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gin commit from Saksham

New files: 218
Modified files: 1
Saksham Sharda 3 년 전
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7341a55b83
100개의 변경된 파일2181개의 추가작업 그리고 9개의 파일을 삭제
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ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170307_154746_concat/ephys/sub-MS10_ses-Peter_MS10_170307_154746_concat_channels.tsv → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170307154746concat/ephys/sub-MS10_ses-PeterMS10170307154746concat_channels.tsv


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170307_154746_concat/ephys/sub-MS10_ses-Peter_MS10_170307_154746_concat_contacts.tsv → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170307154746concat/ephys/sub-MS10_ses-PeterMS10170307154746concat_contacts.tsv


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170307_154746_concat/ephys/sub-MS10_ses-Peter_MS10_170307_154746_concat_ephys.json → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170307154746concat/ephys/sub-MS10_ses-PeterMS10170307154746concat_ephys.json


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170307_154746_concat/ephys/sub-MS10_ses-Peter_MS10_170307_154746_concat_ephys.nwb → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170307154746concat/ephys/sub-MS10_ses-PeterMS10170307154746concat_ephys.nwb


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170307_154746_concat/ephys/sub-MS10_ses-Peter_MS10_170307_154746_concat_probes.tsv → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170307154746concat/ephys/sub-MS10_ses-PeterMS10170307154746concat_probes.tsv


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170311_180956_concat/ephys/sub-MS10_ses-Peter_MS10_170311_180956_concat_channels.tsv → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170311180956concat/ephys/sub-MS10_ses-PeterMS10170311180956concat_channels.tsv


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170311_180956_concat/ephys/sub-MS10_ses-Peter_MS10_170311_180956_concat_contacts.tsv → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170311180956concat/ephys/sub-MS10_ses-PeterMS10170311180956concat_contacts.tsv


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170311_180956_concat/ephys/sub-MS10_ses-Peter_MS10_170311_180956_concat_ephys.json → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170311180956concat/ephys/sub-MS10_ses-PeterMS10170311180956concat_ephys.json


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170311_180956_concat/ephys/sub-MS10_ses-Peter_MS10_170311_180956_concat_ephys.nwb → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170311180956concat/ephys/sub-MS10_ses-PeterMS10170311180956concat_ephys.nwb


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170311_180956_concat/ephys/sub-MS10_ses-Peter_MS10_170311_180956_concat_probes.tsv → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170311180956concat/ephys/sub-MS10_ses-PeterMS10170311180956concat_probes.tsv


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170313_122631_concat/ephys/sub-MS10_ses-Peter_MS10_170313_122631_concat_channels.tsv → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170313122631concat/ephys/sub-MS10_ses-PeterMS10170313122631concat_channels.tsv


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170313_122631_concat/ephys/sub-MS10_ses-Peter_MS10_170313_122631_concat_contacts.tsv → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170313122631concat/ephys/sub-MS10_ses-PeterMS10170313122631concat_contacts.tsv


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170313_122631_concat/ephys/sub-MS10_ses-Peter_MS10_170313_122631_concat_ephys.json → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170313122631concat/ephys/sub-MS10_ses-PeterMS10170313122631concat_ephys.json


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170313_122631_concat/ephys/sub-MS10_ses-Peter_MS10_170313_122631_concat_ephys.nwb → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170313122631concat/ephys/sub-MS10_ses-PeterMS10170313122631concat_ephys.nwb


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170313_122631_concat/ephys/sub-MS10_ses-Peter_MS10_170313_122631_concat_probes.tsv → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170313122631concat/ephys/sub-MS10_ses-PeterMS10170313122631concat_probes.tsv


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170314_163038/ephys/sub-MS10_ses-Peter_MS10_170314_163038_channels.tsv → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170314163038/ephys/sub-MS10_ses-PeterMS10170314163038_channels.tsv


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170314_163038/ephys/sub-MS10_ses-Peter_MS10_170314_163038_contacts.tsv → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170314163038/ephys/sub-MS10_ses-PeterMS10170314163038_contacts.tsv


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170314_163038/ephys/sub-MS10_ses-Peter_MS10_170314_163038_ephys.json → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170314163038/ephys/sub-MS10_ses-PeterMS10170314163038_ephys.json


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170314_163038/ephys/sub-MS10_ses-Peter_MS10_170314_163038_ephys.nwb → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170314163038/ephys/sub-MS10_ses-PeterMS10170314163038_ephys.nwb


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170314_163038/ephys/sub-MS10_ses-Peter_MS10_170314_163038_probes.tsv → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170314163038/ephys/sub-MS10_ses-PeterMS10170314163038_probes.tsv


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170317_153237_concat/ephys/sub-MS10_ses-Peter_MS10_170317_153237_concat_channels.tsv → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170317153237concat/ephys/sub-MS10_ses-PeterMS10170317153237concat_channels.tsv


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170317_153237_concat/ephys/sub-MS10_ses-Peter_MS10_170317_153237_concat_contacts.tsv → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170317153237concat/ephys/sub-MS10_ses-PeterMS10170317153237concat_contacts.tsv


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170317_153237_concat/ephys/sub-MS10_ses-Peter_MS10_170317_153237_concat_ephys.json → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170317153237concat/ephys/sub-MS10_ses-PeterMS10170317153237concat_ephys.json


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170317_153237_concat/ephys/sub-MS10_ses-Peter_MS10_170317_153237_concat_ephys.nwb → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170317153237concat/ephys/sub-MS10_ses-PeterMS10170317153237concat_ephys.nwb


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170317_153237_concat/ephys/sub-MS10_ses-Peter_MS10_170317_153237_concat_probes.tsv → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170317153237concat/ephys/sub-MS10_ses-PeterMS10170317153237concat_probes.tsv


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170319_180352_concat/ephys/sub-MS10_ses-Peter_MS10_170319_180352_concat_channels.tsv → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170319180352concat/ephys/sub-MS10_ses-PeterMS10170319180352concat_channels.tsv


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170319_180352_concat/ephys/sub-MS10_ses-Peter_MS10_170319_180352_concat_contacts.tsv → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170319180352concat/ephys/sub-MS10_ses-PeterMS10170319180352concat_contacts.tsv


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170319_180352_concat/ephys/sub-MS10_ses-Peter_MS10_170319_180352_concat_ephys.json → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170319180352concat/ephys/sub-MS10_ses-PeterMS10170319180352concat_ephys.json


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170319_180352_concat/ephys/sub-MS10_ses-Peter_MS10_170319_180352_concat_ephys.nwb → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170319180352concat/ephys/sub-MS10_ses-PeterMS10170319180352concat_ephys.nwb


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170319_180352_concat/ephys/sub-MS10_ses-Peter_MS10_170319_180352_concat_probes.tsv → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170319180352concat/ephys/sub-MS10_ses-PeterMS10170319180352concat_probes.tsv


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170320_212321_concat/ephys/sub-MS10_ses-Peter_MS10_170320_212321_concat_channels.tsv → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170320212321concat/ephys/sub-MS10_ses-PeterMS10170320212321concat_channels.tsv


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170320_212321_concat/ephys/sub-MS10_ses-Peter_MS10_170320_212321_concat_contacts.tsv → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170320212321concat/ephys/sub-MS10_ses-PeterMS10170320212321concat_contacts.tsv


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170320_212321_concat/ephys/sub-MS10_ses-Peter_MS10_170320_212321_concat_ephys.json → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170320212321concat/ephys/sub-MS10_ses-PeterMS10170320212321concat_ephys.json


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170320_212321_concat/ephys/sub-MS10_ses-Peter_MS10_170320_212321_concat_ephys.nwb → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170320212321concat/ephys/sub-MS10_ses-PeterMS10170320212321concat_ephys.nwb


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170320_212321_concat/ephys/sub-MS10_ses-Peter_MS10_170320_212321_concat_probes.tsv → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170320212321concat/ephys/sub-MS10_ses-PeterMS10170320212321concat_probes.tsv


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170321_164406_concat/ephys/sub-MS10_ses-Peter_MS10_170321_164406_concat_channels.tsv → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170321164406concat/ephys/sub-MS10_ses-PeterMS10170321164406concat_channels.tsv


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170321_164406_concat/ephys/sub-MS10_ses-Peter_MS10_170321_164406_concat_contacts.tsv → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170321164406concat/ephys/sub-MS10_ses-PeterMS10170321164406concat_contacts.tsv


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170321_164406_concat/ephys/sub-MS10_ses-Peter_MS10_170321_164406_concat_ephys.json → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170321164406concat/ephys/sub-MS10_ses-PeterMS10170321164406concat_ephys.json


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170321_164406_concat/ephys/sub-MS10_ses-Peter_MS10_170321_164406_concat_ephys.nwb → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170321164406concat/ephys/sub-MS10_ses-PeterMS10170321164406concat_ephys.nwb


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170321_164406_concat/ephys/sub-MS10_ses-Peter_MS10_170321_164406_concat_probes.tsv → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170321164406concat/ephys/sub-MS10_ses-PeterMS10170321164406concat_probes.tsv


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170323_173246/ephys/sub-MS10_ses-Peter_MS10_170323_173246_channels.tsv → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170323173246/ephys/sub-MS10_ses-PeterMS10170323173246_channels.tsv


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170323_173246/ephys/sub-MS10_ses-Peter_MS10_170323_173246_contacts.tsv → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170323173246/ephys/sub-MS10_ses-PeterMS10170323173246_contacts.tsv


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170323_173246/ephys/sub-MS10_ses-Peter_MS10_170323_173246_ephys.json → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170323173246/ephys/sub-MS10_ses-PeterMS10170323173246_ephys.json


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170323_173246/ephys/sub-MS10_ses-Peter_MS10_170323_173246_ephys.nwb → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170323173246/ephys/sub-MS10_ses-PeterMS10170323173246_ephys.nwb


ephys_nwb_petersen/sub-MS10/ses-Peter_MS10_170323_173246/ephys/sub-MS10_ses-Peter_MS10_170323_173246_probes.tsv → ephys_nwb_petersen/sub-MS10/ses-PeterMS10170323173246/ephys/sub-MS10_ses-PeterMS10170323173246_probes.tsv


+ 9 - 9
ephys_nwb_petersen/sub-MS10/sub-MS10_sessions.tsv

@@ -1,10 +1,10 @@
 session_id	#_trials	comment
-ses-Peter_MS10_170320_212321_concat	179.0	Petersen et al. demonstrate that cooling of the medial septum slows theta oscillation and increases choice errors without affecting spatial features of pyramidal neurons. Cooling affects distance-time, but not distance-theta phase, compression. The findings reveal that cell assemblies are organized by theta phase and not by external (clock) time.
-ses-Peter_MS10_170311_180956_concat		Petersen et al. demonstrate that cooling of the medial septum slows theta oscillation and increases choice errors without affecting spatial features of pyramidal neurons. Cooling affects distance-time, but not distance-theta phase, compression. The findings reveal that cell assemblies are organized by theta phase and not by external (clock) time.
-ses-Peter_MS10_170307_154746_concat		Petersen et al. demonstrate that cooling of the medial septum slows theta oscillation and increases choice errors without affecting spatial features of pyramidal neurons. Cooling affects distance-time, but not distance-theta phase, compression. The findings reveal that cell assemblies are organized by theta phase and not by external (clock) time.
-ses-Peter_MS10_170314_163038	142.0	Petersen et al. demonstrate that cooling of the medial septum slows theta oscillation and increases choice errors without affecting spatial features of pyramidal neurons. Cooling affects distance-time, but not distance-theta phase, compression. The findings reveal that cell assemblies are organized by theta phase and not by external (clock) time.
-ses-Peter_MS10_170317_153237_concat	201.0	Petersen et al. demonstrate that cooling of the medial septum slows theta oscillation and increases choice errors without affecting spatial features of pyramidal neurons. Cooling affects distance-time, but not distance-theta phase, compression. The findings reveal that cell assemblies are organized by theta phase and not by external (clock) time.
-ses-Peter_MS10_170319_180352_concat		Petersen et al. demonstrate that cooling of the medial septum slows theta oscillation and increases choice errors without affecting spatial features of pyramidal neurons. Cooling affects distance-time, but not distance-theta phase, compression. The findings reveal that cell assemblies are organized by theta phase and not by external (clock) time.
-ses-Peter_MS10_170313_122631_concat		Petersen et al. demonstrate that cooling of the medial septum slows theta oscillation and increases choice errors without affecting spatial features of pyramidal neurons. Cooling affects distance-time, but not distance-theta phase, compression. The findings reveal that cell assemblies are organized by theta phase and not by external (clock) time.
-ses-Peter_MS10_170323_173246	154.0	Petersen et al. demonstrate that cooling of the medial septum slows theta oscillation and increases choice errors without affecting spatial features of pyramidal neurons. Cooling affects distance-time, but not distance-theta phase, compression. The findings reveal that cell assemblies are organized by theta phase and not by external (clock) time.
-ses-Peter_MS10_170321_164406_concat	130.0	Petersen et al. demonstrate that cooling of the medial septum slows theta oscillation and increases choice errors without affecting spatial features of pyramidal neurons. Cooling affects distance-time, but not distance-theta phase, compression. The findings reveal that cell assemblies are organized by theta phase and not by external (clock) time.
+ses-PeterMS10170307154746concat		Petersen et al. demonstrate that cooling of the medial septum slows theta oscillation and increases choice errors without affecting spatial features of pyramidal neurons. Cooling affects distance-time, but not distance-theta phase, compression. The findings reveal that cell assemblies are organized by theta phase and not by external (clock) time.
+ses-PeterMS10170311180956concat		Petersen et al. demonstrate that cooling of the medial septum slows theta oscillation and increases choice errors without affecting spatial features of pyramidal neurons. Cooling affects distance-time, but not distance-theta phase, compression. The findings reveal that cell assemblies are organized by theta phase and not by external (clock) time.
+ses-PeterMS10170313122631concat		Petersen et al. demonstrate that cooling of the medial septum slows theta oscillation and increases choice errors without affecting spatial features of pyramidal neurons. Cooling affects distance-time, but not distance-theta phase, compression. The findings reveal that cell assemblies are organized by theta phase and not by external (clock) time.
+ses-PeterMS10170314163038	142.0	Petersen et al. demonstrate that cooling of the medial septum slows theta oscillation and increases choice errors without affecting spatial features of pyramidal neurons. Cooling affects distance-time, but not distance-theta phase, compression. The findings reveal that cell assemblies are organized by theta phase and not by external (clock) time.
+ses-PeterMS10170317153237concat	201.0	Petersen et al. demonstrate that cooling of the medial septum slows theta oscillation and increases choice errors without affecting spatial features of pyramidal neurons. Cooling affects distance-time, but not distance-theta phase, compression. The findings reveal that cell assemblies are organized by theta phase and not by external (clock) time.
+ses-PeterMS10170319180352concat		Petersen et al. demonstrate that cooling of the medial septum slows theta oscillation and increases choice errors without affecting spatial features of pyramidal neurons. Cooling affects distance-time, but not distance-theta phase, compression. The findings reveal that cell assemblies are organized by theta phase and not by external (clock) time.
+ses-PeterMS10170320212321concat	179.0	Petersen et al. demonstrate that cooling of the medial septum slows theta oscillation and increases choice errors without affecting spatial features of pyramidal neurons. Cooling affects distance-time, but not distance-theta phase, compression. The findings reveal that cell assemblies are organized by theta phase and not by external (clock) time.
+ses-PeterMS10170321164406concat	130.0	Petersen et al. demonstrate that cooling of the medial septum slows theta oscillation and increases choice errors without affecting spatial features of pyramidal neurons. Cooling affects distance-time, but not distance-theta phase, compression. The findings reveal that cell assemblies are organized by theta phase and not by external (clock) time.
+ses-PeterMS10170323173246	154.0	Petersen et al. demonstrate that cooling of the medial septum slows theta oscillation and increases choice errors without affecting spatial features of pyramidal neurons. Cooling affects distance-time, but not distance-theta phase, compression. The findings reveal that cell assemblies are organized by theta phase and not by external (clock) time.

ephys_nwb_petersen/sub-MS12/ses-Peter_MS12_170712_101120_concat/ephys/sub-MS12_ses-Peter_MS12_170712_101120_concat_channels.tsv → ephys_nwb_petersen/sub-MS12/ses-PeterMS12170712101120concat/ephys/sub-MS12_ses-PeterMS12170712101120concat_channels.tsv


ephys_nwb_petersen/sub-MS12/ses-Peter_MS12_170712_101120_concat/ephys/sub-MS12_ses-Peter_MS12_170712_101120_concat_contacts.tsv → ephys_nwb_petersen/sub-MS12/ses-PeterMS12170712101120concat/ephys/sub-MS12_ses-PeterMS12170712101120concat_contacts.tsv


ephys_nwb_petersen/sub-MS12/ses-Peter_MS12_170712_101120_concat/ephys/sub-MS12_ses-Peter_MS12_170712_101120_concat_ephys.json → ephys_nwb_petersen/sub-MS12/ses-PeterMS12170712101120concat/ephys/sub-MS12_ses-PeterMS12170712101120concat_ephys.json


ephys_nwb_petersen/sub-MS12/ses-Peter_MS12_170712_101120_concat/ephys/sub-MS12_ses-Peter_MS12_170712_101120_concat_ephys.nwb → ephys_nwb_petersen/sub-MS12/ses-PeterMS12170712101120concat/ephys/sub-MS12_ses-PeterMS12170712101120concat_ephys.nwb


ephys_nwb_petersen/sub-MS12/ses-Peter_MS12_170712_101120_concat/ephys/sub-MS12_ses-Peter_MS12_170712_101120_concat_probes.tsv → ephys_nwb_petersen/sub-MS12/ses-PeterMS12170712101120concat/ephys/sub-MS12_ses-PeterMS12170712101120concat_probes.tsv


ephys_nwb_petersen/sub-MS12/ses-Peter_MS12_170713_093400_concat/ephys/sub-MS12_ses-Peter_MS12_170713_093400_concat_channels.tsv → ephys_nwb_petersen/sub-MS12/ses-PeterMS12170713093400concat/ephys/sub-MS12_ses-PeterMS12170713093400concat_channels.tsv


ephys_nwb_petersen/sub-MS12/ses-Peter_MS12_170713_093400_concat/ephys/sub-MS12_ses-Peter_MS12_170713_093400_concat_contacts.tsv → ephys_nwb_petersen/sub-MS12/ses-PeterMS12170713093400concat/ephys/sub-MS12_ses-PeterMS12170713093400concat_contacts.tsv


ephys_nwb_petersen/sub-MS12/ses-Peter_MS12_170713_093400_concat/ephys/sub-MS12_ses-Peter_MS12_170713_093400_concat_ephys.json → ephys_nwb_petersen/sub-MS12/ses-PeterMS12170713093400concat/ephys/sub-MS12_ses-PeterMS12170713093400concat_ephys.json


ephys_nwb_petersen/sub-MS12/ses-Peter_MS12_170713_093400_concat/ephys/sub-MS12_ses-Peter_MS12_170713_093400_concat_ephys.nwb → ephys_nwb_petersen/sub-MS12/ses-PeterMS12170713093400concat/ephys/sub-MS12_ses-PeterMS12170713093400concat_ephys.nwb


+ 2 - 0
ephys_nwb_petersen/sub-MS12/ses-PeterMS12170713093400concat/ephys/sub-MS12_ses-PeterMS12170713093400concat_probes.tsv

@@ -0,0 +1,2 @@
+probeID	type
+Device	acute

ephys_nwb_petersen/sub-MS12/ses-Peter_MS12_170714_122034_concat/ephys/sub-MS12_ses-Peter_MS12_170714_122034_concat_channels.tsv → ephys_nwb_petersen/sub-MS12/ses-PeterMS12170714122034concat/ephys/sub-MS12_ses-PeterMS12170714122034concat_channels.tsv


+ 129 - 0
ephys_nwb_petersen/sub-MS12/ses-PeterMS12170714122034concat/ephys/sub-MS12_ses-PeterMS12170714122034concat_contacts.tsv

@@ -0,0 +1,129 @@
+impedance	contact_id	probe_id	Location
+-1.0	0	Device	unknown
+-1.0	1	Device	unknown
+-1.0	2	Device	unknown
+-1.0	3	Device	unknown
+-1.0	4	Device	unknown
+-1.0	5	Device	unknown
+-1.0	6	Device	unknown
+-1.0	7	Device	unknown
+-1.0	8	Device	unknown
+-1.0	9	Device	unknown
+-1.0	10	Device	unknown
+-1.0	11	Device	unknown
+-1.0	12	Device	unknown
+-1.0	13	Device	unknown
+-1.0	14	Device	unknown
+-1.0	15	Device	unknown
+-1.0	16	Device	unknown
+-1.0	17	Device	unknown
+-1.0	18	Device	unknown
+-1.0	19	Device	unknown
+-1.0	20	Device	unknown
+-1.0	21	Device	unknown
+-1.0	22	Device	unknown
+-1.0	23	Device	unknown
+-1.0	24	Device	unknown
+-1.0	25	Device	unknown
+-1.0	26	Device	unknown
+-1.0	27	Device	unknown
+-1.0	28	Device	unknown
+-1.0	29	Device	unknown
+-1.0	30	Device	unknown
+-1.0	31	Device	unknown
+-1.0	32	Device	unknown
+-1.0	33	Device	unknown
+-1.0	34	Device	unknown
+-1.0	35	Device	unknown
+-1.0	36	Device	unknown
+-1.0	37	Device	unknown
+-1.0	38	Device	unknown
+-1.0	39	Device	unknown
+-1.0	40	Device	unknown
+-1.0	41	Device	unknown
+-1.0	42	Device	unknown
+-1.0	43	Device	unknown
+-1.0	44	Device	unknown
+-1.0	45	Device	unknown
+-1.0	46	Device	unknown
+-1.0	47	Device	unknown
+-1.0	48	Device	unknown
+-1.0	49	Device	unknown
+-1.0	50	Device	unknown
+-1.0	51	Device	unknown
+-1.0	52	Device	unknown
+-1.0	53	Device	unknown
+-1.0	54	Device	unknown
+-1.0	55	Device	unknown
+-1.0	56	Device	unknown
+-1.0	57	Device	unknown
+-1.0	58	Device	unknown
+-1.0	59	Device	unknown
+-1.0	60	Device	unknown
+-1.0	61	Device	unknown
+-1.0	62	Device	unknown
+-1.0	63	Device	unknown
+-1.0	64	Device	unknown
+-1.0	65	Device	unknown
+-1.0	66	Device	unknown
+-1.0	67	Device	unknown
+-1.0	68	Device	unknown
+-1.0	69	Device	unknown
+-1.0	70	Device	unknown
+-1.0	71	Device	unknown
+-1.0	72	Device	unknown
+-1.0	73	Device	unknown
+-1.0	74	Device	unknown
+-1.0	75	Device	unknown
+-1.0	76	Device	unknown
+-1.0	77	Device	unknown
+-1.0	78	Device	unknown
+-1.0	79	Device	unknown
+-1.0	80	Device	unknown
+-1.0	81	Device	unknown
+-1.0	82	Device	unknown
+-1.0	83	Device	unknown
+-1.0	84	Device	unknown
+-1.0	85	Device	unknown
+-1.0	86	Device	unknown
+-1.0	87	Device	unknown
+-1.0	88	Device	unknown
+-1.0	89	Device	unknown
+-1.0	90	Device	unknown
+-1.0	91	Device	unknown
+-1.0	92	Device	unknown
+-1.0	93	Device	unknown
+-1.0	94	Device	unknown
+-1.0	95	Device	unknown
+-1.0	96	Device	unknown
+-1.0	97	Device	unknown
+-1.0	98	Device	unknown
+-1.0	99	Device	unknown
+-1.0	100	Device	unknown
+-1.0	101	Device	unknown
+-1.0	102	Device	unknown
+-1.0	103	Device	unknown
+-1.0	104	Device	unknown
+-1.0	105	Device	unknown
+-1.0	106	Device	unknown
+-1.0	107	Device	unknown
+-1.0	108	Device	unknown
+-1.0	109	Device	unknown
+-1.0	110	Device	unknown
+-1.0	111	Device	unknown
+-1.0	112	Device	unknown
+-1.0	113	Device	unknown
+-1.0	114	Device	unknown
+-1.0	115	Device	unknown
+-1.0	116	Device	unknown
+-1.0	117	Device	unknown
+-1.0	118	Device	unknown
+-1.0	119	Device	unknown
+-1.0	120	Device	unknown
+-1.0	121	Device	unknown
+-1.0	122	Device	unknown
+-1.0	123	Device	unknown
+-1.0	124	Device	unknown
+-1.0	125	Device	unknown
+-1.0	126	Device	unknown
+-1.0	127	Device	unknown

ephys_nwb_petersen/sub-MS12/ses-Peter_MS12_170714_122034_concat/ephys/sub-MS12_ses-Peter_MS12_170714_122034_concat_ephys.json → ephys_nwb_petersen/sub-MS12/ses-PeterMS12170714122034concat/ephys/sub-MS12_ses-PeterMS12170714122034concat_ephys.json


+ 1 - 0
ephys_nwb_petersen/sub-MS12/ses-PeterMS12170714122034concat/ephys/sub-MS12_ses-PeterMS12170714122034concat_ephys.nwb

@@ -0,0 +1 @@
+/annex/objects/MD5-s248208--eebfa5d8690d0751b6c36fdaf3deaa32

+ 2 - 0
ephys_nwb_petersen/sub-MS12/ses-PeterMS12170714122034concat/ephys/sub-MS12_ses-PeterMS12170714122034concat_probes.tsv

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ephys_nwb_petersen/sub-MS12/ses-PeterMS12170716172307concat/ephys/sub-MS12_ses-PeterMS12170716172307concat_channels.tsv

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ephys_nwb_petersen/sub-MS12/ses-PeterMS12170716172307concat/ephys/sub-MS12_ses-PeterMS12170716172307concat_contacts.tsv

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ephys_nwb_petersen/sub-MS12/ses-PeterMS12170716172307concat/ephys/sub-MS12_ses-PeterMS12170716172307concat_ephys.json

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ephys_nwb_petersen/sub-MS12/ses-PeterMS12170716172307concat/ephys/sub-MS12_ses-PeterMS12170716172307concat_ephys.nwb

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ephys_nwb_petersen/sub-MS12/ses-PeterMS12170716172307concat/ephys/sub-MS12_ses-PeterMS12170716172307concat_probes.tsv

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ephys_nwb_petersen/sub-MS12/ses-PeterMS12170717111614concat/ephys/sub-MS12_ses-PeterMS12170717111614concat_channels.tsv

@@ -0,0 +1,129 @@
+channel_id	Contact_id	type	units	sampling_frequency	unit_conversion_multiplier
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+87	87	neural signal	volts	20000.0	1.9499999999999999e-07
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+121	121	neural signal	volts	20000.0	1.9499999999999999e-07
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+123	123	neural signal	volts	20000.0	1.9499999999999999e-07
+124	124	neural signal	volts	20000.0	1.9499999999999999e-07
+125	125	neural signal	volts	20000.0	1.9499999999999999e-07
+126	126	neural signal	volts	20000.0	1.9499999999999999e-07
+127	127	neural signal	volts	20000.0	1.9499999999999999e-07

+ 129 - 0
ephys_nwb_petersen/sub-MS12/ses-PeterMS12170717111614concat/ephys/sub-MS12_ses-PeterMS12170717111614concat_contacts.tsv

@@ -0,0 +1,129 @@
+impedance	contact_id	probe_id	Location
+-1.0	0	Device	unknown
+-1.0	1	Device	unknown
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ephys_nwb_petersen/sub-MS12/ses-PeterMS12170717111614concat/ephys/sub-MS12_ses-PeterMS12170717111614concat_ephys.json

@@ -0,0 +1 @@
+{"PowerLineFrequency": 60.0}

+ 1 - 0
ephys_nwb_petersen/sub-MS12/ses-PeterMS12170717111614concat/ephys/sub-MS12_ses-PeterMS12170717111614concat_ephys.nwb

@@ -0,0 +1 @@
+/annex/objects/MD5-s255600--14911a8fbb12c7ce842ed9b01fe67abb

+ 2 - 0
ephys_nwb_petersen/sub-MS12/ses-PeterMS12170717111614concat/ephys/sub-MS12_ses-PeterMS12170717111614concat_probes.tsv

@@ -0,0 +1,2 @@
+probeID	type
+Device	acute

+ 129 - 0
ephys_nwb_petersen/sub-MS12/ses-PeterMS12170718101720concat/ephys/sub-MS12_ses-PeterMS12170718101720concat_channels.tsv

@@ -0,0 +1,129 @@
+channel_id	Contact_id	type	units	sampling_frequency	unit_conversion_multiplier
+0	0	neural signal	volts	20000.0	1.9499999999999999e-07
+1	1	neural signal	volts	20000.0	1.9499999999999999e-07
+2	2	neural signal	volts	20000.0	1.9499999999999999e-07
+3	3	neural signal	volts	20000.0	1.9499999999999999e-07
+4	4	neural signal	volts	20000.0	1.9499999999999999e-07
+5	5	neural signal	volts	20000.0	1.9499999999999999e-07
+6	6	neural signal	volts	20000.0	1.9499999999999999e-07
+7	7	neural signal	volts	20000.0	1.9499999999999999e-07
+8	8	neural signal	volts	20000.0	1.9499999999999999e-07
+9	9	neural signal	volts	20000.0	1.9499999999999999e-07
+10	10	neural signal	volts	20000.0	1.9499999999999999e-07
+11	11	neural signal	volts	20000.0	1.9499999999999999e-07
+12	12	neural signal	volts	20000.0	1.9499999999999999e-07
+13	13	neural signal	volts	20000.0	1.9499999999999999e-07
+14	14	neural signal	volts	20000.0	1.9499999999999999e-07
+15	15	neural signal	volts	20000.0	1.9499999999999999e-07
+16	16	neural signal	volts	20000.0	1.9499999999999999e-07
+17	17	neural signal	volts	20000.0	1.9499999999999999e-07
+18	18	neural signal	volts	20000.0	1.9499999999999999e-07
+19	19	neural signal	volts	20000.0	1.9499999999999999e-07
+20	20	neural signal	volts	20000.0	1.9499999999999999e-07
+21	21	neural signal	volts	20000.0	1.9499999999999999e-07
+22	22	neural signal	volts	20000.0	1.9499999999999999e-07
+23	23	neural signal	volts	20000.0	1.9499999999999999e-07
+24	24	neural signal	volts	20000.0	1.9499999999999999e-07
+25	25	neural signal	volts	20000.0	1.9499999999999999e-07
+26	26	neural signal	volts	20000.0	1.9499999999999999e-07
+27	27	neural signal	volts	20000.0	1.9499999999999999e-07
+28	28	neural signal	volts	20000.0	1.9499999999999999e-07
+29	29	neural signal	volts	20000.0	1.9499999999999999e-07
+30	30	neural signal	volts	20000.0	1.9499999999999999e-07
+31	31	neural signal	volts	20000.0	1.9499999999999999e-07
+32	32	neural signal	volts	20000.0	1.9499999999999999e-07
+33	33	neural signal	volts	20000.0	1.9499999999999999e-07
+34	34	neural signal	volts	20000.0	1.9499999999999999e-07
+35	35	neural signal	volts	20000.0	1.9499999999999999e-07
+36	36	neural signal	volts	20000.0	1.9499999999999999e-07
+37	37	neural signal	volts	20000.0	1.9499999999999999e-07
+38	38	neural signal	volts	20000.0	1.9499999999999999e-07
+39	39	neural signal	volts	20000.0	1.9499999999999999e-07
+40	40	neural signal	volts	20000.0	1.9499999999999999e-07
+41	41	neural signal	volts	20000.0	1.9499999999999999e-07
+42	42	neural signal	volts	20000.0	1.9499999999999999e-07
+43	43	neural signal	volts	20000.0	1.9499999999999999e-07
+44	44	neural signal	volts	20000.0	1.9499999999999999e-07
+45	45	neural signal	volts	20000.0	1.9499999999999999e-07
+46	46	neural signal	volts	20000.0	1.9499999999999999e-07
+47	47	neural signal	volts	20000.0	1.9499999999999999e-07
+48	48	neural signal	volts	20000.0	1.9499999999999999e-07
+49	49	neural signal	volts	20000.0	1.9499999999999999e-07
+50	50	neural signal	volts	20000.0	1.9499999999999999e-07
+51	51	neural signal	volts	20000.0	1.9499999999999999e-07
+52	52	neural signal	volts	20000.0	1.9499999999999999e-07
+53	53	neural signal	volts	20000.0	1.9499999999999999e-07
+54	54	neural signal	volts	20000.0	1.9499999999999999e-07
+55	55	neural signal	volts	20000.0	1.9499999999999999e-07
+56	56	neural signal	volts	20000.0	1.9499999999999999e-07
+57	57	neural signal	volts	20000.0	1.9499999999999999e-07
+58	58	neural signal	volts	20000.0	1.9499999999999999e-07
+59	59	neural signal	volts	20000.0	1.9499999999999999e-07
+60	60	neural signal	volts	20000.0	1.9499999999999999e-07
+61	61	neural signal	volts	20000.0	1.9499999999999999e-07
+62	62	neural signal	volts	20000.0	1.9499999999999999e-07
+63	63	neural signal	volts	20000.0	1.9499999999999999e-07
+64	64	neural signal	volts	20000.0	1.9499999999999999e-07
+65	65	neural signal	volts	20000.0	1.9499999999999999e-07
+66	66	neural signal	volts	20000.0	1.9499999999999999e-07
+67	67	neural signal	volts	20000.0	1.9499999999999999e-07
+68	68	neural signal	volts	20000.0	1.9499999999999999e-07
+69	69	neural signal	volts	20000.0	1.9499999999999999e-07
+70	70	neural signal	volts	20000.0	1.9499999999999999e-07
+71	71	neural signal	volts	20000.0	1.9499999999999999e-07
+72	72	neural signal	volts	20000.0	1.9499999999999999e-07
+73	73	neural signal	volts	20000.0	1.9499999999999999e-07
+74	74	neural signal	volts	20000.0	1.9499999999999999e-07
+75	75	neural signal	volts	20000.0	1.9499999999999999e-07
+76	76	neural signal	volts	20000.0	1.9499999999999999e-07
+77	77	neural signal	volts	20000.0	1.9499999999999999e-07
+78	78	neural signal	volts	20000.0	1.9499999999999999e-07
+79	79	neural signal	volts	20000.0	1.9499999999999999e-07
+80	80	neural signal	volts	20000.0	1.9499999999999999e-07
+81	81	neural signal	volts	20000.0	1.9499999999999999e-07
+82	82	neural signal	volts	20000.0	1.9499999999999999e-07
+83	83	neural signal	volts	20000.0	1.9499999999999999e-07
+84	84	neural signal	volts	20000.0	1.9499999999999999e-07
+85	85	neural signal	volts	20000.0	1.9499999999999999e-07
+86	86	neural signal	volts	20000.0	1.9499999999999999e-07
+87	87	neural signal	volts	20000.0	1.9499999999999999e-07
+88	88	neural signal	volts	20000.0	1.9499999999999999e-07
+89	89	neural signal	volts	20000.0	1.9499999999999999e-07
+90	90	neural signal	volts	20000.0	1.9499999999999999e-07
+91	91	neural signal	volts	20000.0	1.9499999999999999e-07
+92	92	neural signal	volts	20000.0	1.9499999999999999e-07
+93	93	neural signal	volts	20000.0	1.9499999999999999e-07
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+95	95	neural signal	volts	20000.0	1.9499999999999999e-07
+96	96	neural signal	volts	20000.0	1.9499999999999999e-07
+97	97	neural signal	volts	20000.0	1.9499999999999999e-07
+98	98	neural signal	volts	20000.0	1.9499999999999999e-07
+99	99	neural signal	volts	20000.0	1.9499999999999999e-07
+100	100	neural signal	volts	20000.0	1.9499999999999999e-07
+101	101	neural signal	volts	20000.0	1.9499999999999999e-07
+102	102	neural signal	volts	20000.0	1.9499999999999999e-07
+103	103	neural signal	volts	20000.0	1.9499999999999999e-07
+104	104	neural signal	volts	20000.0	1.9499999999999999e-07
+105	105	neural signal	volts	20000.0	1.9499999999999999e-07
+106	106	neural signal	volts	20000.0	1.9499999999999999e-07
+107	107	neural signal	volts	20000.0	1.9499999999999999e-07
+108	108	neural signal	volts	20000.0	1.9499999999999999e-07
+109	109	neural signal	volts	20000.0	1.9499999999999999e-07
+110	110	neural signal	volts	20000.0	1.9499999999999999e-07
+111	111	neural signal	volts	20000.0	1.9499999999999999e-07
+112	112	neural signal	volts	20000.0	1.9499999999999999e-07
+113	113	neural signal	volts	20000.0	1.9499999999999999e-07
+114	114	neural signal	volts	20000.0	1.9499999999999999e-07
+115	115	neural signal	volts	20000.0	1.9499999999999999e-07
+116	116	neural signal	volts	20000.0	1.9499999999999999e-07
+117	117	neural signal	volts	20000.0	1.9499999999999999e-07
+118	118	neural signal	volts	20000.0	1.9499999999999999e-07
+119	119	neural signal	volts	20000.0	1.9499999999999999e-07
+120	120	neural signal	volts	20000.0	1.9499999999999999e-07
+121	121	neural signal	volts	20000.0	1.9499999999999999e-07
+122	122	neural signal	volts	20000.0	1.9499999999999999e-07
+123	123	neural signal	volts	20000.0	1.9499999999999999e-07
+124	124	neural signal	volts	20000.0	1.9499999999999999e-07
+125	125	neural signal	volts	20000.0	1.9499999999999999e-07
+126	126	neural signal	volts	20000.0	1.9499999999999999e-07
+127	127	neural signal	volts	20000.0	1.9499999999999999e-07

+ 129 - 0
ephys_nwb_petersen/sub-MS12/ses-PeterMS12170718101720concat/ephys/sub-MS12_ses-PeterMS12170718101720concat_contacts.tsv

@@ -0,0 +1,129 @@
+impedance	contact_id	probe_id	Location
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+-1.0	1	Device	unknown
+-1.0	2	Device	unknown
+-1.0	3	Device	unknown
+-1.0	4	Device	unknown
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+-1.0	6	Device	unknown
+-1.0	7	Device	unknown
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+-1.0	9	Device	unknown
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+-1.0	14	Device	unknown
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+-1.0	25	Device	unknown
+-1.0	26	Device	unknown
+-1.0	27	Device	unknown
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ephys_nwb_petersen/sub-MS12/ses-PeterMS12170718101720concat/ephys/sub-MS12_ses-PeterMS12170718101720concat_ephys.json

@@ -0,0 +1 @@
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ephys_nwb_petersen/sub-MS12/ses-PeterMS12170718101720concat/ephys/sub-MS12_ses-PeterMS12170718101720concat_ephys.nwb

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ephys_nwb_petersen/sub-MS12/ses-PeterMS12170718101720concat/ephys/sub-MS12_ses-PeterMS12170718101720concat_probes.tsv

@@ -0,0 +1,2 @@
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ephys_nwb_petersen/sub-MS12/ses-PeterMS12170719095305concat/ephys/sub-MS12_ses-PeterMS12170719095305concat_channels.tsv

@@ -0,0 +1,129 @@
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ephys_nwb_petersen/sub-MS12/ses-PeterMS12170719095305concat/ephys/sub-MS12_ses-PeterMS12170719095305concat_contacts.tsv

@@ -0,0 +1,129 @@
+impedance	contact_id	probe_id	Location
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ephys_nwb_petersen/sub-MS12/ses-PeterMS12170719095305concat/ephys/sub-MS12_ses-PeterMS12170719095305concat_ephys.json

@@ -0,0 +1 @@
+{"PowerLineFrequency": 60.0}

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ephys_nwb_petersen/sub-MS12/ses-PeterMS12170719095305concat/ephys/sub-MS12_ses-PeterMS12170719095305concat_ephys.nwb

@@ -0,0 +1 @@
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ephys_nwb_petersen/sub-MS12/ses-PeterMS12170719095305concat/ephys/sub-MS12_ses-PeterMS12170719095305concat_probes.tsv

@@ -0,0 +1,2 @@
+probeID	type
+Device	acute

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ephys_nwb_petersen/sub-MS12/ses-PeterMS12170720093528concat/ephys/sub-MS12_ses-PeterMS12170720093528concat_channels.tsv

@@ -0,0 +1,129 @@
+channel_id	Contact_id	type	units	sampling_frequency	unit_conversion_multiplier
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ephys_nwb_petersen/sub-MS12/ses-PeterMS12170720093528concat/ephys/sub-MS12_ses-PeterMS12170720093528concat_contacts.tsv

@@ -0,0 +1,129 @@
+impedance	contact_id	probe_id	Location
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ephys_nwb_petersen/sub-MS12/ses-PeterMS12170720093528concat/ephys/sub-MS12_ses-PeterMS12170720093528concat_ephys.json

@@ -0,0 +1 @@
+{"PowerLineFrequency": 60.0}

+ 1 - 0
ephys_nwb_petersen/sub-MS12/ses-PeterMS12170720093528concat/ephys/sub-MS12_ses-PeterMS12170720093528concat_ephys.nwb

@@ -0,0 +1 @@
+/annex/objects/MD5-s252184--c6cbc388bbc4edd2e89a7ece674f254a

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ephys_nwb_petersen/sub-MS12/ses-PeterMS12170720093528concat/ephys/sub-MS12_ses-PeterMS12170720093528concat_probes.tsv

@@ -0,0 +1,2 @@
+probeID	type
+Device	acute

+ 129 - 0
ephys_nwb_petersen/sub-MS12/ses-PeterMS12170723141121concat/ephys/sub-MS12_ses-PeterMS12170723141121concat_channels.tsv

@@ -0,0 +1,129 @@
+channel_id	Contact_id	type	units	sampling_frequency	unit_conversion_multiplier
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+1	1	neural signal	volts	20000.0	1.9499999999999999e-07
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+4	4	neural signal	volts	20000.0	1.9499999999999999e-07
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+6	6	neural signal	volts	20000.0	1.9499999999999999e-07
+7	7	neural signal	volts	20000.0	1.9499999999999999e-07
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+9	9	neural signal	volts	20000.0	1.9499999999999999e-07
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+11	11	neural signal	volts	20000.0	1.9499999999999999e-07
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+28	28	neural signal	volts	20000.0	1.9499999999999999e-07
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+34	34	neural signal	volts	20000.0	1.9499999999999999e-07
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+41	41	neural signal	volts	20000.0	1.9499999999999999e-07
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+111	111	neural signal	volts	20000.0	1.9499999999999999e-07
+112	112	neural signal	volts	20000.0	1.9499999999999999e-07
+113	113	neural signal	volts	20000.0	1.9499999999999999e-07
+114	114	neural signal	volts	20000.0	1.9499999999999999e-07
+115	115	neural signal	volts	20000.0	1.9499999999999999e-07
+116	116	neural signal	volts	20000.0	1.9499999999999999e-07
+117	117	neural signal	volts	20000.0	1.9499999999999999e-07
+118	118	neural signal	volts	20000.0	1.9499999999999999e-07
+119	119	neural signal	volts	20000.0	1.9499999999999999e-07
+120	120	neural signal	volts	20000.0	1.9499999999999999e-07
+121	121	neural signal	volts	20000.0	1.9499999999999999e-07
+122	122	neural signal	volts	20000.0	1.9499999999999999e-07
+123	123	neural signal	volts	20000.0	1.9499999999999999e-07
+124	124	neural signal	volts	20000.0	1.9499999999999999e-07
+125	125	neural signal	volts	20000.0	1.9499999999999999e-07
+126	126	neural signal	volts	20000.0	1.9499999999999999e-07
+127	127	neural signal	volts	20000.0	1.9499999999999999e-07

+ 129 - 0
ephys_nwb_petersen/sub-MS12/ses-PeterMS12170723141121concat/ephys/sub-MS12_ses-PeterMS12170723141121concat_contacts.tsv

@@ -0,0 +1,129 @@
+impedance	contact_id	probe_id	Location
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+-1.0	1	Device	unknown
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+-1.0	3	Device	unknown
+-1.0	4	Device	unknown
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ephys_nwb_petersen/sub-MS12/ses-PeterMS12170723141121concat/ephys/sub-MS12_ses-PeterMS12170723141121concat_ephys.json

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ephys_nwb_petersen/sub-MS12/ses-PeterMS12170723141121concat/ephys/sub-MS12_ses-PeterMS12170723141121concat_ephys.nwb

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ephys_nwb_petersen/sub-MS12/ses-PeterMS12170723141121concat/ephys/sub-MS12_ses-PeterMS12170723141121concat_probes.tsv

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+ses-PeterMS12170712101120concat	96.0	Petersen et al. demonstrate that cooling of the medial septum slows theta oscillation and increases choice errors without affecting spatial features of pyramidal neurons. Cooling affects distance-time, but not distance-theta phase, compression. The findings reveal that cell assemblies are organized by theta phase and not by external (clock) time.
+ses-PeterMS12170713093400concat	115.0	Petersen et al. demonstrate that cooling of the medial septum slows theta oscillation and increases choice errors without affecting spatial features of pyramidal neurons. Cooling affects distance-time, but not distance-theta phase, compression. The findings reveal that cell assemblies are organized by theta phase and not by external (clock) time.
+ses-PeterMS12170714122034concat	151.0	Petersen et al. demonstrate that cooling of the medial septum slows theta oscillation and increases choice errors without affecting spatial features of pyramidal neurons. Cooling affects distance-time, but not distance-theta phase, compression. The findings reveal that cell assemblies are organized by theta phase and not by external (clock) time.
+ses-PeterMS12170716172307concat	146.0	Petersen et al. demonstrate that cooling of the medial septum slows theta oscillation and increases choice errors without affecting spatial features of pyramidal neurons. Cooling affects distance-time, but not distance-theta phase, compression. The findings reveal that cell assemblies are organized by theta phase and not by external (clock) time.
+ses-PeterMS12170717111614concat	134.0	Petersen et al. demonstrate that cooling of the medial septum slows theta oscillation and increases choice errors without affecting spatial features of pyramidal neurons. Cooling affects distance-time, but not distance-theta phase, compression. The findings reveal that cell assemblies are organized by theta phase and not by external (clock) time.
+ses-PeterMS12170718101720concat	125.0	Petersen et al. demonstrate that cooling of the medial septum slows theta oscillation and increases choice errors without affecting spatial features of pyramidal neurons. Cooling affects distance-time, but not distance-theta phase, compression. The findings reveal that cell assemblies are organized by theta phase and not by external (clock) time.
+ses-PeterMS12170719095305concat		Petersen et al. demonstrate that cooling of the medial septum slows theta oscillation and increases choice errors without affecting spatial features of pyramidal neurons. Cooling affects distance-time, but not distance-theta phase, compression. The findings reveal that cell assemblies are organized by theta phase and not by external (clock) time.
+ses-PeterMS12170720093528concat	155.0	Petersen et al. demonstrate that cooling of the medial septum slows theta oscillation and increases choice errors without affecting spatial features of pyramidal neurons. Cooling affects distance-time, but not distance-theta phase, compression. The findings reveal that cell assemblies are organized by theta phase and not by external (clock) time.
+ses-PeterMS12170723141121concat	140.0	Petersen et al. demonstrate that cooling of the medial septum slows theta oscillation and increases choice errors without affecting spatial features of pyramidal neurons. Cooling affects distance-time, but not distance-theta phase, compression. The findings reveal that cell assemblies are organized by theta phase and not by external (clock) time.

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ephys_nwb_petersen/sub-MS13/ses-PeterMS13171127133330concat/ephys/sub-MS13_ses-PeterMS13171127133330concat_channels.tsv

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ephys_nwb_petersen/sub-MS13/ses-PeterMS13171127133330concat/ephys/sub-MS13_ses-PeterMS13171127133330concat_ephys.json

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ephys_nwb_petersen/sub-MS13/ses-PeterMS13171127133330concat/ephys/sub-MS13_ses-PeterMS13171127133330concat_ephys.nwb

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ephys_nwb_petersen/sub-MS13/ses-PeterMS13171128113924concat/ephys/sub-MS13_ses-PeterMS13171128113924concat_contacts.tsv

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ephys_nwb_petersen/sub-MS13/ses-PeterMS13171128113924concat/ephys/sub-MS13_ses-PeterMS13171128113924concat_ephys.json


이 변경점에서 너무 많은 파일들이 변경되어 몇몇 파일들은 표시되지 않았습니다.