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Track-weighted imaging methods: extracting information from a streamlines tractogram

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Abstract

A whole-brain streamlines data-set (so-called tractogram) generated from diffusion MRI provides a wealth of information regarding structural connectivity in the brain. Besides visualisation strategies, a number of post-processing approaches have been proposed to extract more detailed information from the tractogram. One such approach is based on exploiting the information contained in the tractogram to generate track-weighted (TW) images. In the track-weighted imaging (TWI) approach, a very large number of streamlines are often generated throughout the brain, and an image is then computed based on properties of the streamlines themselves (e.g. based on the number of streamlines in each voxel, or their average length), or based on the values of an associated image (e.g. a diffusion anisotropy map, a T2 map) measured at the coordinates of the streamlines. This review article describes various approaches used to generate TW images and discusses the flexible formalism that TWI provides to generate a range of images with very different contrast, as well as the super-resolution properties of the resulting images. It also explains how this approach provides a powerful means to study structural and functional connectivity simultaneously. Finally, a number of key issues for its practical implementation are discussed.

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Notes

  1. Throughout this work, the terms “streamline” and “track” are used interchangeably, to represent a mathematical representation (i.e. a three-dimensional curve generated using a tractography algorithm). In contrast, the terms “tract” and “white matter pathway” are also used interchangeably to represent the actual biological structure in the brain.

  2. The TOI is equivalent to the commonly used region of interest (ROI), for the particular case that its extent is determined by the volume occupied by a set of streamlines (typically corresponding to a given white matter structure).

  3. ACM and FDM are essentially similar to TDI at native resolution (i.e. without applying super-resolution).

  4. In the TDI analogy as a histogram map, super-resolution can be seen as the fact that the bin size (i.e. voxel size) can be, to some extent, arbitrarily chosen.

  5. The term “fixel” was introduced in that paper to refer to a specific fibre population within a single voxel.

References

  1. Tournier J-D, Mori S, Leemans A (2011) Diffusion tensor imaging and beyond. Magn Reson Med 65:1532–1556

    Article  PubMed  PubMed Central  Google Scholar 

  2. Mori S, Crain BJ, Chacko VP, van Zijl PC (1999) Three-dimensional tracking of axonal projections in the brain by magnetic resonance imaging. Ann Neurol 45:265–269

    Article  CAS  PubMed  Google Scholar 

  3. Conturo TE, Lori NF, Cull TS, Akbudak E, Snyder AZ, Shimony JS, McKinstry RC, Burton H, Raichle ME (1999) Tracking neuronal fiber pathways in the living human brain. Proc Natl Acad Sci USA 96:10422–10427

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  4. Tournier J-D, Calamante F, Connelly A (2012) MRtrix: diffusion tractography in crossing fiber regions. Int J Imaging Syst Technol 22:53–66

    Article  Google Scholar 

  5. Behrens TEJ, Johansen-Berg H, Woolrich MW, Smith SM, Wheeler-Kingshott CAM, Boulby PA, Barker GJ, Sillery EL, Sheehan K, Ciccarelli O, Thompson AJ, Brady JM, Matthews PM (2003) Non-invasive mapping of connections between human thalamus and cortex using diffusion imaging. Nat Neurosci 6:750–757

    Article  CAS  PubMed  Google Scholar 

  6. Hagmann P, Kurant M, Gigandet X, Thiran P, Wedeen VJ, Meuli R, Thiran J-P (2007) Mapping human whole-brain structural networks with diffusion MRI. PLoS One 2:e597

    Article  PubMed  PubMed Central  Google Scholar 

  7. Fornito A, Zalesky A, Breakspear M (2013) Graph analysis of the human connectome: promise, progress, and pitfalls. Neuroimage 80:426–444

    Article  PubMed  Google Scholar 

  8. Fornito A, Zalesky A, Breakspear M (2015) The connectomics of brain disorders. Nat Rev Neurosci 16:159–172

    Article  CAS  PubMed  Google Scholar 

  9. Correia S, Lee SY, Voorn T, Tate DF, Paul RH, Zhang S, Salloway SP, Malloy PF, Laidlaw DH (2008) Quantitative tractography metrics of white matter integrity in diffusion-tensor MRI. Neuroimage 42:568–581

    Article  PubMed  PubMed Central  Google Scholar 

  10. Berman JI, Mukherjee P, Partridge SC, Miller SP, Ferriero DM, Barkovich AJ, Vigneron DB, Henry RG (2005) Quantitative diffusion tensor MRI fiber tractography of sensorimotor white matter development in premature infants. Neuroimage 27:862–871

    Article  PubMed  Google Scholar 

  11. Jones DK, Travis AR, Eden G, Pierpaoli C, Basser PJ (2005) PASTA: pointwise assessment of streamline tractography attributes. Magn Reson Med 53:1462–1467

    Article  PubMed  Google Scholar 

  12. Yeatman JD, Dougherty RF, Myall NJ, Wandell BA, Feldman HM (2012) Tract profiles of white matter properties: automating fiber-tract quantification. PLoS One 7:e49790

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  13. Colby JB, Soderberg L, Lebel C, Dinov ID, Thompson PM, Sowell ER (2012) Along-tract statistics allow for enhanced tractography analysis. Neuroimage 59:3227–3242

    Article  PubMed  Google Scholar 

  14. Mezer A, Yeatman JD, Stikov N, Kay KN, Cho N-J, Dougherty RF, Perry ML, Parvizi J, Hua LH, Butts-Pauly K, Wandell BA (2013) Quantifying the local tissue volume and composition in individual brains with magnetic resonance imaging. Nat Med 19:1667–1672

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  15. Travis KE, Golden NH, Feldman HM, Solomon M, Nguyen J, Mezer A, Yeatman JD, Dougherty RF (2015) Abnormal white matter properties in adolescent girls with anorexia nervosa. Neuroimage Clin 9:648–659

    Article  PubMed  PubMed Central  Google Scholar 

  16. Batchelor PG, Calamante F, Tournier J-D, Atkinson D, Hill DLG, Connelly A (2006) Quantification of the shape of fiber tracts. Magn Reson Med 55:894–903

    Article  CAS  PubMed  Google Scholar 

  17. Calamante F, Tournier J-D, Smith RE, Connelly A (2012) A generalised framework for super-resolution track-weighted imaging. Neuroimage 59:2494–2503

    Article  PubMed  Google Scholar 

  18. Embleton K, Morris D, Haroon H, Lambon Ralph M (2007) Anatomica Connectivity Mapping. Proceedings of the International Society for Magnetic Resonance in Medicine (ISMRM), 15th Annual Meeting, Berlin, Germany, (pp 19–25 May 1548)

  19. Calamante F, Tournier J-D, Jackson GD, Connelly A (2010) Track-density imaging (TDI): super-resolution white matter imaging using whole-brain track-density mapping. Neuroimage 53:1233–1243

    Article  PubMed  Google Scholar 

  20. Bozzali M, Parker GJM, Serra L, Embleton K, Gili T, Perri R, Caltagirone C, Cercignani M (2011) Anatomical connectivity mapping: a new tool to assess brain disconnection in Alzheimer’s disease. Neuroimage 54:2045–2051

    Article  PubMed  Google Scholar 

  21. Stadlbauer A, Buchfelder M, Salomonowitz E, Ganslandt O (2010) Fiber density mapping of gliomas: histopathologic evaluation of a diffusion-tensor imaging data processing method. Radiology 257:846–853

    Article  PubMed  Google Scholar 

  22. Pannek K, Mathias JL, Bigler ED, Brown G, Taylor JD, Rose SE (2011) The average pathlength map: a diffusion MRI tractography-derived index for studying brain pathology. Neuroimage 55:133–141

    Article  PubMed  Google Scholar 

  23. Calamante F, Tournier J-D, Heidemann RM, Anwander A, Jackson GD, Connelly A (2011) Track density imaging (TDI): validation of super resolution property. Neuroimage 56:1259–1266

    Article  PubMed  Google Scholar 

  24. Calamante F, Tournier J-D, Kurniawan ND, Yang Z, Gyengesi E, Galloway GJ, Reutens DC, Connelly A (2012) Super-resolution track-density imaging studies of mouse brain: comparison to histology. Neuroimage 59:286–296

    Article  PubMed  Google Scholar 

  25. Pajevic S, Pierpaoli C (2000) Color schemes to represent the orientation of anisotropic tissues from diffusion tensor data: application to white matter fiber tract mapping in the human brain. Magn Reson Med 43:921

    Article  CAS  PubMed  Google Scholar 

  26. Dhollander T, Smith R, Tournier J-D, Jeurissen B, Connelly A (2015) Time to move on: an FOD-based DEC map to replace DTI’s trademark DEC FA. Proceedings of International Society for Magnetic Resonance in Medicine (ISMRM), 23rd Annual Meeting, Toronto, Canada 1027

  27. Calamante F, Oh S-H, Tournier J-D, Park S-Y, Son Y-D, Chung J-Y, Chi J-G, Jackson GD, Park C-W, Kim Y-B, Connelly A, Cho Z-H (2013) Super-resolution track-density imaging of thalamic substructures: comparison with high-resolution anatomical magnetic resonance imaging at 7.0T. Hum Brain Mapp 34:2538–2548

    Article  PubMed  Google Scholar 

  28. Cho ZH, Calamante F, Chi JG (2015) 7.0 Tesla MRI brain white matter atlas, 2nd edn. Springer, New York

    Google Scholar 

  29. Hoch MJ, Chung S, Ben-Eliezer N, Bruno MT, Fatterpekar GM, Shepherd TM (2016) New clinically feasible 3T MRI protocol to discriminate internal brain stem anatomy. Am J Neuroradiol 37:1058–1065

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  30. Wenz H, Al-Zghloul M, Hart E, Kurth S, Groden C, Förster A (2016) Track-density imaging of the human brainstem for anatomic localization of fiber tracts and nerve nuclei in Vivo: initial experience with 3-T magnetic resonance imaging. World Neurosurg 93:286–292

    Article  PubMed  Google Scholar 

  31. Palesi F, Tournier J-D, Calamante F, Muhlert N, Castellazzi G, Chard D, D’Angelo E, Wheeler-Kingshott CAM (2015) Contralateral cerebello-thalamo-cortical pathways with prominent involvement of associative areas in humans in vivo. Brain Struct Funct 220:3369–3384

    Article  PubMed  Google Scholar 

  32. Kurniawan ND, Richards KL, Yang Z, She D, Ullmann JFP, Moldrich RX, Liu S, Yaksic JU, Leanage G, Kharatishvili I, Wimmer V, Calamante F, Galloway GJ, Petrou S, Reutens DC (2014) Visualization of mouse barrel cortex using ex vivo track density imaging. Neuroimage 87:465–475

    Article  PubMed  Google Scholar 

  33. Richards K, Calamante F, Tournier J-D, Kurniawan ND, Sadeghian F, Retchford AR, Jones GD, Reid CA, Reutens DC, Ordidge R, Connelly A, Petrou S (2014) Mapping somatosensory connectivity in adult mice using diffusion MRI tractography and super-resolution track density imaging. Neuroimage 102(Pt 2):381–392

    Article  PubMed  Google Scholar 

  34. Ullmann JFP, Calamante F, Collin SP, Reutens DC, Kurniawan ND (2015) Enhanced characterization of the zebrafish brain as revealed by super-resolution track-density imaging. Brain Struct Funct 220:457–468

    Article  CAS  PubMed  Google Scholar 

  35. Hamaide J, De Groof G, Van Steenkiste G, Jeurissen B, Van Audekerke J, Naeyaert M, Van Ruijssevelt L, Cornil C, Sijbers J, Verhoye M, Van der Linden A (2016) Exploring sex differences in the adult zebra finch brain: in vivo diffusion tensor imaging and ex vivo super-resolution track density imaging. Neuroimage. doi:10.1016/j.neuroimage.2016.09.067

    Google Scholar 

  36. Tournier J-D, Calamante F, Connelly A (2007) Robust determination of the fibre orientation distribution in diffusion MRI: non-negativity constrained super-resolved spherical deconvolution. Neuroimage 35:1459–1472

    Article  PubMed  Google Scholar 

  37. Farquharson S, Tournier J-D, Calamante F, Fabinyi G, Schneider-Kolsky M, Jackson GD, Connelly A (2013) White matter fiber tractography: why we need to move beyond DTI. J Neurosurg 118:1367–1377

    Article  PubMed  Google Scholar 

  38. Smith RE, Tournier J-D, Calamante F, Connelly A (2012) Anatomically-constrained tractography: improved diffusion MRI streamlines tractography through effective use of anatomical information. Neuroimage 62:1924–1938

    Article  PubMed  Google Scholar 

  39. Smith RE, Tournier J-D, Calamante F, Connelly A (2013) SIFT: spherical-deconvolution informed filtering of tractograms. Neuroimage 67:298–312

    Article  PubMed  Google Scholar 

  40. Reisert M, Mader I, Anastasopoulos C, Weigel M, Schnell S, Kiselev V (2011) Global fiber reconstruction becomes practical. Neuroimage 54:955–962

    Article  PubMed  Google Scholar 

  41. Daducci A, Dal Palú A, Descoteaux M, Thiran J-P (2016) Microstructure Informed Tractography: pitfalls and open challenges. Front Neurosci 10:247

    Article  PubMed  PubMed Central  Google Scholar 

  42. Sotiropoulos SN, Jbabdi S, Xu J, Andersson JL, Moeller S, Auerbach EJ, Glasser MF, Hernandez M, Sapiro G, Jenkinson M, Feinberg DA, Yacoub E, Lenglet C, Van Essen DC, Ugurbil K, Behrens TEJ, WU-Minn HCP Consortium (2013) Advances in diffusion MRI acquisition and processing in the human connectome project. Neuroimage 80:125–143

    Article  PubMed  PubMed Central  Google Scholar 

  43. McNab JA, Edlow BL, Witzel T, Huang SY, Bhat H, Heberlein K, Feiweier T, Liu K, Keil B, Cohen-Adad J, Tisdall MD, Folkerth RD, Kinney HC, Wald LL (2013) The Human Connectome Project and beyond: initial applications of 300 mT/m gradients. Neuroimage 80:234–245

    Article  PubMed  Google Scholar 

  44. Jeurissen B, Tournier J-D, Dhollander T, Connelly A, Sijbers J (2014) Multi-tissue constrained spherical deconvolution for improved analysis of multi-shell diffusion MRI data. Neuroimage 103:411–426

    Article  PubMed  Google Scholar 

  45. Smith RE, Tournier J-D, Calamante F, Connelly A (2015) SIFT2: enabling dense quantitative assessment of brain white matter connectivity using streamlines tractography. Neuroimage 119:338–351

    Article  PubMed  Google Scholar 

  46. Smith RE, Tournier J-D, Calamante F, Connelly A (2015) The effects of SIFT on the reproducibility and biological accuracy of the structural connectome. Neuroimage 104:253–265

    Article  PubMed  Google Scholar 

  47. Daducci A, Dal Palù A, Lemkaddem A, Thiran J-P (2015) COMMIT: convex optimization modeling for microstructure informed tractography. IEEE Trans Med Imaging 34:246–257

    Article  PubMed  Google Scholar 

  48. Girard G, Whittingstall K, Deriche R, Descoteaux M (2014) Towards quantitative connectivity analysis: reducing tractography biases. Neuroimage 98:266–278

    Article  PubMed  Google Scholar 

  49. Jones DK (2010) Challenges and limitations of quantifying brain connectivity in vivo with diffusion MRI. Imaging Med 2:341–355

    Article  Google Scholar 

  50. Li L, Rilling JK, Preuss TM, Glasser MF, Hu X (2012) The effects of connection reconstruction method on the interregional connectivity of brain networks via diffusion tractography. Hum Brain Mapp 33:1894–1913

    Article  PubMed  Google Scholar 

  51. Barajas RF, Hess CP, Phillips JJ, Von Morze CJ, Yu JP, Chang SM, Nelson SJ, McDermott MW, Berger MS, Cha S (2013) Super-resolution track density imaging of glioblastoma: histopathologic correlation. Am J Neuroradiol 34:1319–1325

    Article  PubMed  PubMed Central  Google Scholar 

  52. Stadlbauer A, Hammen T, Grummich P, Buchfelder M, Kuwert T, Dörfler A, Nimsky C, Ganslandt O (2011) Classification of peritumoral fiber tract alterations in gliomas using metabolic and structural neuroimaging. J Nucl Med 52:1227–1234

    Article  PubMed  Google Scholar 

  53. Ziegler E, Rouillard M, André E, Coolen T, Stender J, Balteau E, Phillips C, Garraux G (2014) Mapping track density changes in nigrostriatal and extranigral pathways in Parkinson’s disease. Neuroimage 99:498–508

    Article  PubMed  PubMed Central  Google Scholar 

  54. Bozzali M, Parker GJM, Spanò B, Serra L, Giulietti G, Perri R, Magnani G, Marra C, Vita GM, Caltagirone C, Cercignani M (2013) Brain tissue modifications induced by cholinergic therapy in Alzheimer’s disease. Hum Brain Mapp 34:3158–3167

    Article  PubMed  Google Scholar 

  55. Bozzali M, Spanò B, Parker GJM, Giulietti G, Castelli M, Basile B, Rossi S, Serra L, Magnani G, Nocentini U, Caltagirone C, Centonze D, Cercignani M (2013) Anatomical brain connectivity can assess cognitive dysfunction in multiple sclerosis. Mult Scler 19:1161–1168

    Article  CAS  PubMed  Google Scholar 

  56. Lyksborg M, Siebner HR, Sørensen PS, Blinkenberg M, Parker GJM, Dogonowski A-M, Garde E, Larsen R, Dyrby TB (2014) Secondary progressive and relapsing remitting multiple sclerosis leads to motor-related decreased anatomical connectivity. PLoS One 9:e95540

    Article  PubMed  PubMed Central  Google Scholar 

  57. Tan XL, Wright DK, Liu S, Hovens C, O’Brien TJ, Shultz SR (2016) Sodium selenate, a protein phosphatase 2A activator, mitigates hyperphosphorylated tau and improves repeated mild traumatic brain injury outcomes. Neuropharmacology 108:382–393

    Article  CAS  PubMed  Google Scholar 

  58. Vaessen MJ, Saj A, Lovblad K-O, Gschwind M, Vuilleumier P (2016) Structural white-matter connections mediating distinct behavioral components of spatial neglect in right brain-damaged patients. Cortex 77:54–68

    Article  PubMed  Google Scholar 

  59. Stadlbauer A, Ganslandt O, Salomonowitz E, Buchfelder M, Hammen T, Bachmair J, Eberhardt K (2012) Magnetic resonance fiber density mapping of age-related white matter changes. Eur J Radiol 81:4005–4012

    Article  PubMed  Google Scholar 

  60. Woodworth D, Mayer E, Leu K, Ashe-McNalley C, Naliboff BD, Labus JS, Tillisch K, Kutch JJ, Farmer MA, Apkarian AV, Johnson KA, Mackey SC, Ness TJ, Landis JR, Deutsch G, Harris RE, Clauw DJ, Mullins C, Ellingson BM, MAPP Research Network (2015) Unique Mmicrostructural changes in the brain associated with urological chronic pelvic pain syndrome (UCPPS) revealed by diffusion tensor MRI, super-resolution track density imaging, and statistical parameter mapping: a MAPP network neuroimaging study. PLoS One 10:e0140250

    Article  PubMed  PubMed Central  Google Scholar 

  61. Ellingson BM, Salamon N, Woodworth DC, Holly LT (2015) Correlation between degree of subvoxel spinal cord compression measured with super-resolution tract density imaging and neurological impairment in cervical spondylotic myelopathy. J Neurosurg Spine 22:631–638

    Article  PubMed  Google Scholar 

  62. Willats L, Raffelt D, Smith RE, Tournier J-D, Connelly A, Calamante F (2013) Quantification of track-weighted imaging (TWI): characterisation of within-subject reproducibility and between-subject variability. Neuroimage 87:18–31

    Article  PubMed  Google Scholar 

  63. Calamante F, Smith RE, Tournier J-D, Raffelt D, Connelly A (2015) Quantification of voxel-wise total fibre density: investigating the problems associated with track-count mapping. Neuroimage 117:284–293

    Article  PubMed  Google Scholar 

  64. Calamante F (2016) Super-resolution track density imaging: anatomic detail versus quantification. Am J Neuroradiol 37:1066–1067

    Article  CAS  PubMed  Google Scholar 

  65. Besseling RMH, Jansen JFA, Overvliet GM, Vaessen MJ, Braakman HMH, Hofman PAM, Aldenkamp AP, Backes WH (2012) Tract specific reproducibility of tractography based morphology and diffusion metrics. PLoS One 7:e34125

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  66. Bloy L, Ingalhalikar M, Batmanghelich NK, Schultz RT, Roberts TPL, Verma R (2012) An integrated framework for high angular resolution diffusion imaging-based investigation of structural connectivity. Brain Connect 2:69–79

    Article  PubMed  PubMed Central  Google Scholar 

  67. Pannek K, Mathias JL, Rose SE (2011) MRI diffusion indices sampled along streamline trajectories: quantitative tractography mapping. Brain Connect 1:331–338

    Article  PubMed  Google Scholar 

  68. Jones DK, Knösche TR, Turner R (2013) White matter integrity, fiber count, and other fallacies: the do’s and don’ts of diffusion MRI. Neuroimage 73:239–254

    Article  PubMed  Google Scholar 

  69. Raffelt D, Tournier J-D, Rose S, Ridgway GR, Henderson R, Crozier S, Salvado O, Connelly A (2012) Apparent Fibre Density: a novel measure for the analysis of diffusion-weighted magnetic resonance images. Neuroimage 59:3976–3994

    Article  PubMed  Google Scholar 

  70. Dell’Acqua F, Simmons A, Williams SCR, Catani M (2013) Can spherical deconvolution provide more information than fiber orientations? Hindrance modulated orientational anisotropy, a true-tract specific index to characterize white matter diffusion. Hum Brain Mapp 34:2464–2483

    Article  PubMed  Google Scholar 

  71. Raffelt DA, Smith RE, Ridgway GR, Tournier J-D, Vaughan DN, Rose S, Henderson R, Connelly A (2015) Connectivity-based fixel enhancement: whole-brain statistical analysis of diffusion MRI measures in the presence of crossing fibres. Neuroimage 117:40–55

    Article  PubMed  PubMed Central  Google Scholar 

  72. Pannek K, Raffelt D, Salvado O, Rose S (2012) Incorporating directional information in diffusion tractography derived maps: angular track imaging (ATI). Proceedings of the International Society for Magnetic Resonance in Medicine (ISMRM), 20th Annual Meeting, Toronto, Canada, vol 1912, pp 5–11

  73. Dhollander T, Emsell L, Van Hecke W, Maes F, Sunaert S, Suetens P (2014) Track orientation density imaging (TODI) and track orientation distribution (TOD) based tractography. Neuroimage 94:312–336

    Article  PubMed  Google Scholar 

  74. Bell C, Pannek K, Fay M, Thomas P, Bourgeat P, Salvado O, Gal Y, Coulthard A, Crozier S, Rose S (2014) Distance informed track-weighted imaging (diTWI): a framework for sensitising streamline information to neuropathology. Neuroimage 86:60–66

    Article  PubMed  Google Scholar 

  75. Irfanoglu MO, Walker L, Sarlls J, Marenco S, Pierpaoli C (2012) Effects of image distortions originating from susceptibility variations and concomitant fields on diffusion MRI tractography results. Neuroimage 61:275–288

    Article  PubMed  Google Scholar 

  76. Calamante F, Son Y-D, Tournier J-D, Ryu T-H, Oh S-H, Connelly A, Cho Z-H (2012) Fusing PET and MRI Data Using super-resolution track-weighted imaging. Proceedings of the International Society for Magnetic Resonance in Medicine (ISMRM), 20th Annual Meeting, Toronto, Canada, vol 1919, pp 5–11

  77. Smith S (2013) Introduction to the NeuroImage special issue “Mapping the Connectome”. Neuroimage 80:1

    Article  PubMed  Google Scholar 

  78. Calamante F, Masterton RAJ, Tournier J-D, Smith RE, Willats L, Raffelt D, Connelly A (2013) Track-weighted functional connectivity (TW-FC): a tool for characterizing the structural–functional connections in the brain. Neuroimage 70:199–210

    Article  PubMed  Google Scholar 

  79. Hutchison RM, Womelsdorf T, Allen EA, Bandettini PA, Calhoun VD, Corbetta M, Della Penna S, Duyn JH, Glover GH, Gonzalez-Castillo J, Handwerker DA, Keilholz S, Kiviniemi V, Leopold DA, de Pasquale F, Sporns O, Walter M, Chang C (2013) Dynamic functional connectivity: promise, issues, and interpretations. Neuroimage 80:360–378

    Article  PubMed  Google Scholar 

  80. Calamante F, Smith RE, Liang X, Zalesky A, Connelly A (2016) Track-weighted dynamic functional connectivity (TW-dFC): a new method to study dynamic connectivity. In: Proceedings of the international society for magnetic resonance in medicine (ISMRM), 24th Annual Meeting, Singapore, vol 308, pp 7–13

  81. Mori S, van Zijl PCM (2002) Fiber tracking: principles and strategies—a technical review. NMR Biomed 15:468–480

    Article  PubMed  Google Scholar 

  82. Lazar M, Alexander AL (2003) An error analysis of white matter tractography methods: synthetic diffusion tensor field simulations. Neuroimage 20:1140–1153

    Article  PubMed  Google Scholar 

  83. Tournier J-D, Calamante F, King MD, Gadian DG, Connelly A (2002) Limitations and requirements of diffusion tensor fiber tracking: an assessment using simulations. Magn Reson Med 47:701–708

    Article  PubMed  Google Scholar 

  84. Basser PJ, Pajevic S, Pierpaoli C, Duda J, Aldroubi A (2000) In vivo fiber tractography using DT-MRI data. Magn Reson Med 44:625–632

    Article  CAS  PubMed  Google Scholar 

  85. Ashburner J, Friston KJ (2000) Voxel-based morphometry—the methods. Neuroimage 11:805–821

    Article  CAS  PubMed  Google Scholar 

  86. Nichols TE, Holmes AP (2002) Nonparametric permutation tests for functional neuroimaging: a primer with examples. Hum Brain Mapp 15:1–25

    Article  PubMed  Google Scholar 

  87. Hayasaka S, Nichols TE (2004) Combining voxel intensity and cluster extent with permutation test framework. Neuroimage 23:54–63

    Article  PubMed  Google Scholar 

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Acknowledgements

We are grateful to the many colleagues and collaborators involved in the track-weighted imaging work, and in particular to Alan Connelly, Jacques-Donald Tournier, and Robert E. Smith for their extensive contribution to developing these methods. We are also grateful to Chun-Hung Yeh and Donna Parker for help in producing figures for this work. We thank the National Health and Medical Research Council (NHMRC) of Australia, the Australian Research Council (ARC), and the Victorian Government’s Operational Infrastructure Support Grant for their support.

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Correspondence to Fernando Calamante.

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FC is co-inventor in a patent application on the TDI method.

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This study was funded by the National Health and Medical Research Council (NHMRC) of Australia, the Australian Research Council (ARC), and the Victorian Government’s Operational Infrastructure Support Grant.

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Calamante, F. Track-weighted imaging methods: extracting information from a streamlines tractogram. Magn Reson Mater Phy 30, 317–335 (2017). https://doi.org/10.1007/s10334-017-0608-1

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