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matlab function mafdr  (MathWorks Inc)


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    MathWorks Inc matlab function mafdr
    Matlab Function Mafdr, supplied by MathWorks Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/matlab+mafdr+function/pm39988134-90-7-7
    Average 90 stars, based on 1 article reviews
    matlab function mafdr - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    Generated:

    Article Title: When the Whole Is Less Than the Sum of Its Parts: Maximum Object Category Information and Behavioral Prediction in Multiscale Activation Patterns
    Article Snippet: .. The correlation was considered significant if surpassed 95% of the randomly generated correlations in the null distribution in either positive or negative directions ( p < 0.05) and the p -values were corrected for multiple comparisons across time using Matlab mafdr function, where the algorithm fixes the rejection region and then estimates its corresponding error rate resulting in increased accuracy and power ( ). ..

    other:

    Article Title: Exploratory analysis of the relationship between striatal connectivity and apathy during phosphodiesterase 10 inhibition in schizophrenia: findings from a randomized crossover trial.
    Article Snippet: For all analyses with multiple comparisons, p values were corrected according to the Benjamini–Hochberg procedure as implemented in the Matlab mafdr-function.

    Article Title: Characterizing Relevant MicroRNA Editing Sites in Parkinson's Disease.
    Article Snippet: The obtained p-values were corrected using the Benjamini and Horchberg method [40] using the mafdr function in MatLab (Mathworks, MA, USA).

    Article Title: Characterizing Relevant MicroRNA Editing Sites in Parkinson’s Disease
    Article Snippet: The obtained p -values were corrected using the Benjamini and Horchberg method [ ] using the mafdr function in MatLab (Mathworks, MA, USA).

    Article Title: Temporal dynamic changes of intrinsic brain regional activity in depression with smoking.
    Article Snippet: Background: Depression is often accompanied by high levels of smoking behavior, and smoking can act as a risk factor for depression.. However, there is limited neuroimaging evidence regarding the association between depression and smoking, especially the impact of this association on the brain stability remains unclear.. Therefore, this study aimed to assess the interaction effect between smoking and depression from a neurodynamic perspective.

    Article Title: Distinct factors associated with short-term and long-term weight loss induced by low-fat or low-carbohydrate diet intervention
    Article Snippet: Matlab function mafdr , MathWorks , https://www.mathworks.com/help/bioinfo/ref/mafdr.html?s_tid=doc_ta.



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    ( A ), ( B ) Histograms of waveform widths for recorded neurons in CFA ( A ) and RFA ( B ), showing the bimodal distribution of narrow and wide waveforms. Dotted line shows the threshold above which neurons were considered wide waveform. ( C )-( F ) Histograms of p-values from our modified version of SALT for narrow-waveform neurons recorded in one session ( C,E ) or all sessions ( D,F ) in either CFA ( C,D ) or RFA ( E,F ) while inactivating the other region. The uniformity of these distributions indicates an absence of appreciable violation of the null <t>hypotheses</t> that neurons are not directly activated by light. ( G )-( N ) Mean firing rate ± SEM for wide-waveform ( G–J ) or narrow-waveform ( K–N ) neurons for one animal ( G,I,K,M ) or three animals ( H,J,L,N ) recorded in CFA ( G,H,K,L ) or RFA ( I,J,M,N ) while inactivating the other region. Averages combining cells from multiple animals used the same number of cells from each animal. The cyan rectangle indicates when the light was applied. ( O )-( R ) Mean absolute firing rate change ± SEM between control and inactivation trials ( O,Q ) and mean absolute firing rate difference between control and inactivation trials averaged from 10ms after light/trial onset to 25, 50, or 100ms afterwards ( P,R ) for wide- and narrow-waveform neurons recorded in CFA ( O,P ) or RFA ( Q,R ) during inactivation of the other region. Black bars show mean across animals. ( T )-(AA) Mean firing rate ± SEM for all three animals recorded in CFA ( T,U,X,Y ) or RFA ( V,W,Z,AA ) while inactivating the other region, either for two separate sessions ( T–W ) or the first and second half of trials from all sessions ( X–AA ). The cyan rectangle indicates when the light was applied. Average inactivation effects show remarkable consistency, both within and across sessions.
    Matlab Function 'Mafdr, supplied by MathWorks Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    matlab function mafdr  (MathWorks Inc)
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    ( A ), ( B ) Histograms of waveform widths for recorded neurons in CFA ( A ) and RFA ( B ), showing the bimodal distribution of narrow and wide waveforms. Dotted line shows the threshold above which neurons were considered wide waveform. ( C )-( F ) Histograms of p-values from our modified version of SALT for narrow-waveform neurons recorded in one session ( C,E ) or all sessions ( D,F ) in either CFA ( C,D ) or RFA ( E,F ) while inactivating the other region. The uniformity of these distributions indicates an absence of appreciable violation of the null <t>hypotheses</t> that neurons are not directly activated by light. ( G )-( N ) Mean firing rate ± SEM for wide-waveform ( G–J ) or narrow-waveform ( K–N ) neurons for one animal ( G,I,K,M ) or three animals ( H,J,L,N ) recorded in CFA ( G,H,K,L ) or RFA ( I,J,M,N ) while inactivating the other region. Averages combining cells from multiple animals used the same number of cells from each animal. The cyan rectangle indicates when the light was applied. ( O )-( R ) Mean absolute firing rate change ± SEM between control and inactivation trials ( O,Q ) and mean absolute firing rate difference between control and inactivation trials averaged from 10ms after light/trial onset to 25, 50, or 100ms afterwards ( P,R ) for wide- and narrow-waveform neurons recorded in CFA ( O,P ) or RFA ( Q,R ) during inactivation of the other region. Black bars show mean across animals. ( T )-(AA) Mean firing rate ± SEM for all three animals recorded in CFA ( T,U,X,Y ) or RFA ( V,W,Z,AA ) while inactivating the other region, either for two separate sessions ( T–W ) or the first and second half of trials from all sessions ( X–AA ). The cyan rectangle indicates when the light was applied. Average inactivation effects show remarkable consistency, both within and across sessions.
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    matlab mafdr-function  (MathWorks Inc)
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    ( A ), ( B ) Histograms of waveform widths for recorded neurons in CFA ( A ) and RFA ( B ), showing the bimodal distribution of narrow and wide waveforms. Dotted line shows the threshold above which neurons were considered wide waveform. ( C )-( F ) Histograms of p-values from our modified version of SALT for narrow-waveform neurons recorded in one session ( C,E ) or all sessions ( D,F ) in either CFA ( C,D ) or RFA ( E,F ) while inactivating the other region. The uniformity of these distributions indicates an absence of appreciable violation of the null <t>hypotheses</t> that neurons are not directly activated by light. ( G )-( N ) Mean firing rate ± SEM for wide-waveform ( G–J ) or narrow-waveform ( K–N ) neurons for one animal ( G,I,K,M ) or three animals ( H,J,L,N ) recorded in CFA ( G,H,K,L ) or RFA ( I,J,M,N ) while inactivating the other region. Averages combining cells from multiple animals used the same number of cells from each animal. The cyan rectangle indicates when the light was applied. ( O )-( R ) Mean absolute firing rate change ± SEM between control and inactivation trials ( O,Q ) and mean absolute firing rate difference between control and inactivation trials averaged from 10ms after light/trial onset to 25, 50, or 100ms afterwards ( P,R ) for wide- and narrow-waveform neurons recorded in CFA ( O,P ) or RFA ( Q,R ) during inactivation of the other region. Black bars show mean across animals. ( T )-(AA) Mean firing rate ± SEM for all three animals recorded in CFA ( T,U,X,Y ) or RFA ( V,W,Z,AA ) while inactivating the other region, either for two separate sessions ( T–W ) or the first and second half of trials from all sessions ( X–AA ). The cyan rectangle indicates when the light was applied. Average inactivation effects show remarkable consistency, both within and across sessions.
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    ( A ), ( B ) Histograms of waveform widths for recorded neurons in CFA ( A ) and RFA ( B ), showing the bimodal distribution of narrow and wide waveforms. Dotted line shows the threshold above which neurons were considered wide waveform. ( C )-( F ) Histograms of p-values from our modified version of SALT for narrow-waveform neurons recorded in one session ( C,E ) or all sessions ( D,F ) in either CFA ( C,D ) or RFA ( E,F ) while inactivating the other region. The uniformity of these distributions indicates an absence of appreciable violation of the null <t>hypotheses</t> that neurons are not directly activated by light. ( G )-( N ) Mean firing rate ± SEM for wide-waveform ( G–J ) or narrow-waveform ( K–N ) neurons for one animal ( G,I,K,M ) or three animals ( H,J,L,N ) recorded in CFA ( G,H,K,L ) or RFA ( I,J,M,N ) while inactivating the other region. Averages combining cells from multiple animals used the same number of cells from each animal. The cyan rectangle indicates when the light was applied. ( O )-( R ) Mean absolute firing rate change ± SEM between control and inactivation trials ( O,Q ) and mean absolute firing rate difference between control and inactivation trials averaged from 10ms after light/trial onset to 25, 50, or 100ms afterwards ( P,R ) for wide- and narrow-waveform neurons recorded in CFA ( O,P ) or RFA ( Q,R ) during inactivation of the other region. Black bars show mean across animals. ( T )-(AA) Mean firing rate ± SEM for all three animals recorded in CFA ( T,U,X,Y ) or RFA ( V,W,Z,AA ) while inactivating the other region, either for two separate sessions ( T–W ) or the first and second half of trials from all sessions ( X–AA ). The cyan rectangle indicates when the light was applied. Average inactivation effects show remarkable consistency, both within and across sessions.
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    matlab mafdr function  (MathWorks Inc)
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    ( A ), ( B ) Histograms of waveform widths for recorded neurons in CFA ( A ) and RFA ( B ), showing the bimodal distribution of narrow and wide waveforms. Dotted line shows the threshold above which neurons were considered wide waveform. ( C )-( F ) Histograms of p-values from our modified version of SALT for narrow-waveform neurons recorded in one session ( C,E ) or all sessions ( D,F ) in either CFA ( C,D ) or RFA ( E,F ) while inactivating the other region. The uniformity of these distributions indicates an absence of appreciable violation of the null <t>hypotheses</t> that neurons are not directly activated by light. ( G )-( N ) Mean firing rate ± SEM for wide-waveform ( G–J ) or narrow-waveform ( K–N ) neurons for one animal ( G,I,K,M ) or three animals ( H,J,L,N ) recorded in CFA ( G,H,K,L ) or RFA ( I,J,M,N ) while inactivating the other region. Averages combining cells from multiple animals used the same number of cells from each animal. The cyan rectangle indicates when the light was applied. ( O )-( R ) Mean absolute firing rate change ± SEM between control and inactivation trials ( O,Q ) and mean absolute firing rate difference between control and inactivation trials averaged from 10ms after light/trial onset to 25, 50, or 100ms afterwards ( P,R ) for wide- and narrow-waveform neurons recorded in CFA ( O,P ) or RFA ( Q,R ) during inactivation of the other region. Black bars show mean across animals. ( T )-(AA) Mean firing rate ± SEM for all three animals recorded in CFA ( T,U,X,Y ) or RFA ( V,W,Z,AA ) while inactivating the other region, either for two separate sessions ( T–W ) or the first and second half of trials from all sessions ( X–AA ). The cyan rectangle indicates when the light was applied. Average inactivation effects show remarkable consistency, both within and across sessions.
    Matlab Mafdr Function, supplied by MathWorks Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/matlab+mafdr+function/10__1158_slash_2767___9764__crc___23___0330-54-25-24
    Average 90 stars, based on 1 article reviews
    matlab mafdr function - by Bioz Stars, 2026-09
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    Image Search Results


    ( A ), ( B ) Histograms of waveform widths for recorded neurons in CFA ( A ) and RFA ( B ), showing the bimodal distribution of narrow and wide waveforms. Dotted line shows the threshold above which neurons were considered wide waveform. ( C )-( F ) Histograms of p-values from our modified version of SALT for narrow-waveform neurons recorded in one session ( C,E ) or all sessions ( D,F ) in either CFA ( C,D ) or RFA ( E,F ) while inactivating the other region. The uniformity of these distributions indicates an absence of appreciable violation of the null hypotheses that neurons are not directly activated by light. ( G )-( N ) Mean firing rate ± SEM for wide-waveform ( G–J ) or narrow-waveform ( K–N ) neurons for one animal ( G,I,K,M ) or three animals ( H,J,L,N ) recorded in CFA ( G,H,K,L ) or RFA ( I,J,M,N ) while inactivating the other region. Averages combining cells from multiple animals used the same number of cells from each animal. The cyan rectangle indicates when the light was applied. ( O )-( R ) Mean absolute firing rate change ± SEM between control and inactivation trials ( O,Q ) and mean absolute firing rate difference between control and inactivation trials averaged from 10ms after light/trial onset to 25, 50, or 100ms afterwards ( P,R ) for wide- and narrow-waveform neurons recorded in CFA ( O,P ) or RFA ( Q,R ) during inactivation of the other region. Black bars show mean across animals. ( T )-(AA) Mean firing rate ± SEM for all three animals recorded in CFA ( T,U,X,Y ) or RFA ( V,W,Z,AA ) while inactivating the other region, either for two separate sessions ( T–W ) or the first and second half of trials from all sessions ( X–AA ). The cyan rectangle indicates when the light was applied. Average inactivation effects show remarkable consistency, both within and across sessions.

    Journal: eLife

    Article Title: Hierarchy between forelimb premotor and primary motor cortices and its manifestation in their firing patterns

    doi: 10.7554/eLife.103069

    Figure Lengend Snippet: ( A ), ( B ) Histograms of waveform widths for recorded neurons in CFA ( A ) and RFA ( B ), showing the bimodal distribution of narrow and wide waveforms. Dotted line shows the threshold above which neurons were considered wide waveform. ( C )-( F ) Histograms of p-values from our modified version of SALT for narrow-waveform neurons recorded in one session ( C,E ) or all sessions ( D,F ) in either CFA ( C,D ) or RFA ( E,F ) while inactivating the other region. The uniformity of these distributions indicates an absence of appreciable violation of the null hypotheses that neurons are not directly activated by light. ( G )-( N ) Mean firing rate ± SEM for wide-waveform ( G–J ) or narrow-waveform ( K–N ) neurons for one animal ( G,I,K,M ) or three animals ( H,J,L,N ) recorded in CFA ( G,H,K,L ) or RFA ( I,J,M,N ) while inactivating the other region. Averages combining cells from multiple animals used the same number of cells from each animal. The cyan rectangle indicates when the light was applied. ( O )-( R ) Mean absolute firing rate change ± SEM between control and inactivation trials ( O,Q ) and mean absolute firing rate difference between control and inactivation trials averaged from 10ms after light/trial onset to 25, 50, or 100ms afterwards ( P,R ) for wide- and narrow-waveform neurons recorded in CFA ( O,P ) or RFA ( Q,R ) during inactivation of the other region. Black bars show mean across animals. ( T )-(AA) Mean firing rate ± SEM for all three animals recorded in CFA ( T,U,X,Y ) or RFA ( V,W,Z,AA ) while inactivating the other region, either for two separate sessions ( T–W ) or the first and second half of trials from all sessions ( X–AA ). The cyan rectangle indicates when the light was applied. Average inactivation effects show remarkable consistency, both within and across sessions.

    Article Snippet: From distributions of p-values calculated as described below for each metric, we estimated the fraction of false null hypotheses as one minus an estimate of the a prior i fraction of true null hypotheses ( ) (MATLAB function ‘mafdr’).

    Techniques: Modification, Control