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The role of hippocampal subregions in detecting spatial novelty
Abstract
Previous literature suggests that the hippocampus subserves processes associated with the encoding of novel information. To investigate the role of different subregions of the hippocampus, the authors made neurotoxic lesions in different subregions of the dorsal hippocampus (i.e., CA1, dentate gyrus [DG], or CA3) of rats, followed by tests using a spontaneous object exploration paradigm. All lesion groups explored normally an object newly introduced in a familiar location. However, when some of the familiar objects were moved to novel locations, both DG and CA3 lesion groups were severely impaired in reexploring the displaced objects, whereas the CA1 lesion group was only mildly impaired in reexploration. The results suggest that the DG-CA3 network is essential in detecting novelty for spatial, but not for individual object, information.
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“Rodents showed preference for exploring the displaced object more than the stationary ones, indicating intact spatial recognition.”
From The medial prefrontal cortex - hippocampus circuit that integrates information of object, place and time to construct episodic memory in rodents: Behavioral, anatomical and neurochemical properties (2020) · cites this paper as Lee et al., 2005
In the citing paper
“Also, they explored the novel object more than the familiar ones, as an indication for object recognition (Hunsaker et al., 2007a; Lee et al., 2005; Vago and Kesner, 2008).”
From The medial prefrontal cortex - hippocampus circuit that integrates information of object, place and time to construct episodic memory in rodents: Behavioral, anatomical and neurochemical properties (2020) · cites this paper as Lee et al., 2005
Citations
Cites
McClelland, J. L., McNaughton, B. L., & O'Reilly, R. C. (1995) · Psychological Review · doi:10.1037/0033-295x.102.3.419 · Cited by 5,256
Reactivation of hippocampal ensemble memories during sleep
Wilson, M. A., & McNaughton, B. L. (1994) · Science · doi:10.1126/science.8036517 · Cited by 3,118
Simple memory: a theory for archicortex
Marr, D. (1971) · Philosophical Transactions of the Royal Society of London. B, Biological Sciences · doi:10.1098/rstb.1971.0078 · Cited by 2,771
de Nó, R. L. (1934) · Cited by 1,974
Regional dissociations within the hippocampus-memory and anxiety
Bannerman, D. M., Rawlins, J. N. P., McHugh, S. B., Deacon, R. M. J., Yee, B. K., Bast, T., Zhang, W.-N., Pothuizen, H. H. J., & Feldon, J. (2004) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2004.03.004 · Cited by 1,462
Hippocampal synaptic enhancement and information storage within a distributed memory system
McNaughton, B. L., & Morris, R. G. M. (1987) · Trends in Neurosciences · doi:10.1016/0166-2236(87)90011-7 · Cited by 1,304
Computational analysis of the role of the hippocampus in memory
Treves, A., & Rolls, E. T. (1994) · Hippocampus · doi:10.1002/hipo.450040319 · Cited by 1,272
Temporally structured replay of awake hippocampal ensemble activity during rapid eye movement sleep
Louie, K., & Wilson, M. A. (2001) · Neuron · doi:10.1016/s0896-6273(01)00186-6 · Cited by 1,148
Hippocampal conjunctive encoding, storage, and recall: Avoiding a trade‐off
O'Reilly, R. C., & McClelland, J. L. (1994) · Hippocampus · doi:10.1002/hipo.450040605 · Cited by 914
Contribution of human hippocampal region to novelty detection
Knight, R. T. (1996) · Nature · doi:10.1038/383256a0 · Cited by 848
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da Luz, A. C. D. D. S., Dias, G. P., Bevilaqua, M. C. D. N., Cocks, G. D., Gardino, P. F., Thuret, S., & Nardi, A. E. (2013) · Neuropsychobiology · doi:10.1159/000353269 · Cited by 4,015
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Lisman, J. E., & Grace, A. A. (2005) · Neuron · doi:10.1016/j.neuron.2005.05.002 · Cited by 1,983
Heldt, S. A., Stanek, L., Chhatwal, J. P., & Ressler, K. J. (2007) · Molecular Psychiatry · doi:10.1038/sj.mp.4001957 · Cited by 684
Messaoudi, E., Kanhema, T., Soule, J. D., Tiron, A., Dagytė, G., da Silva, B., & Bramham, C. R. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.2883-07.2007 · Cited by 472
Assessment of spatial memory in mice
Sharma, S., Rakoczy, S. G., & Brown‐Borg, H. M. (2010) · Life Sciences · doi:10.1016/j.lfs.2010.09.004 · Cited by 399
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Eichenbaum, H., Sauvage, M., Fortin, N., Komorowski, R., & Lipton, P. (2012) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2011.07.006 · Cited by 354
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Self-citationHippocampal long-term depression: master or minion in declarative memory processes?
Kemp, A., & Manahan-Vaughan, D. (2007) · Trends in Neurosciences · doi:10.1016/j.tins.2007.01.002 · Cited by 336
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Neural circuitry for rat recognition memory
Warburton, E. C., & Brown, M. W. (2014) · Behavioural Brain Research · doi:10.1016/j.bbr.2014.09.050 · Cited by 331
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Olsen, R. K., Moses, S. N., Riggs, L., & Ryan, J. D. (2012) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2012.00146 · Cited by 348
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Hasselmo, M. E., & Eichenbaum, H. (2005) · Neural Networks · doi:10.1016/j.neunet.2005.08.007 · Cited by 310
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Kumaran, D., & Maguire, E. A. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.1677-07.2007 · Cited by 264
Duncan, K. D., Ketz, N., Inati, S., & Davachi, L. (2011) · Hippocampus · doi:10.1002/hipo.20933 · Cited by 284
The role of the dentate gyrus, CA3a,b, and CA3c for detecting spatial and environmental novelty
Hunsaker, M. R., Rosenberg, J. S., & Kesner, R. P. (2008) · Hippocampus · doi:10.1002/hipo.20464 · Cited by 252
Self-citationPattern separation, pattern completion, and new neuronal codes within a continuous CA3 map
Leutgeb, S., & Leutgeb, J. K. (2007) · Learning & Memory · doi:10.1101/lm.703907 · Cited by 234
Distinct roles of medial and lateral entorhinal cortex in spatial cognition
Van Cauter, T., Camon, J., Alvernhe, A., Elduayen, C., Sargolini, F., & Save, E. (2013) · Cerebral Cortex · doi:10.1093/cercor/bhs033 · Cited by 196
Mustafa, S., Walker, A. J., Bennett, G., & Wigmore, P. M. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06325.x · Cited by 193
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Palchykova, S., Winsky‐Sommerer, R., Meerlo, P., Dürr, R., & Tobler, I. (2006) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2005.11.005 · Cited by 192
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Koehl, M., & Abrous, D. N. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07609.x · Cited by 198
VanElzakker, M. B., Fevurly, R. D., Breindel, T., & Spencer, R. L. (2008) · Learning & Memory · doi:10.1101/lm.1196508 · Cited by 179
Ito, R., & Lee, A. C. H. (2016) · Behavioural Brain Research · doi:10.1016/j.bbr.2016.07.039 · Cited by 188
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Escamilla, C. O., Filonova, I., Walker, A. K., Xuan, Z. X., Holehonnur, R., Espinosa, F., Liu, S., Thyme, S. B., López-García, I. A., Mendoza, D. B., et al. (2017) · Nature · doi:10.1038/nature24470 · Cited by 165
Gilbert, P. E., & Brushfield, A. M. (2009) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2009.03.037 · Cited by 172
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Hagena, H., Hansen, N., & Manahan‐Vaughan, D. (2016) · Cerebral Cortex · doi:10.1093/cercor/bhv330 · Cited by 174
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Langston, R. F., Stevenson, C. H., Wilson, C. L., Saunders, I., & Wood, E. R. (2010) · Behavioural Brain Research · doi:10.1016/j.bbr.2010.07.006 · Cited by 161
Chao, O. Y., de Souza Silva, M. A., Yang, Y.-M., & Huston, J. P. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.04.007 · Cited by 158
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Heaney, C. F., & Kinney, J. W. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.01.007 · Cited by 162
Jaramillo, T. C., Speed, H. E., Xuan, Z., Reimers, J. M., Liu, S., & Powell, C. M. (2015) · Autism Research · doi:10.1002/aur.1529 · Cited by 160
Wigmore, P. M., Mustafa, S., ELBeltagy, M., Lyons, L., Umka, J., & Bennett, G. (2010) · Advances in experimental medicine and biology · doi:10.1007/978-1-4419-6306-2_20 · Cited by 148
Mueller, S. G., Chao, L. L., Berman, B. D., & Weiner, M. W. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.03.028 · Cited by 156
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Gobeske, K. T., Das, S., Bonaguidi, M. A., Weiss, C., Radulović, J., Disterhoft, J. F., & Kessler, J. A. (2009) · PLoS ONE · doi:10.1371/journal.pone.0007506 · Cited by 128
Rogers, J. L., Santis, S. D., & See, R. E. (2008) · Psychopharmacology · doi:10.1007/s00213-008-1187-7 · Cited by 121
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Umka, J., Mustafa, S., ELBeltagy, M., Thorpe, A., Latif, L., Bennett, G., & Wigmore, P. M. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.11.073 · Cited by 120
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Goh, J. J., & Manahan‐Vaughan, D. (2012) · Cerebral Cortex · doi:10.1093/cercor/bhs089 · Cited by 116
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Pauli, E., Hildebrandt, M. A. T., Romstöck, J., Stefan, H., & Blümcke, I. (2006) · Neurology · doi:10.1212/01.wnl.0000239828.36651.73 · Cited by 113
Lyons, L., ELBeltagy, M., Umka, J., Markwick, R., Startin, C. M., Bennett, G., & Wigmore, P. M. (2010) · Psychopharmacology · doi:10.1007/s00213-010-2122-2 · Cited by 108
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Self-citationSchumacher, A., Villaruel, F. R., Ussling, A., Riaz, S., Lee, A. C. H., & Ito, R. (2018) · Current Biology · doi:10.1016/j.cub.2018.03.012 · Cited by 101
Evaluating the temporal context of episodic memory: The role of CA3 and CA1
Hunsaker, M. R. (2007) · Behavioural Brain Research · doi:10.1016/j.bbr.2007.11.015 · Cited by 101
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Lee, I., & Solivan, F. (2008) · Learning & Memory · doi:10.1101/lm.902708 · Cited by 106
Self-citationKabadi, S. V., Stoica, B. A., Byrnes, K. R., Hanscom, M., Loane, D. J., & Faden, A. I. (2011) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2011.117 · Cited by 96
Vago, D. R., & Kesner, R. P. (2008) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.01.002 · Cited by 100
Self-citationHansen, N., & Manahan‐Vaughan, D. (2015) · Hippocampus · doi:10.1002/hipo.22436 · Cited by 92
Hunsaker, M. R., Chen, V., Tran, G. T., & Kesner, R. P. (2013) · Hippocampus · doi:10.1002/hipo.22097 · Cited by 88
Self-citationAdult neurogenesis and the memories of drug addiction
Canales, J. J. (2007) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/s00406-007-0730-6 · Cited by 88
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O’Tuathaigh, C. M. P., O'Sullivan, G. J., Kinsella, A., Harvey, R. P., Tighe, O., Croke, D. T., & Waddington, J. L. (2005) · Neuroreport · doi:10.1097/01.wnr.0000192738.31029.0a · Cited by 79
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Spanswick, S. C., & Sutherland, R. J. (2010) · Learning & Memory · doi:10.1101/lm.1746710 · Cited by 78
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Miller, T. D., Chong, T. T. ‐., Davies, A. M. A., Johnson, M. R., Irani, S. R., Husain, M., Ng, T. W. C., Jacob, S., Maddison, P., Kennard, C., et al. (2020) · eLife · doi:10.7554/elife.41836 · Cited by 85
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Poirier, G. L., Amin, E., & Aggleton, J. P. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.4607-07.2008 · Cited by 72
Barbosa, F. F., de Oliveira Pontes, I. M., Ribeiro, S., Ribeiro, A. M., & Silva, R. H. (2012) · Behavioural Brain Research · doi:10.1016/j.bbr.2012.04.022 · Cited by 71
Deuker, L., Doeller, C. F., Fell, J., & Axmacher, N. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00064 · Cited by 80
Li, S., Fan, Y., Wang, W., & Tang, Y. (2011) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.10.007 · Cited by 71
Long, N. M., Lee, H., & Kuhl, B. A. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.1850-16.2016 · Cited by 74
Vouimba, R., Yaniv, D., & Richter‐Levin, G. (2006) · Neuropharmacology · doi:10.1016/j.neuropharm.2006.07.007 · Cited by 71
Bramham, C. R. (2007) · Progress in Brain Research · doi:10.1016/s0079-6123(07)63025-8 · Cited by 69
Cellular, molecular, and genetic substrates underlying the impact of nicotine on learning
Gould, T. J., & Leach, P. T. (2013) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2013.08.004 · Cited by 72
Hunsaker, M. R., & Kesner, R. P. (2017) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2017.11.012 · Cited by 69
Self-citationCyclin D1 Gene Ablation Confers Neuroprotection in Traumatic Brain Injury
Kabadi, S. V., Stoica, B. A., Loane, D. J., Byrnes, K. R., Hanscom, M., Cabatbat, R. M., Tan, M. T., & Faden, A. I. (2011) · Journal of Neurotrauma · doi:10.1089/neu.2011.1980 · Cited by 66
Bath, K. G., Nitenson, A. S., Lichtman, E. S., Lopez, C., Chen, W., Gallo, M. E., Goodwill, H. L., & Manzano-Nieves, G. (2017) · Neurobiology of Stress · doi:10.1016/j.ynstr.2017.04.001 · Cited by 66
Maâroufi, K., Had‐Aissouni, L., Melon, C., Sakly, M., Abdelmelek, H., Poucet, B., & Save, É. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.10.016 · Cited by 66
Nicotinic ACh Receptors in the Hippocampus: Role in Excitability and Plasticity
Yakel, J. L. (2012) · Nicotine & Tobacco Research · doi:10.1093/ntr/nts091 · Cited by 65
Morellini, F., Lepsveridze, E., Kähler, B., Dityatev, A. E., & Schachner, M. (2006) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2006.10.006 · Cited by 61
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Alexander, J. C., McDermott, C. M., Tunur, T., Rands, V. F., Stelly, C. E., Karhson, D. S., Bowlby, M. R., An, W., Sweatt, J. D., & Schrader, L. A. (2009) · Learning & Memory · doi:10.1101/lm.1261709 · Cited by 62
Behavioral profile of a heterozygous mutant mouse model for EGF-like domain neuregulin 1.
Duffy, L., Cappas, E., Scimone, A., Schofield, P. R., & Karl, T. (2008) · Behavioral Neuroscience · doi:10.1037/0735-7044.122.4.748 · Cited by 59
Developmental onset distinguishes three types of spontaneous recognition memory in mice
Cruz-Sanchez, A., Dematagoda, S., Ahmed, R., Mohanathaas, S., Odenwald, N., & Arruda-Carvalho, M. (2020) · Scientific Reports · doi:10.1038/s41598-020-67619-w · Cited by 58
Role of the dorsal hippocampus in object memory load
Sannino, S., Russo, F., Torromino, G., Pendolino, V., Calabresi, P., & De Leonibus, E. (2012) · Learning & Memory · doi:10.1101/lm.025213.111 · Cited by 57
Kabadi, S. V., Stoica, B. A., Hanscom, M., Loane, D. J., Kharebava, G., Murray, M. G., II, Cabatbat, R. M., & Faden, A. I. (2011) · Neurotherapeutics · doi:10.1007/s13311-011-0095-4 · Cited by 59
Pace, T. W. W., Gaylord, R. I., Topczewski, F., Girotti, M., Rubin, B., & Spencer, R. L. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04354.x · Cited by 59
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Atienza, M., da Silva, K. C. A., González‐Escamilla, G., Gil-Neciga, E., Gonzalez, A. S., & Cantero, J. L. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.05.047 · Cited by 57
Circuit-based interventions in the dentate gyrus rescue epilepsy-associated cognitive dysfunction
Kahn, J. B., Port, R. G., Yue, C., Takano, H., & Coulter, D. A. (2019) · Brain · doi:10.1093/brain/awz209 · Cited by 57
Human hippocampal processing of environmental novelty during spatial navigation
Kaplan, R., Horner, A. J., Bandettini, P. A., Doeller, C. F., & Burgess, N. (2014) · Hippocampus · doi:10.1002/hipo.22264 · Cited by 56
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Mendez, M., Arias, N., Uceda, S., & Arias, J. L. (2015) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2015.07.004 · Cited by 54
Binder, S., Dere, E., & Zlomuzica, A. (2015) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2015.04.002 · Cited by 56
Mueller, S. G., Laxer, K. D., Scanlon, C., Garcia, P. A., McMullen, W. J., Loring, D. W., Meador, K. J., & Weiner, M. W. (2011) · Human Brain Mapping · doi:10.1002/hbm.21226 · Cited by 56
Zhao, Q., Murakami, Y., Tohda, M., Obi, R., Shimada, Y., & Matsumoto, K. (2007) · Journal of Pharmacological Sciences · doi:10.1254/jphs.fp0061457 · Cited by 51
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Fredes, F., & Shigemoto, R. (2021) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2021.107486 · Cited by 52
Christiansen, K., Dillingham, C. M., Wright, N. F., Saunders, R. C., Vann, S. D., & Aggleton, J. P. (2016) · European Journal of Neuroscience · doi:10.1111/ejn.13208 · Cited by 52
The importance of the rat hippocampus for learning the structure of visual arrays
Sanderson, D. J., Pearce, J. M., Kyd, R. J., & Aggleton, J. P. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.05035.x · Cited by 49
Brown, T. I., Hasselmo, M. E., & Stern, C. E. (2014) · Hippocampus · doi:10.1002/hipo.22273 · Cited by 51
Metadata
- Authors
- Lee, I., Hunsaker, M. R., & Kesner, R. P.
- Affiliations
- Boston University (US)
- University of Utah (US)
- Venue
- Behavioral Neuroscience
- Published
- 2005
- Volume
- 119
- Issue
- 1
- Pages
- 145-153
- ISSN
- 0735-7044 (ISSN-L)
- 1939-0084
- OpenAlex
- W2154243350
- Cited by
- 270
- References
- 51
- Citations by year
- 2026: 3 · 2025: 3 · 2024: 10 · 2023: 5 · 2022: 8 · 2021: 11 · 2020: 7 · 2019: 8 · 2018: 13 · 2017: 14 · 2016: 14 · 2015: 15 · 2014: 17 · 2013: 17 · 2012: 19
- FWCI
- 8.57
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Behavioral Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- hippocampal subfields, dorsal hippocampus, dentate gyrus, CA1, CA3, neurotoxic lesion, spatial memory, novel object recognition
- MeSH terms
- Animals, Cognition, Exploratory Behavior, Hippocampus, Male, Space Perception, Rats, Long-Evans, Rats
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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