Review



customized open-source software baphy  (MathWorks Inc)


Bioz Verified Symbol MathWorks Inc is a verified supplier  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 90

    Structured Review

    MathWorks Inc customized open-source software baphy
    a Experimental setup for wide-field calcium imaging showing a typical field of view in mice. Superior colliculi (SC), inferior colliculi (IC), and part of the cerebellum (Cb) are delineated in dashed orange, magenta, yellow lines, respectively. All movies are acquired at 10 Hz. b Example Δ F / F 0 images showing spontaneous events at different postnatal ages. Superior colliculi (SC), inferior colliculi (IC) are delineated in dashed orange and magenta lines, respectively. White arrowheads: spontaneous bands in the IC. White arrows: spontaneous (retinal) waves in the SC. Colormap: parula <t>(MATLAB).</t> c Example montages (Δ F / F 0 ) of spontaneous activity bands in the IC. Two magenta arrows represent major axes of the intensity profile in the left and right hemispheres. d Average peak amplitude of spontaneous activity bands across age groups. Defined as the mean Δ F / F 0 amplitude at peak. e Event frequency across age groups. Quantified as the number of individual peaks (bands) per minute as identified in the line-scan analysis. f Average normalized bandwidth across age groups. Defined as the mean spatial half-width of the fluorescence peaks normalized by the width of the IC. g Schematics for analysis of global bilateral correlations. The left hemisphere and its corresponding mean fluorescent trace are colored in blue. The right hemisphere and its mean fluorescent trace are colored in orange. A partial correlation between the two traces was computed while regressing out the effect of the mean activity overall pixels outside the IC ( r = 0.52139). h Example seed-based correlation maps at P6. Dashed magenta lines delineate symmetrical regions of interest (ROIs) in the contralateral hemisphere with respect to the reference seeds. Magenta dots denote maximum correlation in the ROIs (max r ). White dots in the left hemisphere indicates seed locations. i Example seed-based correlation maps at P12. j Average global bilateral correlation across age groups (P0–P12). k Summary quantification of seed-based bilateral correlation grouped by future frequency regions. “Low”, “mid”, and “high” corresponds to maps where reference seeds located in the putative low-, mid-, and high-frequency regions. “Averaged” correlation is defined as the mean correlation averaged over the three regions. Postnatal ages are shown on the x- axis. Box plots in Fig. 1: hinges: 25 percentile (top), 75 percentile (bottom). Box whiskers (bars): Max value (top), Min value (bottom). The line in the middle of the box is plotted at the median. Significance marks: n.s. p > 0.05, ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, **** p < 0.0001, two-tailed unpaired t test with Welch’s correction. A number of animals: P0–P1 ( N = 8); P3–P4 ( N = 11); P6–P7 ( N = 10); P9–P10 ( N = 9); P11–P12 ( N = 11); P13 ( N = 9). Scale bar indicates 1 mm. Source data and exact p values are provided as a Source Data file.
    Customized Open Source Software Baphy, 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/customized open-source software baphy/product/MathWorks Inc
    Average 90 stars, based on 1 article reviews
    customized open-source software baphy - by Bioz Stars, 2026-05
    90/100 stars

    Images

    1) Product Images from "Efferent feedback controls bilateral auditory spontaneous activity"

    Article Title: Efferent feedback controls bilateral auditory spontaneous activity

    Journal: Nature Communications

    doi: 10.1038/s41467-021-22796-8

    a Experimental setup for wide-field calcium imaging showing a typical field of view in mice. Superior colliculi (SC), inferior colliculi (IC), and part of the cerebellum (Cb) are delineated in dashed orange, magenta, yellow lines, respectively. All movies are acquired at 10 Hz. b Example Δ F / F 0 images showing spontaneous events at different postnatal ages. Superior colliculi (SC), inferior colliculi (IC) are delineated in dashed orange and magenta lines, respectively. White arrowheads: spontaneous bands in the IC. White arrows: spontaneous (retinal) waves in the SC. Colormap: parula (MATLAB). c Example montages (Δ F / F 0 ) of spontaneous activity bands in the IC. Two magenta arrows represent major axes of the intensity profile in the left and right hemispheres. d Average peak amplitude of spontaneous activity bands across age groups. Defined as the mean Δ F / F 0 amplitude at peak. e Event frequency across age groups. Quantified as the number of individual peaks (bands) per minute as identified in the line-scan analysis. f Average normalized bandwidth across age groups. Defined as the mean spatial half-width of the fluorescence peaks normalized by the width of the IC. g Schematics for analysis of global bilateral correlations. The left hemisphere and its corresponding mean fluorescent trace are colored in blue. The right hemisphere and its mean fluorescent trace are colored in orange. A partial correlation between the two traces was computed while regressing out the effect of the mean activity overall pixels outside the IC ( r = 0.52139). h Example seed-based correlation maps at P6. Dashed magenta lines delineate symmetrical regions of interest (ROIs) in the contralateral hemisphere with respect to the reference seeds. Magenta dots denote maximum correlation in the ROIs (max r ). White dots in the left hemisphere indicates seed locations. i Example seed-based correlation maps at P12. j Average global bilateral correlation across age groups (P0–P12). k Summary quantification of seed-based bilateral correlation grouped by future frequency regions. “Low”, “mid”, and “high” corresponds to maps where reference seeds located in the putative low-, mid-, and high-frequency regions. “Averaged” correlation is defined as the mean correlation averaged over the three regions. Postnatal ages are shown on the x- axis. Box plots in Fig. 1: hinges: 25 percentile (top), 75 percentile (bottom). Box whiskers (bars): Max value (top), Min value (bottom). The line in the middle of the box is plotted at the median. Significance marks: n.s. p > 0.05, ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, **** p < 0.0001, two-tailed unpaired t test with Welch’s correction. A number of animals: P0–P1 ( N = 8); P3–P4 ( N = 11); P6–P7 ( N = 10); P9–P10 ( N = 9); P11–P12 ( N = 11); P13 ( N = 9). Scale bar indicates 1 mm. Source data and exact p values are provided as a Source Data file.
    Figure Legend Snippet: a Experimental setup for wide-field calcium imaging showing a typical field of view in mice. Superior colliculi (SC), inferior colliculi (IC), and part of the cerebellum (Cb) are delineated in dashed orange, magenta, yellow lines, respectively. All movies are acquired at 10 Hz. b Example Δ F / F 0 images showing spontaneous events at different postnatal ages. Superior colliculi (SC), inferior colliculi (IC) are delineated in dashed orange and magenta lines, respectively. White arrowheads: spontaneous bands in the IC. White arrows: spontaneous (retinal) waves in the SC. Colormap: parula (MATLAB). c Example montages (Δ F / F 0 ) of spontaneous activity bands in the IC. Two magenta arrows represent major axes of the intensity profile in the left and right hemispheres. d Average peak amplitude of spontaneous activity bands across age groups. Defined as the mean Δ F / F 0 amplitude at peak. e Event frequency across age groups. Quantified as the number of individual peaks (bands) per minute as identified in the line-scan analysis. f Average normalized bandwidth across age groups. Defined as the mean spatial half-width of the fluorescence peaks normalized by the width of the IC. g Schematics for analysis of global bilateral correlations. The left hemisphere and its corresponding mean fluorescent trace are colored in blue. The right hemisphere and its mean fluorescent trace are colored in orange. A partial correlation between the two traces was computed while regressing out the effect of the mean activity overall pixels outside the IC ( r = 0.52139). h Example seed-based correlation maps at P6. Dashed magenta lines delineate symmetrical regions of interest (ROIs) in the contralateral hemisphere with respect to the reference seeds. Magenta dots denote maximum correlation in the ROIs (max r ). White dots in the left hemisphere indicates seed locations. i Example seed-based correlation maps at P12. j Average global bilateral correlation across age groups (P0–P12). k Summary quantification of seed-based bilateral correlation grouped by future frequency regions. “Low”, “mid”, and “high” corresponds to maps where reference seeds located in the putative low-, mid-, and high-frequency regions. “Averaged” correlation is defined as the mean correlation averaged over the three regions. Postnatal ages are shown on the x- axis. Box plots in Fig. 1: hinges: 25 percentile (top), 75 percentile (bottom). Box whiskers (bars): Max value (top), Min value (bottom). The line in the middle of the box is plotted at the median. Significance marks: n.s. p > 0.05, ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, **** p < 0.0001, two-tailed unpaired t test with Welch’s correction. A number of animals: P0–P1 ( N = 8); P3–P4 ( N = 11); P6–P7 ( N = 10); P9–P10 ( N = 9); P11–P12 ( N = 11); P13 ( N = 9). Scale bar indicates 1 mm. Source data and exact p values are provided as a Source Data file.

    Techniques Used: Imaging, Activity Assay, Fluorescence, Two Tailed Test

    a Snapshots of example auditory brainstem response (ABR) curves. White arrowheads indicate ABR waves. Scale bar indicates 2 µV. The White dashed line represents the detection threshold. b Auditory thresholds measured by auditory brainstem response (ABR) in control and α9/α10 nAChR knockout animals at P14.0. A number of animals: Control P14.0 = 9 (GCaMP6s negative littermates of animals used in ( e )). α9/α10 knockout P14.0 = 6. Magenta arrowheads indicate that part of the data is not available in the knockout group (two animals did not respond to 4 kHz tones.). n.s., two-way ANOVA, F = 1.409, p = 0.0604 on the column (genotype) factor. c Auditory thresholds measured by wide-field imaging. A number of animals: Control = 8 (wide-type SNAP25-G6s = 6; α9/α10 double heterozygous SNAP25-G6s = 2). Knockout = 8 (mix of single knockout of either α9 or α10 subunit and double knockout). Two-way ANOVA, F = 31.98, **** p < 0.0001 on the column (genotype) factor. d Example Δ F / F 0 response images to different acoustic stimuli. Row direction: Sound level. Column direction: frequency. Solid magenta lines denote the auditory thresholds at different frequencies. Dashed red rectangles highlight columns of responses to different frequencies at the same SPL level (tonotopy). Het heterozygous, KO knockout. Colormap: parula (MATLAB). Top image array: an example from a P14.0 α9/α10 double heterozygous control. Bottom image array: an example from its P14.0 α9 knockout α10 heterozygous littermate. Schematics in the middle: major axes and tonotopic reversals in the two hemispheres of the IC. Box plots in Fig. 5: hinges: 25 percentile (top), 75 percentile (bottom). Box whiskers (bars): Max value (top), Min value (bottom). Source data and exact p values are provided as a Source Data file.
    Figure Legend Snippet: a Snapshots of example auditory brainstem response (ABR) curves. White arrowheads indicate ABR waves. Scale bar indicates 2 µV. The White dashed line represents the detection threshold. b Auditory thresholds measured by auditory brainstem response (ABR) in control and α9/α10 nAChR knockout animals at P14.0. A number of animals: Control P14.0 = 9 (GCaMP6s negative littermates of animals used in ( e )). α9/α10 knockout P14.0 = 6. Magenta arrowheads indicate that part of the data is not available in the knockout group (two animals did not respond to 4 kHz tones.). n.s., two-way ANOVA, F = 1.409, p = 0.0604 on the column (genotype) factor. c Auditory thresholds measured by wide-field imaging. A number of animals: Control = 8 (wide-type SNAP25-G6s = 6; α9/α10 double heterozygous SNAP25-G6s = 2). Knockout = 8 (mix of single knockout of either α9 or α10 subunit and double knockout). Two-way ANOVA, F = 31.98, **** p < 0.0001 on the column (genotype) factor. d Example Δ F / F 0 response images to different acoustic stimuli. Row direction: Sound level. Column direction: frequency. Solid magenta lines denote the auditory thresholds at different frequencies. Dashed red rectangles highlight columns of responses to different frequencies at the same SPL level (tonotopy). Het heterozygous, KO knockout. Colormap: parula (MATLAB). Top image array: an example from a P14.0 α9/α10 double heterozygous control. Bottom image array: an example from its P14.0 α9 knockout α10 heterozygous littermate. Schematics in the middle: major axes and tonotopic reversals in the two hemispheres of the IC. Box plots in Fig. 5: hinges: 25 percentile (top), 75 percentile (bottom). Box whiskers (bars): Max value (top), Min value (bottom). Source data and exact p values are provided as a Source Data file.

    Techniques Used: Control, Knock-Out, Imaging, Double Knockout



    Similar Products

    90
    MathWorks Inc customized open-source software baphy
    a Experimental setup for wide-field calcium imaging showing a typical field of view in mice. Superior colliculi (SC), inferior colliculi (IC), and part of the cerebellum (Cb) are delineated in dashed orange, magenta, yellow lines, respectively. All movies are acquired at 10 Hz. b Example Δ F / F 0 images showing spontaneous events at different postnatal ages. Superior colliculi (SC), inferior colliculi (IC) are delineated in dashed orange and magenta lines, respectively. White arrowheads: spontaneous bands in the IC. White arrows: spontaneous (retinal) waves in the SC. Colormap: parula <t>(MATLAB).</t> c Example montages (Δ F / F 0 ) of spontaneous activity bands in the IC. Two magenta arrows represent major axes of the intensity profile in the left and right hemispheres. d Average peak amplitude of spontaneous activity bands across age groups. Defined as the mean Δ F / F 0 amplitude at peak. e Event frequency across age groups. Quantified as the number of individual peaks (bands) per minute as identified in the line-scan analysis. f Average normalized bandwidth across age groups. Defined as the mean spatial half-width of the fluorescence peaks normalized by the width of the IC. g Schematics for analysis of global bilateral correlations. The left hemisphere and its corresponding mean fluorescent trace are colored in blue. The right hemisphere and its mean fluorescent trace are colored in orange. A partial correlation between the two traces was computed while regressing out the effect of the mean activity overall pixels outside the IC ( r = 0.52139). h Example seed-based correlation maps at P6. Dashed magenta lines delineate symmetrical regions of interest (ROIs) in the contralateral hemisphere with respect to the reference seeds. Magenta dots denote maximum correlation in the ROIs (max r ). White dots in the left hemisphere indicates seed locations. i Example seed-based correlation maps at P12. j Average global bilateral correlation across age groups (P0–P12). k Summary quantification of seed-based bilateral correlation grouped by future frequency regions. “Low”, “mid”, and “high” corresponds to maps where reference seeds located in the putative low-, mid-, and high-frequency regions. “Averaged” correlation is defined as the mean correlation averaged over the three regions. Postnatal ages are shown on the x- axis. Box plots in Fig. 1: hinges: 25 percentile (top), 75 percentile (bottom). Box whiskers (bars): Max value (top), Min value (bottom). The line in the middle of the box is plotted at the median. Significance marks: n.s. p > 0.05, ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, **** p < 0.0001, two-tailed unpaired t test with Welch’s correction. A number of animals: P0–P1 ( N = 8); P3–P4 ( N = 11); P6–P7 ( N = 10); P9–P10 ( N = 9); P11–P12 ( N = 11); P13 ( N = 9). Scale bar indicates 1 mm. Source data and exact p values are provided as a Source Data file.
    Customized Open Source Software Baphy, 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/customized open-source software baphy/product/MathWorks Inc
    Average 90 stars, based on 1 article reviews
    customized open-source software baphy - by Bioz Stars, 2026-05
    90/100 stars
      Buy from Supplier

    Image Search Results


    a Experimental setup for wide-field calcium imaging showing a typical field of view in mice. Superior colliculi (SC), inferior colliculi (IC), and part of the cerebellum (Cb) are delineated in dashed orange, magenta, yellow lines, respectively. All movies are acquired at 10 Hz. b Example Δ F / F 0 images showing spontaneous events at different postnatal ages. Superior colliculi (SC), inferior colliculi (IC) are delineated in dashed orange and magenta lines, respectively. White arrowheads: spontaneous bands in the IC. White arrows: spontaneous (retinal) waves in the SC. Colormap: parula (MATLAB). c Example montages (Δ F / F 0 ) of spontaneous activity bands in the IC. Two magenta arrows represent major axes of the intensity profile in the left and right hemispheres. d Average peak amplitude of spontaneous activity bands across age groups. Defined as the mean Δ F / F 0 amplitude at peak. e Event frequency across age groups. Quantified as the number of individual peaks (bands) per minute as identified in the line-scan analysis. f Average normalized bandwidth across age groups. Defined as the mean spatial half-width of the fluorescence peaks normalized by the width of the IC. g Schematics for analysis of global bilateral correlations. The left hemisphere and its corresponding mean fluorescent trace are colored in blue. The right hemisphere and its mean fluorescent trace are colored in orange. A partial correlation between the two traces was computed while regressing out the effect of the mean activity overall pixels outside the IC ( r = 0.52139). h Example seed-based correlation maps at P6. Dashed magenta lines delineate symmetrical regions of interest (ROIs) in the contralateral hemisphere with respect to the reference seeds. Magenta dots denote maximum correlation in the ROIs (max r ). White dots in the left hemisphere indicates seed locations. i Example seed-based correlation maps at P12. j Average global bilateral correlation across age groups (P0–P12). k Summary quantification of seed-based bilateral correlation grouped by future frequency regions. “Low”, “mid”, and “high” corresponds to maps where reference seeds located in the putative low-, mid-, and high-frequency regions. “Averaged” correlation is defined as the mean correlation averaged over the three regions. Postnatal ages are shown on the x- axis. Box plots in Fig. 1: hinges: 25 percentile (top), 75 percentile (bottom). Box whiskers (bars): Max value (top), Min value (bottom). The line in the middle of the box is plotted at the median. Significance marks: n.s. p > 0.05, ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, **** p < 0.0001, two-tailed unpaired t test with Welch’s correction. A number of animals: P0–P1 ( N = 8); P3–P4 ( N = 11); P6–P7 ( N = 10); P9–P10 ( N = 9); P11–P12 ( N = 11); P13 ( N = 9). Scale bar indicates 1 mm. Source data and exact p values are provided as a Source Data file.

    Journal: Nature Communications

    Article Title: Efferent feedback controls bilateral auditory spontaneous activity

    doi: 10.1038/s41467-021-22796-8

    Figure Lengend Snippet: a Experimental setup for wide-field calcium imaging showing a typical field of view in mice. Superior colliculi (SC), inferior colliculi (IC), and part of the cerebellum (Cb) are delineated in dashed orange, magenta, yellow lines, respectively. All movies are acquired at 10 Hz. b Example Δ F / F 0 images showing spontaneous events at different postnatal ages. Superior colliculi (SC), inferior colliculi (IC) are delineated in dashed orange and magenta lines, respectively. White arrowheads: spontaneous bands in the IC. White arrows: spontaneous (retinal) waves in the SC. Colormap: parula (MATLAB). c Example montages (Δ F / F 0 ) of spontaneous activity bands in the IC. Two magenta arrows represent major axes of the intensity profile in the left and right hemispheres. d Average peak amplitude of spontaneous activity bands across age groups. Defined as the mean Δ F / F 0 amplitude at peak. e Event frequency across age groups. Quantified as the number of individual peaks (bands) per minute as identified in the line-scan analysis. f Average normalized bandwidth across age groups. Defined as the mean spatial half-width of the fluorescence peaks normalized by the width of the IC. g Schematics for analysis of global bilateral correlations. The left hemisphere and its corresponding mean fluorescent trace are colored in blue. The right hemisphere and its mean fluorescent trace are colored in orange. A partial correlation between the two traces was computed while regressing out the effect of the mean activity overall pixels outside the IC ( r = 0.52139). h Example seed-based correlation maps at P6. Dashed magenta lines delineate symmetrical regions of interest (ROIs) in the contralateral hemisphere with respect to the reference seeds. Magenta dots denote maximum correlation in the ROIs (max r ). White dots in the left hemisphere indicates seed locations. i Example seed-based correlation maps at P12. j Average global bilateral correlation across age groups (P0–P12). k Summary quantification of seed-based bilateral correlation grouped by future frequency regions. “Low”, “mid”, and “high” corresponds to maps where reference seeds located in the putative low-, mid-, and high-frequency regions. “Averaged” correlation is defined as the mean correlation averaged over the three regions. Postnatal ages are shown on the x- axis. Box plots in Fig. 1: hinges: 25 percentile (top), 75 percentile (bottom). Box whiskers (bars): Max value (top), Min value (bottom). The line in the middle of the box is plotted at the median. Significance marks: n.s. p > 0.05, ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, **** p < 0.0001, two-tailed unpaired t test with Welch’s correction. A number of animals: P0–P1 ( N = 8); P3–P4 ( N = 11); P6–P7 ( N = 10); P9–P10 ( N = 9); P11–P12 ( N = 11); P13 ( N = 9). Scale bar indicates 1 mm. Source data and exact p values are provided as a Source Data file.

    Article Snippet: Acoustic stimuli were generated with customized open-source software in MATLAB (“Baphy”, Neural Systems Laboratory, University of Maryland College Park).

    Techniques: Imaging, Activity Assay, Fluorescence, Two Tailed Test

    a Snapshots of example auditory brainstem response (ABR) curves. White arrowheads indicate ABR waves. Scale bar indicates 2 µV. The White dashed line represents the detection threshold. b Auditory thresholds measured by auditory brainstem response (ABR) in control and α9/α10 nAChR knockout animals at P14.0. A number of animals: Control P14.0 = 9 (GCaMP6s negative littermates of animals used in ( e )). α9/α10 knockout P14.0 = 6. Magenta arrowheads indicate that part of the data is not available in the knockout group (two animals did not respond to 4 kHz tones.). n.s., two-way ANOVA, F = 1.409, p = 0.0604 on the column (genotype) factor. c Auditory thresholds measured by wide-field imaging. A number of animals: Control = 8 (wide-type SNAP25-G6s = 6; α9/α10 double heterozygous SNAP25-G6s = 2). Knockout = 8 (mix of single knockout of either α9 or α10 subunit and double knockout). Two-way ANOVA, F = 31.98, **** p < 0.0001 on the column (genotype) factor. d Example Δ F / F 0 response images to different acoustic stimuli. Row direction: Sound level. Column direction: frequency. Solid magenta lines denote the auditory thresholds at different frequencies. Dashed red rectangles highlight columns of responses to different frequencies at the same SPL level (tonotopy). Het heterozygous, KO knockout. Colormap: parula (MATLAB). Top image array: an example from a P14.0 α9/α10 double heterozygous control. Bottom image array: an example from its P14.0 α9 knockout α10 heterozygous littermate. Schematics in the middle: major axes and tonotopic reversals in the two hemispheres of the IC. Box plots in Fig. 5: hinges: 25 percentile (top), 75 percentile (bottom). Box whiskers (bars): Max value (top), Min value (bottom). Source data and exact p values are provided as a Source Data file.

    Journal: Nature Communications

    Article Title: Efferent feedback controls bilateral auditory spontaneous activity

    doi: 10.1038/s41467-021-22796-8

    Figure Lengend Snippet: a Snapshots of example auditory brainstem response (ABR) curves. White arrowheads indicate ABR waves. Scale bar indicates 2 µV. The White dashed line represents the detection threshold. b Auditory thresholds measured by auditory brainstem response (ABR) in control and α9/α10 nAChR knockout animals at P14.0. A number of animals: Control P14.0 = 9 (GCaMP6s negative littermates of animals used in ( e )). α9/α10 knockout P14.0 = 6. Magenta arrowheads indicate that part of the data is not available in the knockout group (two animals did not respond to 4 kHz tones.). n.s., two-way ANOVA, F = 1.409, p = 0.0604 on the column (genotype) factor. c Auditory thresholds measured by wide-field imaging. A number of animals: Control = 8 (wide-type SNAP25-G6s = 6; α9/α10 double heterozygous SNAP25-G6s = 2). Knockout = 8 (mix of single knockout of either α9 or α10 subunit and double knockout). Two-way ANOVA, F = 31.98, **** p < 0.0001 on the column (genotype) factor. d Example Δ F / F 0 response images to different acoustic stimuli. Row direction: Sound level. Column direction: frequency. Solid magenta lines denote the auditory thresholds at different frequencies. Dashed red rectangles highlight columns of responses to different frequencies at the same SPL level (tonotopy). Het heterozygous, KO knockout. Colormap: parula (MATLAB). Top image array: an example from a P14.0 α9/α10 double heterozygous control. Bottom image array: an example from its P14.0 α9 knockout α10 heterozygous littermate. Schematics in the middle: major axes and tonotopic reversals in the two hemispheres of the IC. Box plots in Fig. 5: hinges: 25 percentile (top), 75 percentile (bottom). Box whiskers (bars): Max value (top), Min value (bottom). Source data and exact p values are provided as a Source Data file.

    Article Snippet: Acoustic stimuli were generated with customized open-source software in MATLAB (“Baphy”, Neural Systems Laboratory, University of Maryland College Park).

    Techniques: Control, Knock-Out, Imaging, Double Knockout