
This step-by-step guide is for MRI students, radiographers and technologists who wish to improve their planning skills and master the routine brain MRI protocol.
What you will learn:
A routine brain MRI is one of the most requested protocols, so short scan time is often crucial. Most brain pathologies are identified by signal differences, making strong SNR essential. For smaller lesions, higher resolution is needed.
These sequences give fast, high-quality images with strong contrast and relatively few artifacts, which makes them well suited to routine clinical imaging. They let us produce T1 and T2 contrast, and to add an inversion pulse that nulls CSF signal for FLAIR. Together, these help us assess brain structure and detect abnormalities.
| Artifacts | Solution – How to Avoid It |
|---|---|
| Motion artifacts | Shorten the scan time to reduce the risk of patient movement. |
| Susceptibility artifacts | Use spin echo instead of gradient echo sequences to reduce sensitivity to magnetic field inhomogeneities. |
| Chemical shift artifacts | Increase the bandwidth to reduce the spatial displacement between fat and water signals. |
| CSF flow artifacts | Use flow compensation gradients to correct CSF-related phase shifts. FLAIR also reduces this artifact by nulling the CSF signal itself. |
| Truncation artifacts | Increase the resolution to capture more frequency information and reduce Gibbs ringing at tissue boundaries. |
| Wrap-around artifacts | Activate fold-over suppression to prevent anatomy outside the field of view from overlapping. |
The brain is a complex organ responsible for controlling all body functions, processing sensory information, and enabling cognitive abilities. Because of its importance and the range of pathologies that affect it, the brain is one of the most frequently examined areas in MRI.
Brain MRI protocols are used to diagnose a wide range of neurological conditions, including tumors, strokes, multiple sclerosis, as well as psychiatric disorders that affect the brain’s function.

In MRI, we always face a trade-off between 3 key metrics:
Improving one of these metrics reduces the performance of the others. To decide what trade-offs to make, we must consider the needs of each clinical situation.
For routine brain MRIs, it’s generally true that:
Therefore, we typically 1) prioritize scan time, 2) maintain good SNR for clear contrast between tissues, and 3) optimize for resolution when finer details must be assessed.

The brain MRI study can help us diagnose a wide range of health conditions. The table below lists some of the most common conditions, and what pulse sequences that reveal them:
| Common Brain Conditions | Clearly Seen on Sequence | Why This Sequence? |
|---|---|---|
|
Anatomical structures and lesions: • Tumors • Subacute hemorrhage • Metastases • Bone marrow changes |
T1 TSE | Provides clear gray-white differentiation and baseline for contrast assessment. Detects T1 hyperintense findings like subacute hemorrhage and marrow pathology. Contrast-enhanced T1 improves tumor and metastasis visibility. |
|
Edema and fluid abnormalities: • Hydrocephalus • Cysts • Subacute stroke • Tumor-associated edema |
T2 TSE | Highlights water-rich tissues, making it ideal for detecting edema, inflammation, and CSF-related abnormalities. Helps assess fluid accumulation and tissue changes. |
|
White matter and ischemic lesions: • Multiple sclerosis (MS) • Small vessel disease • Chronic ischemia • Gliosis |
T2 FLAIR | Suppresses CSF signal while preserving sensitivity to pathological water, making white matter lesions highly visible. Ideal for detecting demyelination, chronic ischemia, and gliosis, especially near ventricles where bright CSF on T2 could obscure lesions. |
|
Acute ischemic changes: • Acute stroke • Cytotoxic edema • Early infarcts |
Diffusion-Weighted Imaging (DWI) | Detects restricted water molecule movement in acute ischemic tissue within minutes of onset, long before other sequences. It’s the core sequence for rapid stroke treatment decisions. |
The step-by-step guide below will show you how to set up and perform a routine brain MRI protocol in practice.
We will perform the protocol in 3 parts:
Lay the patient head-first and supine (on their back) with the head centered at the scanner's isocenter.
Use a dedicated head coil. It gives strong signal reception and full coverage of the brain, which is what leaves enough SNR to afford high in-plane resolution.
✅ Correct Patient Positioning:

Once the patient is in place, review your scanner’s hardware settings.
In this guide, we will use the following settings:
| Scanner Setting | Value | Why This Value |
|---|---|---|
| Magnetic field strength | 1.5 T | Enables high Signal-to-Noise Ratio, which gives superior image quality. |
| Maximum gradient strength | 45 mT/m | Enables faster acquisitions while preserving high image quality. |
This hardware setup is widely used in clinical practice. It balances acquisition time, image quality, and patient comfort.
Before we can perform any MRI protocol, we must always capture initial localizer images of the patient. These images act as a guide for planning the detailed scans we will perform next.
We should always capture localizers in three planes:
Once acquired, load the initial localizer images into the three viewports.
Then, scroll through each of the image stacks to locate a central slice that clearly shows the anatomy of the brain.
✅ Correct Setup of Localizer Images for Routine Brain MRI:

When all preparations are ready, we can start planning and acquiring the protocol sequences.
Let’s go through the pulse sequences that a standard brain MRI protocol includes, why we perform them, and how to set them up.
We mainly use fast or turbo spin echo sequences for this study. These sequences give fast, high-quality images with strong contrast and relatively few artifacts, which makes them well suited to routine clinical imaging.
Turbo spin echo sequences also let us create several types of contrast, including T2, T1, and inversion recovery contrast, which is what allows FLAIR to null the signal from cerebrospinal fluid.
This helps us assess the brain's structure, detect abnormalities, and identify common pathologies like tumors, strokes, and demyelination.
In the sections below, we go through how to plan and set up each sequence.
✅ Correct Planning:

Planning Instructions:
Parameters for Axial T2 TSE:
| Parameter | Recommended Values | Why These Values |
|---|---|---|
| Echo Time (TE) | 100–130 ms | Longer TE is required for T2 contrast. |
| Repetition Time (TR) | 4,000–6,000 ms | Longer TR is required for T2 contrast. |
| Field-of-View (FOV) | 210 x 250 mm | Large enough to cover and fit the shape of the brain while avoiding wrap-around artifacts. |
| Matrix | 384 x 288 | ~0.55 × 0.87 mm in-plane, fine enough for cortical and periventricular detail. |
| Foldover Direction (Phase) | Anterior-to-Posterior (AP) | Aligned with the extended phase FOV; keeps any residual ghosting along AP. |
| Number of Slices | 20–23 | Enough slices to fully cover the brain region. |
| Slice Thickness | 6 mm | Medium thickness to get good resolution, without sacrificing scan time or SNR. |
| Slice Gap | 1 mm | Roughly 15–20% of slice thickness. Limits cross-talk without hiding anatomy. |
| NEX / Averages | 1–2 | To get enough SNR, while keeping scan time short. |
| Turbo Factor / ETL | 16–24 | Higher turbo factor reduces scan time, and long effective TE provides T2 weighting. |
| Bandwidth per pixel | 250–320 Hz/px | Moderate bandwidth balances chemical shift against SNR. |
| Fold-over Suppression | No | Not needed. The extended phase FOV already prevents wrap-around. |
✅ Correct Planning:

Planning Instructions:
Parameters for Axial T2 FLAIR:
| Parameter | Recommended Values | Why These Values |
|---|---|---|
| Echo Time (TE) | 100–140 ms | Produces T2 contrast under the inversion pulse. |
| Repetition Time (TR) | 8,000–10,000 ms | Lets CSF magnetization recover fully before the next inversion pulse, so the null holds. |
| Inversion Time (TI) | 1,800–2,500 ms | High enough TI to match the cerebrospinal fluid’s null point and suppress its signal at 1.5 T. |
| Field-of-View (FOV) | 210 x 250 mm | Large enough to cover and fit the shape of the brain while avoiding wrap-around artifacts. |
| Matrix | 384 x 288 | ~0.55 × 0.87 mm in-plane, fine enough for cortical and periventricular detail. |
| Foldover Direction (Phase) | Anterior-to-Posterior (AP) | Aligned with the extended phase FOV; keeps any residual ghosting along AP. |
| Number of Slices | 20–23 | Enough slices to fully cover the brain region. |
| Slice Thickness | 6 mm | Medium thickness to get good resolution, without sacrificing scan time or SNR. |
| Slice Gap | 1 mm | Roughly 15–20% of slice thickness. Limits cross-talk without hiding anatomy. |
| NEX / Averages | 1–2 | To get enough SNR, while keeping scan time short. |
| Turbo Factor / ETL | 16–24 | Higher turbo factor reduces scan time, and long effective TE provides T2 weighting. |
| Bandwidth per pixel | 250–320 Hz/px | Moderate bandwidth balances chemical shift against SNR. |
| Fold-over Suppression | No | Not needed. The extended phase FOV already prevents wrap-around. |
| Fat Suppression | Spectral | To suppress fat signal from orbital and scalp, which enhances lesion visibility. |
A note on averages in FLAIR:
FLAIR is the noisiest sequence in this protocol, because nulling the CSF signal also removes signal that would otherwise contribute to the image. Acquiring it with a single average keeps the scan short, but the result can be noticeably grainy, and fine structures such as the layers around the suppressed CSF spaces become hard to separate.
Going from one average to two doubles the acquisition time and improves SNR by roughly 40%. Which choice is right depends on the question being asked. If the noise level still answers the referral, one average is the better use of the slot. If subtle periventricular lesions are the point of the study, two averages is worth the extra time.
✅ Correct Planning:

Planning Instructions:
Parameters for Axial T1 TSE:
| Parameter | Recommended Values | Why These Values |
|---|---|---|
| Echo Time (TE) | 10–20 ms | Shorter TE is required for T1 contrast. |
| Repetition Time (TR) | 400–600 ms | Shorter TR is required for T1 contrast. |
| Field-of-View (FOV) | 210 x 250 mm | Large enough to cover and fit the shape of the brain while avoiding wrap-around artifacts. |
| Matrix | 384 x 288 | ~0.55 × 0.87 mm in-plane, fine enough for cortical and periventricular detail. |
| Foldover Direction (Phase) | Anterior-to-Posterior (AP) | Aligned with the extended phase FOV; keeps any residual ghosting along AP. |
| Number of Slices | 20–23 | Enough slices to fully cover the brain region. |
| Slice Thickness | 6 mm | Medium thickness to get good resolution, without sacrificing scan time or SNR. |
| Slice Gap | 1 mm | Roughly 15–20% of slice thickness. Limits cross-talk without hiding anatomy. |
| NEX / Averages | 1–2 | To get enough SNR, while keeping scan time short. |
| Turbo Factor / ETL | 2–4 | Kept short so the effective TE stays short, preserving T1-weighting. |
| Bandwidth per pixel | 250–320 Hz/px | Moderate bandwidth balances chemical shift against SNR. |
| Fold-over Suppression | No | Not needed. The extended phase FOV already prevents wrap-around. |
✅ Correct Planning:

Planning Instructions:
Parameters for Sagittal T1 TSE:
| Parameter | Recommended Values | Why These Values |
|---|---|---|
| Echo Time (TE) | 10–20 ms | Shorter TE is required for T1 contrast. |
| Repetition Time (TR) | 400–600 ms | Shorter TR is required for T1 contrast. |
| Field-of-View (FOV) | 220 x 240 mm | Large enough to cover the brain while avoiding wrap-around artifacts. |
| Matrix | 320 x 224 | ~0.69 × 1.07 mm in-plane. Coarser than the axials since this series is for midline orientation, not lesion detection |
| Foldover Direction (Phase) | Anterior-to-Posterior (AP) | Keeps neck and shoulder signal from folding into the brain. |
| Number of Slices | 20–23 | Enough slices to fully cover the brain region. |
| Slice Thickness | 6 mm | Medium thickness to get good resolution, without sacrificing scan time or SNR. |
| Slice Gap | 1 mm | Roughly 15–20% of slice thickness. Limits cross-talk without hiding anatomy. |
| NEX / Averages | 1–2 | To get enough SNR, while keeping scan time short. |
| Turbo Factor / ETL | 2–4 | Kept short so the effective TE stays short, preserving T1-weighting. |
| Bandwidth per pixel | 250–320 Hz/px | Moderate bandwidth balances chemical shift against SNR. |
| Fold-over Suppression | No | Not needed. The extended phase FOV already prevents wrap-around. |
✅ Correct Planning:

Planning Instructions:
Parameters for Coronal T1 TSE:
| Parameter | Recommended Values | Why These Values |
|---|---|---|
| Echo Time (TE) | 10–20 ms | Shorter TE is required for T1 contrast. |
| Repetition Time (TR) | 400–600 ms | Shorter TR is required for T1 contrast. |
| Field-of-View (FOV) | 220 x 200 mm | Large enough to cover the brain while avoiding wrap-around artifacts. |
| Matrix | 320 x 224 | ~0.69 × 0.89 mm in-plane, enough for temporal lobe and hippocampal detail. |
| Foldover Direction (Phase) | Right-to-Left (RL) | To keep field-of-view small and minimize left-right wrap-around artifacts. |
| Number of Slices | 23–26 | Enough slices to fully cover the brain region. |
| Slice Thickness | 6 mm | Medium thickness to get good resolution, without sacrificing scan time or SNR. |
| Slice Gap | 1 mm | Roughly 15–20% of slice thickness. Limits cross-talk without hiding anatomy. |
| NEX / Averages | 1–2 | To get enough SNR, while keeping scan time short. |
| Turbo Factor / ETL | 2–4 | Kept short so the effective TE stays short, preserving T1-weighting. |
| Bandwidth per pixel | 250–320 Hz/px | Moderate bandwidth balances chemical shift against SNR. |
| Fold-over Suppression | No | Not needed. The extended phase FOV already prevents wrap-around. |
✅ Correct Planning:

Planning Instructions:
Parameters for Axial DWI:
| Parameter | Recommended Values | Why These Values |
|---|---|---|
| Echo Time (TE) | 70–100 ms | Set by the diffusion gradient pair, not chosen directly for contrast. |
| Repetition Time (TR) | 4,000–6,000 ms | Removes T1 influence and fits all slices into one TR. |
| Field-of-View (FOV) | 210 x 250 mm | Large enough to cover and fit the shape of the brain while avoiding wrap-around artifacts. |
| Matrix | 64 x 100 | ~3.3 × 2.5 mm in-plane. Kept coarse to shorten the echo train and limit distortion, but fine enough not to lose a small infarct. |
| Foldover Direction (Phase) | Anterior-to-Posterior (AP) | To contain geometric distortions to the AP direction rather than the left-right axis, where distortion would be harder to read around. |
| Number of Slices | 14–18 | To cover key brain regions while minimizing susceptibility artifacts from air-filled sinuses and mouth areas. |
| Slice Thickness | 6 mm | Medium thickness to get good resolution, without sacrificing scan time or SNR. |
| Slice Gap | 1 mm | Roughly 15–20% of slice thickness. Limits cross-talk without hiding anatomy. |
| NEX / Averages | 2–4 | EPI at b=1000 is signal-starved; extra averages are cheap here. |
| Turbo Factor / ETL | N/A | DWI uses echo-planar imaging instead of turbo/fast spin echo acquisition methods. |
| Bandwidth per pixel | 600–800 Hz/px | Shortens EPI echo spacing, limiting distortion and minimum TE. |
| Fold-over Suppression | No | Not needed. The extended phase FOV already prevents wrap-around. |
| B-value | 0 and 1,000 s/mm² | The standard routine brain pair. b=0 gives the unweighted reference, b=1000 gives strong sensitivity to restricted diffusion without excessive signal loss in normal tissue. Some protocols add an intermediate value such as 500 s/mm² for specialised assessments. |
| Scan mode | 3-scan trace | Combines three gradient directions so no lesion is missed on an unmeasured axis. |
| Output Trace DWI | Yes | Produces the trace image that acute infarcts appear bright on. |
| Output ADC | Yes | Produces the ADC map, which separates true restricted diffusion from T2 shine-through. |
The table below lists the 6 common brain artifacts, and what techniques you can use to avoid them:
| Artifacts | Solution – How to Avoid It |
|---|---|
| Motion artifacts | Shorten the scan time to reduce the risk of patient movement. |
| Susceptibility artifacts | Use spin echo instead of gradient echo sequences to reduce sensitivity to magnetic field inhomogeneities. |
| Chemical shift artifacts | Increase the bandwidth to reduce the spatial displacement between fat and water signals. |
| CSF flow artifacts | Use flow compensation gradients to correct CSF-related phase shifts. FLAIR also reduces this artifact by nulling the CSF signal itself. |
| Truncation artifacts | Increase the resolution to capture more frequency information and reduce Gibbs ringing at tissue boundaries. |
| Wrap-around artifacts | Activate fold-over suppression to prevent anatomy outside the field of view from overlapping. |
Finally, we will review the images to ensure all the anatomical information we need is clear.
These key structures must be clearly visible in a brain MRI:
Below, we will go through all the different image contrasts and explain their specific role in imaging the brain.
T2-weighted imaging makes fluids appear bright. This contrast is ideal for detecting tissues and abnormalities associated with high water content.
In brain MRI, T2 sequences are excellent for evaluating hydrocephalus, cysts, and edema. They clearly show the ventricles and cerebrospinal fluid spaces, making them useful for assessing size and configuration of these structures.
✅ Axial T2 of the Brain – Correct Image:

The axial T2 sequence provides a horizontal view of the brain, which lets us:
T2 FLAIR (Fluid Attenuated Inversion Recovery) is a special type of T2-weighted sequence that suppresses the signal from cerebrospinal fluid (CSF), making it appear dark instead of bright. This contrast is ideal for detecting lesions adjacent to CSF spaces.
In brain MRI, FLAIR sequences are important for evaluating multiple sclerosis, small vessel disease, and chronic ischemia. They are particularly effective at highlighting white matter lesions near the ventricles.
✅ Axial T2 FLAIR of the Brain – Correct Image:

The axial T2 FLAIR sequence provides a view similar to T2, but with CSF suppression, which lets us:
T1-weighted imaging makes fat appear bright and fluid dark. This contrast is ideal for fat-rich tissues and structural abnormalities.
In brain MRI, T1 sequences are used to evaluate structural anatomy, tumors, metastases, and subacute hemorrhage. They provide excellent contrast between gray and white matter, and serve as the baseline for post-contrast studies.
✅ Axial T1 of the Brain – Correct Image:

The axial T1 sequence provides a horizontal view, showing:
✅ Sagittal T1 of the Brain – Correct Image:

The sagittal T1 sequence provides a side view of the brain, which lets us:
✅ Coronal T1 of the Brain – Correct Image:

The coronal T1 sequence provides a front-to-back view, useful for:
Diffusion-weighted imaging is sensitive to the movement of water molecules in tissue. In normal brain tissue, water diffuses freely, but in damaged areas (like in acute stroke), water movement is restricted.
In brain MRI, DWI is the key technique for evaluating acute stroke and cytotoxic edema. It can detect ischemic changes within minutes of onset, making invaluable for early stroke diagnosis.
The DWI sequence generates 3 different types of images from a single acquisition, each providing unique diagnostic information:
The b=0 image is acquired at the start of the diffusion sequence with no diffusion gradients applied. It is effectively a T2-weighted EPI image showing baseline tissue contrast before any diffusion weighting.
It serves two purposes:
Because it is an EPI readout with no diffusion gradients, this is also the image where susceptibility effects near air-tissue interfaces and metal are easiest to spot. Some departments therefore call it the susceptibility image informally.
It is not a susceptibility map, and on its own it cannot be used to correct geometric distortion, which needs either a field map or a second acquisition with reversed phase-encode polarity.
✅ Correct Image Example:

The True Diffusion Image (b=1000) shows areas of restricted water diffusion as bright signal intensity. It detects acute ischemic changes where water movement is restricted due to cytotoxic edema.
This is the primary image for identifying acute stroke, showing the infarct core as a hyperintense (bright) region within minutes of symptom onset.
✅ Correct Image Example:

The ADC (Apparent Diffusion Coefficient) Map quantifies the degree of water diffusion, where restricted diffusion appears dark.
The map verifies whether bright areas on the DWI are truly due to restricted water movement (as in acute stroke), or simply because the tissue naturally appears bright on T2-weighted images (called "T2 shine-through"). This distinction decides the diagnosis.
The map also separates acute ischemia from subacute and chronic lesions. Acute stroke appears dark on ADC maps, while chronic lesions typically show normal or increased diffusion.
✅ Correct Image Example:

When these three DWI images are evaluated together, they provide comprehensive information about water diffusion in brain tissue.
This enables accurate diagnosis of acute ischemia, and lets us differentiate it from other pathologies that appear similar on standard sequences.
Before finishing a brain MRI, always check these 6 points to ensure diagnostic quality:
By following this protocol and carefully reviewing the images, you can ensure an excellent diagnostic evaluation of the brain.