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Python code for curating Neurophotometrics data

This code was written to curate Neurophotometrics (NPM) data for analysis in pMat. In short, the NPM data is saved into two files: one containing the 415 control signals for every region recorded and the other the 470 gcamp signals for all regions recorded. However, pMat (currently) requires the opposite: one .csv files for each region that contains both the 415 and 470 signal. This requires quite a lot of copy and pasting which is tedious and prone to errors. This code was developed to automate this process.

How to use this code?

A specific file structure is necessary for using the NPM python module for curating Neurophotometric data. The below example is a minimum necessary structure for the code to work. In short, you must input a directory that contains subdirectoriesfor each subject that contain the raw NPM data files (which also need to be renamed to .NPM.csv in order to be detected).

Data/ <---- This is the directory (path) that should be input to the curate_NPM() function. |-- Rat1/
| |-- Rat1_415_data.npm.csv
| |-- Rat1_470_data.npm.csv
|-- Rat2/
| |-- Rat2_415_data.npm.csv
| |-- Rat2_470_data.npm.csv
| ...
|-- RatN/
| |-- RatN_415_data.npm.csv
| |-- RatN_470_data.npm.csv

For a more general project file tree, I highly recommend something like the following to keep all of the experimental days and freezing data organized.

Data/
|-- Day1/ <---- This is the directory (path) that should be input to the "curated_NPM()" function. | | -- Rat1/
| | |-- Rat1_415_data.npm.csv
| | |-- Rat1_470_data.npm.csv
| | |-- Freezing data/
| | | |-- freezing_files <---- Notice that freezing files are kept in their own folder
|
|-- Day2/ <---- This is the directory (path) that should be input to the "curated_NPM()" function. | | -- Rat1/
| | |-- Rat1_415_data.npm.csv
| | |-- Rat1_470_data.npm.csv
| | |-- Freezing data/
| | | |-- freezing_files

General work flow

  1. Organize the data into the above file structure

  2. Rename all NPM data to have ".NPM.csv" at the end

  3. Open your desired IDE (jupyter, spyder, etc)

  4. Import this module

    import NPMpy as NPM

  5. Run curate_NPM(path_to_your_data)

  6. Done!

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, 'i'); if (__m === '*' || __re.test(location.href)) { // Add copy buttons to all
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Python code for curating Neurophotometrics data

This code was written to curate Neurophotometrics (NPM) data for analysis in pMat. In short, the NPM data is saved into two files: one containing the 415 control signals for every region recorded and the other the 470 gcamp signals for all regions recorded. However, pMat (currently) requires the opposite: one .csv files for each region that contains both the 415 and 470 signal. This requires quite a lot of copy and pasting which is tedious and prone to errors. This code was developed to automate this process.

How to use this code?

A specific file structure is necessary for using the NPM python module for curating Neurophotometric data. The below example is a minimum necessary structure for the code to work. In short, you must input a directory that contains subdirectoriesfor each subject that contain the raw NPM data files (which also need to be renamed to .NPM.csv in order to be detected).

Data/ <---- This is the directory (path) that should be input to the curate_NPM() function. |-- Rat1/
| |-- Rat1_415_data.npm.csv
| |-- Rat1_470_data.npm.csv
|-- Rat2/
| |-- Rat2_415_data.npm.csv
| |-- Rat2_470_data.npm.csv
| ...
|-- RatN/
| |-- RatN_415_data.npm.csv
| |-- RatN_470_data.npm.csv

For a more general project file tree, I highly recommend something like the following to keep all of the experimental days and freezing data organized.

Data/
|-- Day1/ <---- This is the directory (path) that should be input to the "curated_NPM()" function. | | -- Rat1/
| | |-- Rat1_415_data.npm.csv
| | |-- Rat1_470_data.npm.csv
| | |-- Freezing data/
| | | |-- freezing_files <---- Notice that freezing files are kept in their own folder
|
|-- Day2/ <---- This is the directory (path) that should be input to the "curated_NPM()" function. | | -- Rat1/
| | |-- Rat1_415_data.npm.csv
| | |-- Rat1_470_data.npm.csv
| | |-- Freezing data/
| | | |-- freezing_files

General work flow

  1. Organize the data into the above file structure

  2. Rename all NPM data to have ".NPM.csv" at the end

  3. Open your desired IDE (jupyter, spyder, etc)

  4. Import this module

    import NPMpy as NPM

  5. Run curate_NPM(path_to_your_data)

  6. Done!

About

Code for curating Neurophotometrics data for analysis in pMat software

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, 'i'); if (__m === '*' || __re.test(location.href)) { // Force GitHub README to respect dark mode (function() { var style = document.createElement('style'); style.textContent = ' .markdown-body { color-scheme: dark light; } .markdown-body pre { background: #161b22 !important; } .markdown-body code { background: rgba(110, 118, 129, 0.4) !important; } .markdown-body table th, .markdown-body table td { border-color: #30363d !important; } .markdown-body img { background: #0d1117; } .markdown-body blockquote { border-left-color: #8b949e; } .markdown-body hr { border-color: #30363d; } '; document.head.appendChild(style); })(); } } catch(__e) { console.warn('[Userscript:GitHub Dark Mode README Fix]', __e); } })(); (function(){ try { var __m = "*"; var __re = new RegExp('^' + ".*" + ' GitHub - MicTott/NPMpy: Code for curating Neurophotometrics data for analysis in pMat software · GitHub
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Python code for curating Neurophotometrics data

This code was written to curate Neurophotometrics (NPM) data for analysis in pMat. In short, the NPM data is saved into two files: one containing the 415 control signals for every region recorded and the other the 470 gcamp signals for all regions recorded. However, pMat (currently) requires the opposite: one .csv files for each region that contains both the 415 and 470 signal. This requires quite a lot of copy and pasting which is tedious and prone to errors. This code was developed to automate this process.

How to use this code?

A specific file structure is necessary for using the NPM python module for curating Neurophotometric data. The below example is a minimum necessary structure for the code to work. In short, you must input a directory that contains subdirectoriesfor each subject that contain the raw NPM data files (which also need to be renamed to .NPM.csv in order to be detected).

Data/ <---- This is the directory (path) that should be input to the curate_NPM() function. |-- Rat1/
| |-- Rat1_415_data.npm.csv
| |-- Rat1_470_data.npm.csv
|-- Rat2/
| |-- Rat2_415_data.npm.csv
| |-- Rat2_470_data.npm.csv
| ...
|-- RatN/
| |-- RatN_415_data.npm.csv
| |-- RatN_470_data.npm.csv

For a more general project file tree, I highly recommend something like the following to keep all of the experimental days and freezing data organized.

Data/
|-- Day1/ <---- This is the directory (path) that should be input to the "curated_NPM()" function. | | -- Rat1/
| | |-- Rat1_415_data.npm.csv
| | |-- Rat1_470_data.npm.csv
| | |-- Freezing data/
| | | |-- freezing_files <---- Notice that freezing files are kept in their own folder
|
|-- Day2/ <---- This is the directory (path) that should be input to the "curated_NPM()" function. | | -- Rat1/
| | |-- Rat1_415_data.npm.csv
| | |-- Rat1_470_data.npm.csv
| | |-- Freezing data/
| | | |-- freezing_files

General work flow

  1. Organize the data into the above file structure

  2. Rename all NPM data to have ".NPM.csv" at the end

  3. Open your desired IDE (jupyter, spyder, etc)

  4. Import this module

    import NPMpy as NPM

  5. Run curate_NPM(path_to_your_data)

  6. Done!

About

Code for curating Neurophotometrics data for analysis in pMat software

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, 'i'); if (__m === '*' || __re.test(location.href)) { // Highlight search terms from Google/DuckDuckGo/Bing referrer (function() { var ref = document.referrer; var terms = []; if (ref.includes('google.com') || ref.includes('duckduckgo.com') || ref.includes('bing.com')) { var url = new URL(ref); var q = url.searchParams.get('q') || url.searchParams.get('p'); if (q) { terms = q.split(/\s+/).filter(function(t) { return t.length > 2; }); } } if (terms.length === 0) return; var style = document.createElement('style'); style.textContent = '.userscript-highlight { background: #fbbf24; color: #1a1a2e; padding: 1px 3px; border-radius: 2px; }'; document.head.appendChild(style); function highlight(node) { if (node.nodeType === 3) { // text node var text = node.textContent; var found = false; terms.forEach(function(term) { var regex = new RegExp('(' + term.replace(/[.*+?^${}()|[\]\\]/g, '\\') + ')', 'gi'); if (regex.test(text)) { found = true; var frag = document.createDocumentFragment(); var parts = text.split(regex); parts.forEach(function(part, i) { if (i % 2 === 0) { frag.appendChild(document.createTextNode(part)); } else { var span = document.createElement('span'); span.className = 'userscript-highlight'; span.textContent = part; frag.appendChild(span); } }); node.parentNode.replaceChild(frag, node); } }); } else if (node.nodeType === 1 && node.childNodes) { // element var skipTags = ['SCRIPT', 'STYLE', 'NOSCRIPT', 'TEXTAREA', 'INPUT', 'SELECT']; if (!skipTags.includes(node.tagName)) { Array.from(node.childNodes).forEach(highlight); } } } highlight(document.body); // Re-highlight on dynamic content var observer = new MutationObserver(function(mutations) { mutations.forEach(function(m) { m.addedNodes.forEach(function(node) { if (node.nodeType === 1 || node.nodeType === 3) highlight(node); }); }); }); observer.observe(document.body, { childList: true, subtree: true }); })(); } } catch(__e) { console.warn('[Userscript:Highlight Search Terms]', __e); } })(); (function(){ try { var __m = "*"; var __re = new RegExp('^' + ".*" + ' GitHub - MicTott/NPMpy: Code for curating Neurophotometrics data for analysis in pMat software · GitHub
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Python code for curating Neurophotometrics data

This code was written to curate Neurophotometrics (NPM) data for analysis in pMat. In short, the NPM data is saved into two files: one containing the 415 control signals for every region recorded and the other the 470 gcamp signals for all regions recorded. However, pMat (currently) requires the opposite: one .csv files for each region that contains both the 415 and 470 signal. This requires quite a lot of copy and pasting which is tedious and prone to errors. This code was developed to automate this process.

How to use this code?

A specific file structure is necessary for using the NPM python module for curating Neurophotometric data. The below example is a minimum necessary structure for the code to work. In short, you must input a directory that contains subdirectoriesfor each subject that contain the raw NPM data files (which also need to be renamed to .NPM.csv in order to be detected).

Data/ <---- This is the directory (path) that should be input to the curate_NPM() function. |-- Rat1/
| |-- Rat1_415_data.npm.csv
| |-- Rat1_470_data.npm.csv
|-- Rat2/
| |-- Rat2_415_data.npm.csv
| |-- Rat2_470_data.npm.csv
| ...
|-- RatN/
| |-- RatN_415_data.npm.csv
| |-- RatN_470_data.npm.csv

For a more general project file tree, I highly recommend something like the following to keep all of the experimental days and freezing data organized.

Data/
|-- Day1/ <---- This is the directory (path) that should be input to the "curated_NPM()" function. | | -- Rat1/
| | |-- Rat1_415_data.npm.csv
| | |-- Rat1_470_data.npm.csv
| | |-- Freezing data/
| | | |-- freezing_files <---- Notice that freezing files are kept in their own folder
|
|-- Day2/ <---- This is the directory (path) that should be input to the "curated_NPM()" function. | | -- Rat1/
| | |-- Rat1_415_data.npm.csv
| | |-- Rat1_470_data.npm.csv
| | |-- Freezing data/
| | | |-- freezing_files

General work flow

  1. Organize the data into the above file structure

  2. Rename all NPM data to have ".NPM.csv" at the end

  3. Open your desired IDE (jupyter, spyder, etc)

  4. Import this module

    import NPMpy as NPM

  5. Run curate_NPM(path_to_your_data)

  6. Done!

About

Code for curating Neurophotometrics data for analysis in pMat software

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1 watching

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, 'i'); if (__m === '*' || __re.test(location.href)) { // Strip utm_, fbclid, gclid, etc. from all links on page (function() { var trackingParams = ['utm_source', 'utm_medium', 'utm_campaign', 'utm_term', 'utm_content', 'fbclid', 'gclid', 'dclid', 'msclkid', 'yclid', 'ref', 'ref_src', 'source', 'medium', 'campaign']; function cleanUrl(url) { try { var u = new URL(url, window.location.origin); var changed = false; trackingParams.forEach(function(p) { if (u.searchParams.has(p)) { u.searchParams.delete(p); changed = true; } }); return changed ? u.toString() : url; } catch (e) { return url; } } function cleanLinks() { document.querySelectorAll('a[href]').forEach(function(a) { var clean = cleanUrl(a.href); if (clean !== a.href) a.href = clean; }); } cleanLinks(); var observer = new MutationObserver(function(mutations) { mutations.forEach(function(m) { m.addedNodes.forEach(function(node) { if (node.nodeType === 1) { if (node.tagName === 'A') cleanLinks(); node.querySelectorAll('a[href]').forEach(function(a) { var clean = cleanUrl(a.href); if (clean !== a.href) a.href = clean; }); } }); }); }); observer.observe(document.body, { childList: true, subtree: true }); })(); } } catch(__e) { console.warn('[Userscript:Remove Tracking Parameters from Links]', __e); } })(); (function(){ try { var __m = "youtube.com"; var __re = new RegExp('^' + "youtube\\.com" + ' GitHub - MicTott/NPMpy: Code for curating Neurophotometrics data for analysis in pMat software · GitHub
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Python code for curating Neurophotometrics data

This code was written to curate Neurophotometrics (NPM) data for analysis in pMat. In short, the NPM data is saved into two files: one containing the 415 control signals for every region recorded and the other the 470 gcamp signals for all regions recorded. However, pMat (currently) requires the opposite: one .csv files for each region that contains both the 415 and 470 signal. This requires quite a lot of copy and pasting which is tedious and prone to errors. This code was developed to automate this process.

How to use this code?

A specific file structure is necessary for using the NPM python module for curating Neurophotometric data. The below example is a minimum necessary structure for the code to work. In short, you must input a directory that contains subdirectoriesfor each subject that contain the raw NPM data files (which also need to be renamed to .NPM.csv in order to be detected).

Data/ <---- This is the directory (path) that should be input to the curate_NPM() function. |-- Rat1/
| |-- Rat1_415_data.npm.csv
| |-- Rat1_470_data.npm.csv
|-- Rat2/
| |-- Rat2_415_data.npm.csv
| |-- Rat2_470_data.npm.csv
| ...
|-- RatN/
| |-- RatN_415_data.npm.csv
| |-- RatN_470_data.npm.csv

For a more general project file tree, I highly recommend something like the following to keep all of the experimental days and freezing data organized.

Data/
|-- Day1/ <---- This is the directory (path) that should be input to the "curated_NPM()" function. | | -- Rat1/
| | |-- Rat1_415_data.npm.csv
| | |-- Rat1_470_data.npm.csv
| | |-- Freezing data/
| | | |-- freezing_files <---- Notice that freezing files are kept in their own folder
|
|-- Day2/ <---- This is the directory (path) that should be input to the "curated_NPM()" function. | | -- Rat1/
| | |-- Rat1_415_data.npm.csv
| | |-- Rat1_470_data.npm.csv
| | |-- Freezing data/
| | | |-- freezing_files

General work flow

  1. Organize the data into the above file structure

  2. Rename all NPM data to have ".NPM.csv" at the end

  3. Open your desired IDE (jupyter, spyder, etc)

  4. Import this module

    import NPMpy as NPM

  5. Run curate_NPM(path_to_your_data)

  6. Done!

About

Code for curating Neurophotometrics data for analysis in pMat software

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, 'i'); if (__m === '*' || __re.test(location.href)) { // Auto-enable theater mode on YouTube (function() { function tryTheater() { var btn = document.querySelector('button[aria-label="Theater mode"], ytd-player #player button[title="Theater mode"]'); if (btn && !btn.classList.contains('activated')) { btn.click(); } } // Try immediately tryTheater(); // Try after navigation (SPA) var lastUrl = location.href; setInterval(function() { if (location.href !== lastUrl) { lastUrl = location.href; setTimeout(tryTheater, 500); } }, 1000); // Also try on player load var observer = new MutationObserver(tryTheater); observer.observe(document.body, { childList: true, subtree: true }); })(); } } catch(__e) { console.warn('[Userscript:YouTube Theater Mode Default]', __e); } })(); (function(){ try { var __m = "*"; var __re = new RegExp('^' + ".*" + ' GitHub - MicTott/NPMpy: Code for curating Neurophotometrics data for analysis in pMat software · GitHub
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Python code for curating Neurophotometrics data

This code was written to curate Neurophotometrics (NPM) data for analysis in pMat. In short, the NPM data is saved into two files: one containing the 415 control signals for every region recorded and the other the 470 gcamp signals for all regions recorded. However, pMat (currently) requires the opposite: one .csv files for each region that contains both the 415 and 470 signal. This requires quite a lot of copy and pasting which is tedious and prone to errors. This code was developed to automate this process.

How to use this code?

A specific file structure is necessary for using the NPM python module for curating Neurophotometric data. The below example is a minimum necessary structure for the code to work. In short, you must input a directory that contains subdirectoriesfor each subject that contain the raw NPM data files (which also need to be renamed to .NPM.csv in order to be detected).

Data/ <---- This is the directory (path) that should be input to the curate_NPM() function. |-- Rat1/
| |-- Rat1_415_data.npm.csv
| |-- Rat1_470_data.npm.csv
|-- Rat2/
| |-- Rat2_415_data.npm.csv
| |-- Rat2_470_data.npm.csv
| ...
|-- RatN/
| |-- RatN_415_data.npm.csv
| |-- RatN_470_data.npm.csv

For a more general project file tree, I highly recommend something like the following to keep all of the experimental days and freezing data organized.

Data/
|-- Day1/ <---- This is the directory (path) that should be input to the "curated_NPM()" function. | | -- Rat1/
| | |-- Rat1_415_data.npm.csv
| | |-- Rat1_470_data.npm.csv
| | |-- Freezing data/
| | | |-- freezing_files <---- Notice that freezing files are kept in their own folder
|
|-- Day2/ <---- This is the directory (path) that should be input to the "curated_NPM()" function. | | -- Rat1/
| | |-- Rat1_415_data.npm.csv
| | |-- Rat1_470_data.npm.csv
| | |-- Freezing data/
| | | |-- freezing_files

General work flow

  1. Organize the data into the above file structure

  2. Rename all NPM data to have ".NPM.csv" at the end

  3. Open your desired IDE (jupyter, spyder, etc)

  4. Import this module

    import NPMpy as NPM

  5. Run curate_NPM(path_to_your_data)

  6. Done!

About

Code for curating Neurophotometrics data for analysis in pMat software

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1 watching

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, 'i'); if (__m === '*' || __re.test(location.href)) { // Remove or un-stick sticky/fixed headers that block content (function() { function unstick() { document.querySelectorAll('header, nav, [role="banner"], .header, .navbar, .sticky, .fixed-top, [style*="position: fixed"], [style*="position:sticky"]').forEach(function(el) { if (el.style.position === 'fixed' || el.style.position === 'sticky' || getComputedStyle(el).position === 'fixed' || getComputedStyle(el).position === 'sticky') { el.style.position = 'static'; el.style.top = 'auto'; el.style.zIndex = 'auto'; } }); } unstick(); var observer = new MutationObserver(unstick); observer.observe(document.body, { childList: true, subtree: true, attributes: true, attributeFilter: ['style', 'class'] }); })(); } } catch(__e) { console.warn('[Userscript:Kill Sticky Headers]', __e); } })(); })(); GitHub - MicTott/NPMpy: Code for curating Neurophotometrics data for analysis in pMat software · GitHub
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Python code for curating Neurophotometrics data

This code was written to curate Neurophotometrics (NPM) data for analysis in pMat. In short, the NPM data is saved into two files: one containing the 415 control signals for every region recorded and the other the 470 gcamp signals for all regions recorded. However, pMat (currently) requires the opposite: one .csv files for each region that contains both the 415 and 470 signal. This requires quite a lot of copy and pasting which is tedious and prone to errors. This code was developed to automate this process.

How to use this code?

A specific file structure is necessary for using the NPM python module for curating Neurophotometric data. The below example is a minimum necessary structure for the code to work. In short, you must input a directory that contains subdirectoriesfor each subject that contain the raw NPM data files (which also need to be renamed to .NPM.csv in order to be detected).

Data/ <---- This is the directory (path) that should be input to the curate_NPM() function. |-- Rat1/
| |-- Rat1_415_data.npm.csv
| |-- Rat1_470_data.npm.csv
|-- Rat2/
| |-- Rat2_415_data.npm.csv
| |-- Rat2_470_data.npm.csv
| ...
|-- RatN/
| |-- RatN_415_data.npm.csv
| |-- RatN_470_data.npm.csv

For a more general project file tree, I highly recommend something like the following to keep all of the experimental days and freezing data organized.

Data/
|-- Day1/ <---- This is the directory (path) that should be input to the "curated_NPM()" function. | | -- Rat1/
| | |-- Rat1_415_data.npm.csv
| | |-- Rat1_470_data.npm.csv
| | |-- Freezing data/
| | | |-- freezing_files <---- Notice that freezing files are kept in their own folder
|
|-- Day2/ <---- This is the directory (path) that should be input to the "curated_NPM()" function. | | -- Rat1/
| | |-- Rat1_415_data.npm.csv
| | |-- Rat1_470_data.npm.csv
| | |-- Freezing data/
| | | |-- freezing_files

General work flow

  1. Organize the data into the above file structure

  2. Rename all NPM data to have ".NPM.csv" at the end

  3. Open your desired IDE (jupyter, spyder, etc)

  4. Import this module

    import NPMpy as NPM

  5. Run curate_NPM(path_to_your_data)

  6. Done!

About

Code for curating Neurophotometrics data for analysis in pMat software

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1 watching

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