD data requires invasive multimodal animal imaging. I have
developed an innovative in-vivo methodology for concurrent fMRI and 2D
optical imaging spectroscopy (2D-OIS) techniques for simultaneous
measurement of BOLD signal and underlying haemoglobin changes to
neuronal activation in the healthy rodent model.
Applications of this technology include: 1) Understanding of the
negative BOLD signal (Boorman et al 2010). Most researchers assume a
negative BOLD to be a result of either neuronal inhibition or vascular
steal. It is only with the simultaneous, independent measurement of
haemoglobin changes (with 2D-OIS) that one could disassociate any
possible physiological relationships; 2) Refinement of mathematical and
biophysical models of both the BOLD signal and optical imaging
spectroscopy techniques (Kennerley et.al. 2009); 3) Calibration of
non-BOLD fMRI techniques such as VASO and ASL; 4) Interpretation of
abnormal BOLD responses; specifically in disease and trauma conditions
in which either neuronal or haemodynamic breakdown could be responsible.
[1] Boorman, L.W. et.al. (2010) /Journal of Neuroscience/. /30(12):
4285-94;/ [2] Kennerley, A.J. et.al (2009) /NeuroImage 47:1608-1619/;
--
************************************************************************
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
Some users may need to be aware of this particular bug in EEG.
--
Claire Fox
PA to Professor Gary Green
The York Neuroimaging Centre
Innovation Way
Science Park
York
YO10 5DG
Tel: 01904 435329
Fax: 01904 435356
Email: Claire.fox(a)ynic.york.ac.uk
FYI
---------------------------------------
Dear colleagues,
We would like to invite you to contribute your research to our special
issue on the role of brain oscillations in language processing, to
appear in Frontiers in Language Science.
You can visit the web site at:
_http://www.frontiersin.org/languagesciences/specialtopics/brain_oscillatio…
See detailed description below.
The call has been very successful so far and prominent figures in the
field have joined us in this project.
We are looking forward to receiving your research.
Best wishes,
Lucia Melloni & Marcela Pena
*Brain Oscillations during Language Processing: from Perception to
Production *
/Deadline for abstract submission: 01 Sep 2011 /
/Deadline for full article submission: 15 Dec 2011 /
Language processing is a seemingly effortless task that requires the
integration of speech units (e.g., phonemes, syllables, words, etc.)
occurring at different rates. In particular, temporal binding for speech
should occur within and across different temporal scales, necessitating
multiple simultaneous windows of integration for prosodic, semantic,
syntactic and pragmatic processing. Recent evidence suggests that
neuronal oscillations may reflect both tracking linguistic units at
their individual rhythms as well as integrating speech units over a
large range of temporal scales.
The present Research Topic would like to evaluate current theories and
evidence for a mechanistic role of neuronal oscillations in measuring
language processing, covering the latest advances brought about by EEG,
MEG and fMRI imaging methods. Our main focus is to highlight innovative
and foundational studies that go beyond methodological issues and
advance our theoretical understanding of the role of brain oscillations
in language processing. Contributions from the pioneers of this field
are selected, illustrating how the study of brain oscillations has
allowed investigating theoretically relevant questions that could not be
addressed by more traditional methods. The topic thus aims at deepening
our mechanistic understanding of language processing and bringing us
closer to bridging the gap between brain, mind and behavior for the
crucial cognitive function of speech.
Hosted By:
Marcela Pena <http://www.frontiersin.org/people/MarcelaPena/5634>,
Catholic University of Chile, Chile
Lucia Melloni <http://www.frontiersin.org/people/LuciaMelloni/32689>,
Max Planck Institute for Brain Research, Germany
------------------------------
Lucia Melloni, Ph.D
Max Planck Institute for Brain Research
Deutschordenstr. 46
60528 Frankfurt am Main
Germany
lucia.melloni(a)brain.mpg.de <mailto:lucia.melloni@brain.mpg.de>
T: +49 69 96769-268 <tel:%2B49%2069%2096769-268>
F: +49 69 96769-327 <tel:%2B49%2069%2096769-327>
--
Gary Green
Dear all,
for the few of you who wanted to follow up some of the references from my
talk today, I've put the presentation here:
/groups/resources/hbmReview.pptx
Some of the videos probably won't work, so I've added links to where they
may be accessed.
Michael
FYI
-------- Original Message --------
To Whom it May Concern:
ATR Neural Information Analysis Laboratories, Kyoto, Japan, have
openings for researcher positions and invite applications from
Ph.D. holders (or Ph.D. candidates who are very close to completion)
with strong motivations and ambitions in the research project
described below.
Our institute ATR, located in western Japan, is one of the top
research centers in computational neuroscience, biomedical signal
processing, and robotics in Asia (see http://www.cns.atr.jp/en/ for
more details). Our group research on brain-machine interface (BMI),
which controls actuators by estimating human movement and intension
from brain activities measured noninvasively by MEG, EEG, fMRI, and
NIRS. In particular, we focus on developing information scientific
methods, bio-measurement techniques, and neurosciences.
The project for which we are recruiting aims to construct a new
information-communication technology to connect people and machines
through engineering applications of neuroscience. More specifically,
the project's goal is to develop a BMI methodology that works well in
various environments in the real world by simultaneous measurement of
human behavior and brain activities and also by parallel and
distributed processing of large-scale data.
We look forward to your applications and recommendations.
Shin Ishii
ATR Neural Information Analysis Laboratories, Kyoto, Japan
= Job description =
(1) Ambient informatics team
The researcher will join a team dedicated for establishing an
environment for continuous measurement and recognition of human
behavior in a daily life. Here, the "environment" includes hardware
facilities, efficient network, and pattern recognition algorithms and
software. The team is supported by engineers. Data measurement
devices include stereo cameras, laser range finders, microphones,
pyroelectric sensors, power monitors (for appliance), and
bio-measurement devices (for electromyogram (EMG), heart pulse, blood
pressure, perspiration, and temperature). Good proposals for
additional measurement modalities will be welcomed.
(2) Decoding team
The researcher will join a team dedicated for developing artifact
reduction and decoding algorithms for brain activities measured under
real environments. Brain activity data measured in real environments
would often be contaminated by non-brain signals, which must be
reduced by all means for further analysis. By solving a challenging
research problem of decoding of movement or intension in uncontrolled
experiments, the team will develop BMI algorithms under real
environments. The successful candidate should have a strong
background in machine learning, information retrieval, or statistical
signal processing. Excellent programming skills and experiences of
large-scale data analysis will be advantageous.
(3) Neurosciences team
The researcher will join a team dedicated for neuroscience studies
focusing on human decision making and motor control under real
environments. The team's challenging goal is to elucidate the neural
bases involved in decision making and motor control, which are
sufficiently robust even in the uncertain real world, by fully
utilizing newly developed techniques of brain machine interface.
The teams include several foreign researchers and we also have
collaborated closely with researchers in countries overseas. Thus,
applications from abroad are particularly welcome.
= Requirements =
Applicants must:
- have a Ph.D. (or be near completion).
- have strong motivations and ambitions to take part in the research above.
Also, researchers having interest in neural and human science with
expertise in one or more of the following areas are welcomed:
- Statistics, machine learning, parallel distributed computing, signal
processing, artificial intelligence, bio-measurement and
instrumentation, computer vision, statistical physics, cognitive
psychology.
Exceptional applicants with a master’s or equivalent degree will be
considered as well.
= Number of openings =
Few
= Employment conditions =
Position : Full-time Researcher / Full-time Research Engineer
Tenure : Single year based contract, renewable based on evaluation
Treatment: Based on individual performance
Work Location:
Advanced Telecommunications Research Institute International (ATR)
2-2-2 Hikaridai, Seika-cho, Soraku-gun, Kyoto 619-0288, Japan
= Application materials =
Please submit the following five materials to the contact address
below, either in printed or electronic form:
1. CV
2. List of publications
3. Reprints of 1–3 major publications
4. Document (one or two pages in A4 or letter size) describing:
- Summary of your previous research
- Interests and proposal for research
- Additional research skills not directly foreseeable from publications
5. Recommendation letters from two researchers
* Original documents you submit will not be returned.
= Judging system =
After documentary examination, we ask for presentation and interview
if needed
= Starting date =
After October 2011 (negotiable)
= Deadline for application =
Opens until positions are filled.
= Contact =
ATR Neural Information Analysis Laboratories
(Application for Researcher Position)
2-2-2 Hikaridai, Seika-cho, Soraku-gun, Kyoto 619-0288, Japan
Email: dbi-info(a)atr.jp
= Use of personal data =
All personal data received will be properly managed and only be used
for the purpose of recruitment.
--
Gary Green
Dear Users
This Thursday (4 pm in YNiC) Michael Simpson will give a review of the
recent Human Brain Mapping meeting.
Everyone is welcome to attend and refreshments will be served afterwards.
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
Together with Andre and Nikos, we have collected some potentially very
interesting results via an fMRI study on task switching.
The issue is this. When we do group analyses with cluster correction,
3 very large blobs are found in contrasting cond 1 with cond 2.
However, in playing with fslview it is clear that within these blobs
there are more interesting localised islands of activity.
My dilemma is this if we simply report the cluster-corrected blobs
that is okay but what
I really want to discuss are these other ROIs.
So how do I get this published and satisfy the statisitcal reviewer?
I cannot do a simple a priori ROI analysis because some of the
conditions are relatively novel and we cant predict where the ROIs
might be.
We can do this via email or I can talk about this at YNiC next week
perhaps?
Philip.
********************************************************************
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.
********************************************************************
FYI
-------------------
A postdoctoral position is available for up to 3 years for a cognitive
neuroscientist interested in the functional and neural basis of
attention, control, and learning. The successful candidate will work on
a BBSRC-funded project investigating the role of action outcomes in
cognitive control, using fMRI, EEG, and behavioural methods.
The research will be conducted in Oxford as part of a new collaboration
between Dr Nick Yeung, in the Dept of Experimental Psychology at Oxford,
and Dr Florian Waszak, in the Laboratoire Psychologie de la Perception
at the Universite Paris Descartes. We offer an international research
environment and the opportunity for the successful applicant to develop
skills in a broad range of complementary methods in cognitive neuroscience.
For more information about the post, including instructions on how to
apply, please visit:
http://www.recruit.ox.ac.uk/pls/hrisliverecruit/erq_jobspec_version_4.jobsp…
Or contact Nick Yeung at nicholas.yeung(a)psy.ox.ac.uk
Further information about Yeung and Waszak's labs can be found at:
http://psyweb.psy.ox.ac.uk/acc/http://lpp.psycho.univ-paris5.fr/person.php?name=FlorianW
The closing date for applications is August 26, 2011.
--
Gary Green
Dear all,
just to let you know that there will be a school visit in YNiC from
10.00 until 11.15 tomorrow, July 20th. No workstations will be used,
however the presentation area will be being used. Therefore, Open Plan
will be busier than usual, and there will no doubt be a greater level of
background noise ...
Michael
--
Dr Michael Simpson
Science Liaison Officer
York Neuroimaging Centre
Innovation Way
York
YO10 5DG
Tel: 01904 567614
Web: http://www.ynic.york.ac.uk
I would like to thank everyone in Psychology, the YNiC-Users and the
YNiC Staff for all their contributions to celebrating the award of an
honorary doctorate to Karl Friston.
He asked me to pass on his additional appreciation to those of you who
contributed to the absolutely fabulous workshop in the Venables Room
yesterday. He was full of praise for the studies being undertaken and
for the excellent talks. He kept referring to the work for the rest of
the day and clearly took away some very strong impressions of the
research being carried out in Psychology.
I would also like to personally thank Claire Fox for her calm,
professional and wonderful organisation of all the events that were
associated with Karl Friston's visit.
Thank you all - we should do it again!
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 - 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 All,
Thanks to those who attended the reception at YNiC for Colin yesterday.
There was a really nice buzz about the place. Thanks particularly to those
who showed Colin around and demonstrated the different techniques we have at
YNiC. It gave an excellent (and correct) impression of the great research
that is taking place. Finally, thanks to Pete, Gary and Quentin for their
anecdotes and tributes to Colin and to Claire for organizing the event so
brilliantly.
Best wishes,
Tim
From: Tim Andrews [mailto:t.andrews@psych.york.ac.uk]
Sent: 13 July 2011 14:59
To: 'all(a)psych.york.ac.uk'; 'ynic-users(a)ynic.york.ac.uk'
Subject: Colin Blakemore - champagne reception at YNiC
Dear All,
Professor Colin Blakemore FRS will be receiving an honorary degree from the
University tomorrow (Thursday). Some of us have been directly influenced by
Colin's research, but many of you will be more aware of Colin's contribution
to the public understanding of science
http://www.neuroscience.ox.ac.uk/directory/colin-blakemore. To recognize
Colin's achievements, the Department will be holding a champagne reception
at YNiC around 3.20-3.30 tomorrow in the open plan area. There are a few of
us who know Colin well and we will say a few words about him. Quentin will
then say a few words about Colin's contribution to the MRC and his role more
generally in communicating the importance of science to the public.
You are all welcome to come to this event. It is only for a short time, so
please try and come if you can. It would also be great to see some younger
faces. If you are intending on coming, can you please email Claire Fox at
YNiC.
Best wishes,
Tim
--
Dr Tim Andrews
Department of Psychology
University of York
York, YO10 5DD
UK
Tel: 44-1904-434356
Fax: 44-1904-433181
http://www-users.york.ac.uk/~ta505/