Thursday, 10 January 2013

Becoming an MR Operator

We encourage regular users of MR in CUBRIC to become approved operators of the MR scanner.  This not only gives users a better understanding of the way that MR data are acquired, but also allows users greater flexibility in booking scanner time, once they have completed the approval process.

Should I become an MR operator?

It will typically take approximately 20 hours of  training/experience to become an MR operator, but this will vary according to the individual.  Thus, it is not an efficient use of time to train all researchers to operate the scanner.  Whether it is worthwhile for a researcher to train to become an MR operator depends on a number of factors, such as prior experience and the number of hours of scanning you are expecting to perform.  However, PhD students (who do not have separate funding for their studies) will be required to learn to operate the scanner during their time at CUBRIC.
In general, training will take place during the researcher's first study, so it is not nescesary to become an MR operator prior to this.  
Applications for MR operator training should be made to John Evans ( evansj31 AT cf.ac.uk ), using the  MR Operator Training Application Form. Applications for students should be sent by their PhD supervisor.

Requirements

In order to become an MR operator (or 'Approved Users' in the terminology of the CUBRIC Rules and Procedures), the researcher must demonstrate that they can;
•   competently perform the safety screening of participants.
•   safely place participant in the scanner.
•   communicate the important aspects of the scan to the participant both before and during the scan.
•   test the important safety equipment, prior to scanning (e.g. squeeze ball).
•   recognise common scanner faults.
•   correctly prescribe and inspect the scans they perform
•   recognise common artefacts
•   understand the causes of alarms in MR suite
•   can safely remove an unconscious participant from the magnet room.

The minimum requirement for becoming an approved operator is;
1) Attend the MR safety lecture (Contact Peter Hobden, email: hobdenp AT cf.ac.uk )
2) Complete the MR safety test. (Contact Peter Hobden, email: hobdenp AT cf.ac.uk )
3) Observe two sessions run by an MR trainer (one of the experienced MR operators, see list below).  Contact the trainer directly to arrange this.
4) Operate the scanner for (at least) eight sessions, under the supervision of an MR trainer.
5) Complete final approval session with John Evans ( evansj31 AT cf.ac.uk )
All of these should be logged in the MR Operator Training Record

MR Trainers

John Evans
Peter Hobden
Derek Jones
Krish Singh
Martin Stuart
Richard Wise



Wednesday, 15 August 2012

MRS Voxel Registration

This describes the process of localising the actual voxel location used during the acquisition onto the participants FSPGR scan.  The output is a binary voxel mask, in the space of the FSPGR.   This can then be combined with outputs from segmentation (Fast) to calculate the tissue composition of the voxel (wm, gm, csf)

1) Copy native FSPGR dicoms

A copy of the native dicom files (dcm) is required as these contain the position information of the slices in the FSPGR.  The step to create the nifti removes these, so first a copy of the FSPGR dicoms should be made, e.g from the directory of the scan data;
cp Series_0000n FSPGR_dcm_folder
where n is the series number of the FSPGR.

2) Create FSPGR nifti

Then you need to create the FSPGR: go into the Series_0000n folder that contains the FSPGR scan by typing;
geprepfunct 172 1 [name of FSPGR]. 
 e.g.type:  geprepfunct  172  1 Subject1_FSPGR.nii.gz


3) Run VoxelOnFSPGR

Then, in Matlab, run the following function:

VoxelOnFSPGR(pfile, ImagingDataDirectory, MRS_Rot_folder,... FSPGR_dcm_folder, FSPGR_nifti)

VoxelOnFSPGR is in the same location as Gannet, so ensure that you have Gannet in your matlab path for this to work (/cubric/software/Gannet/GannetExtras).
e.g.
 VoxelOnFSPGR( ...
'~/mrs/somato_motor/data/3143_6_P12800.7', ...
'/cubric/home/sapje1/mrs/somato_motor/3143_081007-1', ...
 'Series_00005', ...
 'Series_00004_bak', ...
'fspgr.nii.gz')
Pfile = full path to pfile (e.g. '~/mrs/somato_motor/data/3143_6_P12800.7')

ImagingDirectory = the directory containing imaging data, unpacked by sortdicomball.  The directory '/cubric/home/sapje1/mrs/somato_motor/3143_081007-1' in the above example should contain the Series_00001, ... directories and the nifti FSPGR.

MRS_Rot_folder = folder containing the rotator/oblique localiser scan for the voxel, path from ImagingDirectory (e.g. ‘Series_00005’)

FSPGR_dcm_folder = folder containing the FSPGR native dicom files (e.g. Series_00004_bak')

FSPGR_nifti = the name of the FSPGR you created (e.g. ‘fspgr.nii.gz’)

This will create a voxel mask, in the FSPGR space, for the MRS voxel  and place it in a created directory named MRSVoxelReg. The filename is examnumber_series_Mask.nii.gz so e.g. 3999_08_Mask.nii.gz.

Below is a the output from VoxelOnFSPGR (e.g. 3999_08_Mask.nii.gz, but from an occipital voxel in this case) overlaid on the participant's FSPGR.





Wednesday, 8 August 2012

Scanner Sounds

We have recorded the sounds of a number of the most common sequences run at CUBRIC, which may be useful in acclimatising participants to the noise of a scan.

All of the WAV files are available here , and the sequences available are;

ASL-quipssIOP.wav (Perfusion, IOP)
ASSET.wav
B0map.wav (Fieldmap)
Coldhead.wav (Magnet room background noise)
DESPOT-IRSPGR.wav
DESPOT-SPGR.wav
DESPOT-SSFP.wav
DTI.wav
EPI.wav (fMRI)
FSE-B1map.wav
FSE.wav (T2 Fast Spin Echo)
FSPGR.wav
Localiser.wav
MRS-MEGAPRESS.wav (MEGA-PRESS GABA spectroscopy)
Prescan.wav (run before each separate sequence)
qMT.wav (quantitative MT)





Saturday, 14 July 2012

Transferring MRI data

1) Transferring from the scanner

On the scanner console, when all images in an exam have been collected and you are removing the participant from the scanner, make sure you press the "End Exam" button. This guarantees that all the images you require have been finally written to the internal GE database. Then, from a terminal window in the console, type; copydicom The copydicom script will get run overnight by the scanner, but it is good practice to transfer the data as soon as the exam is finished.
 The script will identify any MRI exams that have not previously been transferred to the CUBRIC cluster file-system (such as the one you have just collected). Note that the exam must be finished before you press this button. Otherwise, additional copies of the exam will end up in the database - which can cause confusion (but will only lead to duplication, rather than a loss of data).
When the command has finished, your images have been packaged up and transferred to the CUBRIC cluster file-system. Note: A typical fMRI experiment may consist of several tens of thousands of images. In the standard DICOM database, each of these images are stored in a separate file. This can be very inefficient, both in terms of file transfers and load on the linux file-system. So, we have taken the decision to package up all the images from an Exam in a single archive file, which is also compressed.  In CUBRIC parlance, this is known as a dicball/tarball.

2) Unpacking Scanner DICOM data

(Note, steps 2 and 3 can be done using the Studies database https://studies.cubric.cf.ac.uk).

Log in to your normal user account on the CUBRIC  system. All dicballs are transferred to the same location, namely: /cubric/mri/direct_transfer/YYYY
where YYYY represents the year of the scan. Dicballs have fairly obscure names, which contain the name and time that the exam started. If you type the following command you will see all the  dicballs currently in the database, sorted so that the last file listed is the last one to be transferred. ls -lrt /cubric/mri/direct_transfer/2012
Here is a typical listing from our database:

2012-07-19-16-35-54-e2357712.tgz
2012-07-19-18-21-53-e2390174.tgz
2012-07-20-08-02-36-e2404155.tgz
2012-07-20-08-08-30-e2404166.tgz
2012-07-20-09-04-34-e2404178.tgz
2012-07-20-10-02-49-e2404274.tgz

To locate a dicball based on the Exam number, use  seriesinfo
e.g.
sapje1@daws15:/cubric/users/sapje1$ seriesinfo 9319
------------------------------------------------------------------

                   REL Study ID//9319 (Exam No)
             DICOM Data Tarball//2013-07-22-08-13-44-e4568456.tgz
               PAT Patient Name//dailyqa 
          PAT Patient Birthdate//
            ID Acquisition Date//20130722
            ID Acquisition Time//075619
              ACQ Protocol Name//dailyQA_2012b/1 
1 // fgre // loc
2 // fgre // ASSET cal
3 // epiRT // EPI TR=3 64x64, 360FOV,no ASSET, no FATSAT
4 // epiRT // EPI QA 10min
------------------------------------------------------------------
This lists the tarball name, time, date and participant ID, and limited information about the series run during the acquisition (pulse sequence name and series description).

3) Unpacking a dicball
 Once you have found the you file you need to unpack, you next have to decide where you want to put the unpacked and processed data. Let's suppose you are doing a project on Widget Perception and the dicball contains data from your subject 23. In your home directory, you probably want to create a directory called Widget, and then sub-directories called Subject23 etc. i.e.:
mkdir Widget
cd Widget
mkdir Subject23
cd Subject23

Now you are in the new directory, you can unpack the dicball using the sortdicomball command. sortdicomball  e.g.
sortdicomball /gpfs/mri/direct_transfer/2007/2007-12-11-10-38-33-e99743.tgz .  
(don't forget the trailing full stop)

This will unpack the selected dicball archive into the current directory. It will create a new sub-directory based on the patient and exam id. If you cd into this, you will see a set of subdirectories e.g.: Series_00001    
Series_00002    
Series_00003 .......

Remember : you need to give the full path to the location of the dicball! 

Alternatively, you can use  tarball.unpackdicom
e.g.
tarball.unpackdicom /cubric/mri/direct_transfer/2013/2013-07-29-15-54-26-e5048388.tgz
(note this unpacks to current directory, and no trailing full stop)
This names the series directory according to the series number + pulse sequence.
e.g. 
1_fgre
2_fgre
3_efgre3d
403_epi2cje032
4_epi2cje032

 4) Converting Dicom data to NIFTI/Analyze format

Each of the above sub-directories contains the Dicom files for one of your series, which you now need to convert into NIFTI files for analysis. Let's suppose Series_00003 contains the data for a functional experiment in which there are 37 anatomical slices collected every TR for 200 volumes.
Here's how you would convert the data using the command geprepfunct:
cd Series_00003
geprepfunct 37 200 widget_sub23_run1
This will create a 4D NIFTI file, called widget_sub23_run1.nii.gz , suitable for analysis with FSL or CUBRIC's other software packages.
You need to change the 3 parameters on the geprepfunct command line to match your data. 
Alternatively, if you can't do the sums to work out number of slices/volumes, use dcm.geprepauto which gets the number of slices from the dicom header, and calculates the number of volumes based on the total number of images in the directory.
e.g.
dcm.geprepauto widget_sub23_run1

5) Converting Structural (FSPGR) data for MEG or FreeSurfer 

Note that, for the analysis of anatomical data to be used for MEG or , we no longer recommend the use of geprepfunct. If your data is a MEG anatomical scan (i.e. one volume) you should instead use the dic2mri command. Note that the dicom files for the series will be packed up into an archive called sorted.tar.gz in the Series_XXXXX sub-directory. Note that these are a copy of the original dicom files stored in the dicball. As such you can go ahead and delete sorted.tar.gz, when you feel ready and comfortable!
One data management strategy that seems to work well is to create a directory, at the same level as the Series_XXXX directories, to hold all your NIFTI files. You can then move all the NIFTIs to this subdirectory using the following:
mkdir NIFTI
mv Series_*/*.nii.gz NIFTI/
Importantly, the NIFTI files must all have different filenames, or they will overwrite each other. Now you are ready to do your analysis...
Note: geprepfunct only generates NIFTI files if this is the default output type for FSL. If the FSLOUTPUTTYPE environment variable is set to ANALYZE, then this is the type of file that will be created. CUBRIC users have NIFTI set to be the default. Converting to Anatomical scans for MEG Follow the Instructions above on using sortdicomball/whodicball Find the dicom series with about 170 .dcm files..this is probably the anatomical scan.
Then run the dic2mri command in that directory. If you have queries about the commands mentioned here, you should contact the authors: copydicom.sh : Spiro lastdicball: Krish whodicball: Krish sortdicomball: Krish geprepfunct: Krish dic2mri: Krish

Monday, 25 June 2012

EPI Unwarping with Fieldmaps


Using fieldmap acquisitions, one can improve the registration of EPI (functional) data to the subject's structural scan.

Preparing Fieldmap Data

The script fmap, which processes the fieldmap data to produce the appropriate files required by FEAT.  The fieldmap acquisition on the CUBRIC scanner comprises of two SPGR scans with different echo times (7ms and 9ms).  The syntax for fmap is;
fmap (fieldmapoutputdir)where fmap1 is the TE=7ms acquisition and fmap2 is the TE=9ms acquisition.  fieldmapoutputdir is the name of the directory where the fieldmap data will be written, this is optional, and the default directory name is fieldmap.

From these SPGR scans fmap produces a fieldmap directory containing the following files;
abs_image_brain_mask.nii.gz:
abs_image_brain.nii.gz: Required by FEAT
fieldmap_rad_s.nii.gz: Required by FEAT

fieldmap_uT.nii.gz
phasediff_brain.nii.gz
phasediff.nii.gz

Check the fieldmap_rad_s image using fslview.  It should appear something similar to the images below, with values typically in the range -2000 to +2000.

Unwarping EPI data within FEAT

On the Pre-stats tab select B0 unwarping with the following parameters;
Fieldmap: the appropriate fieldmap_rad_s.nii.gz file.
Fieldmap map: the appropriate abs_image_brain.nii.gz file.
EPI echo spacing (ms): 0.32
EPI TE (ms): 35
Unwarp direction: +y
% Signal loss threshold: 10

When unwarping is complete, additional data appear in the Pre-stats section of the FEAT report.  Check the quality of the unwarping by looking at the original and unwarped EPI, and the magnitude image of the fielmap data (a low resolotion structural scan).  These are all in the whatever.feat/unwarp directory
EF_D_example_func.nii.gz:  Original ("distorted") EPI volume
EF_UD_example_func.nii.gz: Unwarped (or "undistorted") EPI image
EF_UD_fmap_mag_brain.nii.gz: Structural image (from fieldmap).
The unwarped image (EF_UD_example_func.nii.gz) should be a better match to the structural image than the original (EF_D_example_func.nii.gz).  Look for artefacts in the unwarping, which may be caused by head motion during the fieldmap, or in between the fieldmap and the epi acquisition.


Images (right) show the typical effect of unwarping on EPI data.  Original (red) and unwarped (blue) EPI images are overlaid on top of the fieldmap structural image.  Original EPI shows stretching of data in the anterior direction near the frontal pole (A, B), and a movement of the cerebellum and spinal cord in the posterior direction (C).  These are corrected in the unwarped version (blue)

Sunday, 24 June 2012

Summary Parameters of Standard Scans

MEG FSPGR - Suitable for MEG/fMRI/Retinotopic/mri3dX
3D FSPGR Oblique-Axial
resolution: 1mm isotropic matrix 256x256x176,
field of view 256x256x176
TR/TE=7.9/3.0 ms
TI=450ms
Flip angle=20deg
1 NEX (acq time ~ 10min)

Quick FSPGR - Suitable for MEG/fMRI/Retinotopic/mri3dX
3D FSPGR Oblique-Axial
resolution: 1mm isotropic matrix 256x192x176 (zero-padded to 256x256x176),
field of view 256x192x176mm
TR/TE=7.9/3.0 ms
TI=450ms
Flip angle=20deg
1 NEX (acq time ~ 7min)

High-Resolution FSPGR - NOT suitable for mri3dX/MEG/Retinotopic
3D FSPGR Oblique-Axial
resolution: 0.8mm isotropic matrix 320x320x194 (zero padded to 512x512x194)
field of view 256x256x155mm
TR/TE=7.9/3.0 ms
TI=450ms
Flip angle=20deg
1 NEX (acq time ~ 10min)

30 direction DTI Oblique-Axial.
(ACPC)
TR/TE=Cardiac Gated/87ms (effective)
FOV: 23cm
Acquisition matrix: 96x96
Slice Thickness: 2.4mm 60 slices
30 directions, 3B0.
Parallel acceleration (ASSET) factor=2
 (acq time~13mins)

60 direction DTI Oblique-Axial. (ACPC)
TR/TE=Cardiac Gated/87ms (effective)
FOV: 23cm Acquisition matrix: 96x96
Slice Thickness: 2.4mm
60 slices 60 directions, 6B0.
 Parallel acceleration (ASSET) factor=2
(acq time~25mins)

3.4mm Isotropic GRE-EPI (for fMRI) An fMRI data set was acquired using Gradient Echo-EPI with the following parameters; TR/TE=3000/35 ms, flip angle=90deg, acquisition matrix=64x64, field-of -view=22cm.  53 slices of thickness 3.4mm were acquired, orientated parallel with each subject's ACPC line (oblique-axial).  A parallel acceleration (ASSET) factor of 2 was used.