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mafdr function  (MathWorks Inc)


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    MathWorks Inc mafdr function
    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/result/mafdr function/product/MathWorks Inc
    Average 90 stars, based on 1 article reviews
    mafdr function - by Bioz Stars, 2026-03
    90/100 stars

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    MathWorks Inc mafdr function
    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/result/mafdr function/product/MathWorks Inc
    Average 90 stars, based on 1 article reviews
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    MathWorks Inc matlab function 'mafdr
    ( 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
    https://www.bioz.com/result/matlab function 'mafdr/product/MathWorks Inc
    Average 90 stars, based on 1 article reviews
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    MathWorks Inc matlab function mafdr
    ( 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
    https://www.bioz.com/result/matlab function mafdr/product/MathWorks Inc
    Average 90 stars, based on 1 article reviews
    matlab function mafdr - by Bioz Stars, 2026-03
    90/100 stars
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    90
    MathWorks Inc matlab mafdr-function
    ( 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/result/matlab mafdr-function/product/MathWorks Inc
    Average 90 stars, based on 1 article reviews
    matlab mafdr-function - by Bioz Stars, 2026-03
    90/100 stars
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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 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