covariance nmr toolbox (matlab platform) Search Results


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Mean transverse relaxation times (a) and their representative apparent water populations (b) of cocoyam roots as a function of cooking temperature (n = 10 for each variety). The T2 relaxation times were estimated by <t>discrete</t> <t>exponential</t> fitting of <t>LF-NMR</t> CPMG relaxation curves of the test samples at each temperature
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fmri toolbox  (MathWorks Inc)
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Mean transverse relaxation times (a) and their representative apparent water populations (b) of cocoyam roots as a function of cooking temperature (n = 10 for each variety). The T2 relaxation times were estimated by <t>discrete</t> <t>exponential</t> fitting of <t>LF-NMR</t> CPMG relaxation curves of the test samples at each temperature
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covariates  (MathWorks Inc)
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Mean transverse relaxation times (a) and their representative apparent water populations (b) of cocoyam roots as a function of cooking temperature (n = 10 for each variety). The T2 relaxation times were estimated by <t>discrete</t> <t>exponential</t> fitting of <t>LF-NMR</t> CPMG relaxation curves of the test samples at each temperature
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(A) The within‐network reliability analysis across three experimental trials (Trials 1, 2, and 3: <t>BOLD‐fMRI</t> scan at Days 0–1, Days 2–3, and Days 4–5, respectively) was assessed by the MN sub‐networks in the sham control group. No significant difference was observed in any sub‐networks. (B). The within‐network reliability across three trials was assessed by the MN sub‐networks in the KA group. A significantly large ICA intensity was observed in Trial 2 vs. Trial 1 in the PrR, Trial 2 vs. Trial 1 in the DHpL, and Trial 3 vs. Trial 2 in the DHpR. One asterisk (*) identifies adjusted P values lower than 0.1. (C). Intraclass correlation coefficient (ICC) reflects the test–retest reliability in four MN sub‐networks in the sham rats and KA rats. It indicated a low‐to‐excellent reliability in sham, while the average reliability dropped in the KA group.
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(A) The within‐network reliability analysis across three experimental trials (Trials 1, 2, and 3: <t>BOLD‐fMRI</t> scan at Days 0–1, Days 2–3, and Days 4–5, respectively) was assessed by the MN sub‐networks in the sham control group. No significant difference was observed in any sub‐networks. (B). The within‐network reliability across three trials was assessed by the MN sub‐networks in the KA group. A significantly large ICA intensity was observed in Trial 2 vs. Trial 1 in the PrR, Trial 2 vs. Trial 1 in the DHpL, and Trial 3 vs. Trial 2 in the DHpR. One asterisk (*) identifies adjusted P values lower than 0.1. (C). Intraclass correlation coefficient (ICC) reflects the test–retest reliability in four MN sub‐networks in the sham rats and KA rats. It indicated a low‐to‐excellent reliability in sham, while the average reliability dropped in the KA group.
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(A) The within‐network reliability analysis across three experimental trials (Trials 1, 2, and 3: <t>BOLD‐fMRI</t> scan at Days 0–1, Days 2–3, and Days 4–5, respectively) was assessed by the MN sub‐networks in the sham control group. No significant difference was observed in any sub‐networks. (B). The within‐network reliability across three trials was assessed by the MN sub‐networks in the KA group. A significantly large ICA intensity was observed in Trial 2 vs. Trial 1 in the PrR, Trial 2 vs. Trial 1 in the DHpL, and Trial 3 vs. Trial 2 in the DHpR. One asterisk (*) identifies adjusted P values lower than 0.1. (C). Intraclass correlation coefficient (ICC) reflects the test–retest reliability in four MN sub‐networks in the sham rats and KA rats. It indicated a low‐to‐excellent reliability in sham, while the average reliability dropped in the KA group.
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(A) The within‐network reliability analysis across three experimental trials (Trials 1, 2, and 3: <t>BOLD‐fMRI</t> scan at Days 0–1, Days 2–3, and Days 4–5, respectively) was assessed by the MN sub‐networks in the sham control group. No significant difference was observed in any sub‐networks. (B). The within‐network reliability across three trials was assessed by the MN sub‐networks in the KA group. A significantly large ICA intensity was observed in Trial 2 vs. Trial 1 in the PrR, Trial 2 vs. Trial 1 in the DHpL, and Trial 3 vs. Trial 2 in the DHpR. One asterisk (*) identifies adjusted P values lower than 0.1. (C). Intraclass correlation coefficient (ICC) reflects the test–retest reliability in four MN sub‐networks in the sham rats and KA rats. It indicated a low‐to‐excellent reliability in sham, while the average reliability dropped in the KA group.
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in house scripts on matlab7  (MathWorks Inc)
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(A) The within‐network reliability analysis across three experimental trials (Trials 1, 2, and 3: <t>BOLD‐fMRI</t> scan at Days 0–1, Days 2–3, and Days 4–5, respectively) was assessed by the MN sub‐networks in the sham control group. No significant difference was observed in any sub‐networks. (B). The within‐network reliability across three trials was assessed by the MN sub‐networks in the KA group. A significantly large ICA intensity was observed in Trial 2 vs. Trial 1 in the PrR, Trial 2 vs. Trial 1 in the DHpL, and Trial 3 vs. Trial 2 in the DHpR. One asterisk (*) identifies adjusted P values lower than 0.1. (C). Intraclass correlation coefficient (ICC) reflects the test–retest reliability in four MN sub‐networks in the sham rats and KA rats. It indicated a low‐to‐excellent reliability in sham, while the average reliability dropped in the KA group.
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(A) The within‐network reliability analysis across three experimental trials (Trials 1, 2, and 3: <t>BOLD‐fMRI</t> scan at Days 0–1, Days 2–3, and Days 4–5, respectively) was assessed by the MN sub‐networks in the sham control group. No significant difference was observed in any sub‐networks. (B). The within‐network reliability across three trials was assessed by the MN sub‐networks in the KA group. A significantly large ICA intensity was observed in Trial 2 vs. Trial 1 in the PrR, Trial 2 vs. Trial 1 in the DHpL, and Trial 3 vs. Trial 2 in the DHpR. One asterisk (*) identifies adjusted P values lower than 0.1. (C). Intraclass correlation coefficient (ICC) reflects the test–retest reliability in four MN sub‐networks in the sham rats and KA rats. It indicated a low‐to‐excellent reliability in sham, while the average reliability dropped in the KA group.
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Image Search Results


Mean transverse relaxation times (a) and their representative apparent water populations (b) of cocoyam roots as a function of cooking temperature (n = 10 for each variety). The T2 relaxation times were estimated by discrete exponential fitting of LF-NMR CPMG relaxation curves of the test samples at each temperature

Journal: Journal of Food Science and Technology

Article Title: Characteristics of Xanthosoma sagittifolium roots during cooking, using physicochemical analysis, uniaxial compression, multispectral imaging and low field NMR spectroscopy

doi: 10.1007/s13197-017-2704-7

Figure Lengend Snippet: Mean transverse relaxation times (a) and their representative apparent water populations (b) of cocoyam roots as a function of cooking temperature (n = 10 for each variety). The T2 relaxation times were estimated by discrete exponential fitting of LF-NMR CPMG relaxation curves of the test samples at each temperature

Article Snippet: Eight repetitive scans were used for data fitting and the repetition time between scans was set to 6 s. The Low-Field NMR Toolbox for Matlab (The Matworks Inc., Natric MA, USA) was then used for multi-exponential fitting of the data, as described by Pedersen et al. ( 2002 ).

Techniques:

(A) The within‐network reliability analysis across three experimental trials (Trials 1, 2, and 3: BOLD‐fMRI scan at Days 0–1, Days 2–3, and Days 4–5, respectively) was assessed by the MN sub‐networks in the sham control group. No significant difference was observed in any sub‐networks. (B). The within‐network reliability across three trials was assessed by the MN sub‐networks in the KA group. A significantly large ICA intensity was observed in Trial 2 vs. Trial 1 in the PrR, Trial 2 vs. Trial 1 in the DHpL, and Trial 3 vs. Trial 2 in the DHpR. One asterisk (*) identifies adjusted P values lower than 0.1. (C). Intraclass correlation coefficient (ICC) reflects the test–retest reliability in four MN sub‐networks in the sham rats and KA rats. It indicated a low‐to‐excellent reliability in sham, while the average reliability dropped in the KA group.

Journal: Epilepsia Open

Article Title: Intrinsic brain network stability during kainic acid‐induced epileptogenesis

doi: 10.1002/epi4.70002

Figure Lengend Snippet: (A) The within‐network reliability analysis across three experimental trials (Trials 1, 2, and 3: BOLD‐fMRI scan at Days 0–1, Days 2–3, and Days 4–5, respectively) was assessed by the MN sub‐networks in the sham control group. No significant difference was observed in any sub‐networks. (B). The within‐network reliability across three trials was assessed by the MN sub‐networks in the KA group. A significantly large ICA intensity was observed in Trial 2 vs. Trial 1 in the PrR, Trial 2 vs. Trial 1 in the DHpL, and Trial 3 vs. Trial 2 in the DHpR. One asterisk (*) identifies adjusted P values lower than 0.1. (C). Intraclass correlation coefficient (ICC) reflects the test–retest reliability in four MN sub‐networks in the sham rats and KA rats. It indicated a low‐to‐excellent reliability in sham, while the average reliability dropped in the KA group.

Article Snippet: Group‐level BOLD‐fMRI data were analyzed using GICA in the Group ICA of FMRI Toolbox (GIFT) Matlab software to identify MNs during brain resting state.

Techniques: Control