Oxytocin neurons signal state-dependent transitions from rest to thermogenesis and behavioral arousal.
The 7 matches
- [1] § Materials and methods › Computer vision analysis › SGBS for thermographic temperature extraction ↔ src/utils/utils.py, lines 204 to 301 · score 0.79 · predicted box, bounding box, predicted mask, temperature statistics, class, min · Report a mismatch
- [2] § Materials and methods › Fiber photometry recordings › Calcium data preprocessing ↔ Code/NP_processed_homecage_v8_lactation.R, lines 1196 to 1248 · score 0.79 · baseline subtracted, half max, pre peak, peak normalized, trace, window · Report a mismatch
- [3] § Materials and methods › Computer vision analysis › SGBS for thermographic temperature extraction ↔ src/data/Data_alignment.py, lines 368 to 446 · score 0.69 · ground truth, bounding box, skeleton, mapped, min, training · Report a mismatch
- [4] § Materials and methods › Computer vision analysis › SGBS for thermographic temperature extraction ↔ src/models/SG_MaskRCNN_train.py, lines 85 to 118 · score 0.68 · CNN model, custom Mask, network, trained, channels, skeleton · Report a mismatch
- [5] § Results › PVNOT peaks signal increases in BAT thermogenesis and changes in regional surface temperature ↔ src/models/SG_MaskRCNN_train.py, lines 85 to 118 · score 0.63 · attention layer, skeleton guided, network, CNN, trained, keypoints · Report a mismatch
- [6] § Results › PVNOT Ca2+ peaks track rest and arousal behavior states in social and non-social conditions ↔ Code/NP_processed_homecage_v8.R, lines 1967 to 2045 · score 0.57 · bout duration, bout length, active huddling, ambient, nesting, solo · Report a mismatch
- [7] § Materials and methods › Statistics › Effect of optogenetic stimulation on thermal profile ↔ Code/Opto_processed_v3.R, lines 624 to 673 · score 0.54 · LightOn, core Tb, mouse ID, bins, stimulus, 60 s · Report a mismatch
Paper
Loaded from Europe PMC by your browser; OSCR does not store it: doi.org · Europe PMC
The paper is loaded when this pane is shown.
The authors' code
Python · 240 lines · 10 KB · MIT · 2 matches
- import os
- import torch
- import torch.nn as nn
- import torchvision
- import json
- from torchvision.models import resnet50, ResNet50_Weights
- from torchvision.models.detection import MaskRCNN
- from torchvision.models.detection.rpn import AnchorGenerator
- from src.data.Data_alignment import prepare_dataloader
- from src.utils.utils import keypoints_to_heatmaps, visualize_prediction_images, filter_duplicate_classes
- import csv
- os.environ["KMP_DUPLICATE_LIB_OK"] = "TRUE" # Ignore
- # Define directories
- csv_directory = r'F:\DLC_thermography-JLanden-2024-07-09\videos' #Keypoints from DLC
- image_directory = r'F:\DLC_thermography-JLanden-2024-07-09\labeled-data' # Images
- segments_dirs = r'F:\Segmentation\training_segments' # Training segments from Darwin
- save_to_dir = r'F:\Segmentation\compare_02-13-25_BS8_check' #Where output is saved
- # Parameters
- num_epochs = 200
- validate_every_n_epochs = 200
- batch_size = 8 # Adjust as needed
- val_split = 0.2 # 20% of the data for validation
- #mask_threshold = 0.5 # 0.5 is normal
- mask_display_threshold = 0.9
- save_weights = False
- save_losses = True
- image_size = (348, 464) # H, W
- num_keypoints = 19
- num_classes = 4 # Set this according to your dataset (# classes + background)
- class_names = ['background', 'implanted_mouse', 'implanted_bat', 'implanted_rump' #,
- # , 'extra_mouse', 'extra_bat', 'extra_rump'
- ]
- loss_history = [] # Store loss values for CSV
- colors = [(1, 0, 0), (.1, .6, .1), (0, 0, 1)] #R, G, B: Must match number of class names
- # Attention Mechanism
- class AttentionLayer(nn.Module):
- def __init__(self, img_channels, keypoint_channels, attention_channels):
- super(AttentionLayer, self).__init__()
- # Convolution layers for image and keypoints (input)
- self.img_conv1 = nn.Conv2d(img_channels, attention_channels, kernel_size=1)
- self.img_conv2 = nn.Conv2d(attention_channels, attention_channels, kernel_size=3, padding=1)
- self.img_conv3 = nn.Conv2d(attention_channels, attention_channels, kernel_size=3, padding=1)
- self.keypoint_conv1 = nn.Conv2d(keypoint_channels, attention_channels, kernel_size=1)
- self.keypoint_conv2 = nn.Conv2d(attention_channels, attention_channels, kernel_size=3, padding=1)
- self.keypoint_conv3 = nn.Conv2d(attention_channels, attention_channels, kernel_size=3, padding=1)
- # Activation function
- self.relu = nn.ReLU()
- # Convolution for the attention mechanism (combine image and keypoint features)
- self.attention_conv1 = nn.Conv2d(attention_channels, attention_channels, kernel_size=3, padding=1)
- self.attention_conv2 = nn.Conv2d(attention_channels, attention_channels, kernel_size=3, padding=1)
- self.sigmoid = nn.Sigmoid()
- def forward(self, images, keypoints):
- # Process the image through multiple convolutions
- img_out = self.relu(self.img_conv1(images))
- img_out = self.relu(self.img_conv2(img_out))
- img_out = self.relu(self.img_conv3(img_out))
- # Process the keypoints through multiple convolutions
- keypoint_out = self.relu(self.keypoint_conv1(keypoints))
- keypoint_out = self.relu(self.keypoint_conv2(keypoint_out))
- keypoint_out = self.relu(self.keypoint_conv3(keypoint_out))
- # Combine image and keypoint features using element-wise multiplication
- combined = img_out * keypoint_out
- # Apply further attention convolutions
- attention_map = self.relu(self.attention_conv1(combined))
- attention_map = self.sigmoid(self.attention_conv2(attention_map))
- # Apply attention to image features
- enhanced_img_features = images * attention_map
- return enhanced_img_features
- # Custom Mask R-CNN Model with Attention
- class SkeletonGuidedMaskRCNN(nn.Module):
- def __init__(self, num_classes):
- super(SkeletonGuidedMaskRCNN, self).__init__()
- # Attention layer first to overlay images with keypoints
- self.attention = AttentionLayer(img_channels=3, keypoint_channels=num_keypoints, attention_channels=3)
- # Load a pre-trained Mask R-CNN backbone
- backbone = resnet50(weights=ResNet50_Weights.IMAGENET1K_V2)
- backbone = nn.Sequential(*list(backbone.children())[:-2]) # Remove last fully connected layer
- self.backbone = backbone
- self.backbone.out_channels = 2048
- # Create an Anchor Generator for the FPN (feature pyramid network)
- anchor_generator = AnchorGenerator(sizes=((32, 64, 128, 256, 512),), aspect_ratios=((0.5, 1.0, 2.0),) * 5)
- # Define RoI Align and FPN
- roi_pooler = torchvision.ops.MultiScaleRoIAlign(featmap_names=['0'], output_size=4, sampling_ratio=2)
- # Define Mask R-CNN model with the modified backbone
- self.model = MaskRCNN(self.backbone, num_classes=num_classes, rpn_anchor_generator=anchor_generator,
- box_roi_pool=roi_pooler, mask_roi_pool=roi_pooler)
- def forward(self, images, keypoints, targets=None, return_predictions=False):
- # Apply attention to images using keypoints
- enhanced_img_features = self.attention(images, keypoints)
- # Use enhanced image features in the Mask R-CNN model
- if self.training and not return_predictions:
- return self.model(enhanced_img_features, targets)
- else: # Validate
- return self.model(enhanced_img_features)
- # Training script
- # Initialize the custom loss
- # loss_fn = CustomLoss()
- ########################
- def save_predictions_to_json(predictions, save_to_dir, videoID, frameID):
- os.makedirs(f"{save_to_dir}/predictions/{videoID}", exist_ok=True)
- json_path = os.path.join(save_to_dir, f"predictions", videoID, f"predictions_{frameID}.txt")
- serializable_predictions = []
- for pred in predictions:
- serializable_predictions.append({
- 'labels': pred['labels'].cpu().tolist(), # Convert tensor to list
- 'scores': pred['scores'].cpu().tolist(), # Convert tensor to list
- 'boxes': pred['boxes'].cpu().tolist(), # Convert tensor to list
- 'masks': pred['masks'].cpu().numpy().tolist() # Convert tensor to nested lists
- })
- # Write the predictions to a file in JSON format
- with open(json_path, 'w') as f:
- json.dump(serializable_predictions, f, indent=4)
- #####################
- def train_model(train_loader, val_loader, num_classes, num_epochs=num_epochs):
- device = torch.device("cuda") if torch.cuda.is_available() else torch.device("cpu")
- model = SkeletonGuidedMaskRCNN(num_classes=num_classes).to(device)
- optimizer = torch.optim.Adam(model.parameters(), lr=1e-4)
- for epoch in range(num_epochs):
- model.train()
- total_loss = 0
- for batch_idx, (images, segments, skeletons) in enumerate(train_loader):
- images = [image.to(device) for image in images]
- H, W = images[0].shape[1], images[0].shape[2]
- # Convert images to tensors
- images = torch.stack([image.to(device) for image in images]).to(device)
- keypoints = skeletons.to(device)
- kp_heatmaps = keypoints_to_heatmaps(keypoints, H, W)
- segments = [{k: (v.to(device) if isinstance(v, torch.Tensor) else v) for k, v in segment.items()} for
- segment in segments]
- optimizer.zero_grad()
- outputs = model(images, kp_heatmaps, segments)
- # Use the losses from the model's output
- rcnn_losses = sum(loss for loss in outputs.values())
- total_loss = rcnn_losses
- total_loss.backward()
- optimizer.step()
- total_loss += total_loss.item()
- avg_loss = total_loss / len(train_loader)
- print(f"Epoch [{epoch + 1}/{num_epochs}], Loss: {avg_loss}")
- # Store loss history for CSV
- loss_history.append([epoch + 1, avg_loss.item()])
- if (epoch + 1) % validate_every_n_epochs == 0:
- model.eval()
- predictions_list = []
- for batch_idx, (images, segments, skeletons) in enumerate(val_loader):
- images = [image.to(device) for image in images]
- H, W = images[0].shape[1], images[0].shape[2]
- images = torch.stack([image.to(device) for image in images]).to(device)
- keypoints = skeletons.to(device)
- kp_heatmaps = keypoints_to_heatmaps(keypoints, H, W)
- segments = [{k: (v.to(device) if isinstance(v, torch.Tensor) else v) for k, v in segment.items()} for
- segment in segments]
- with torch.no_grad(): # Disable gradient calculation
- # Get predictions instead of losses
- predictions = model(images, kp_heatmaps)
- predictions = filter_duplicate_classes(predictions)
- predictions_list.append(predictions)
- # Optionally visualize here
- visualize_prediction_images(
- images=images,
- predictions=predictions,
- epoch=epoch + 1,
- phase="validate",
- batch_idx=batch_idx,
- save_img_dir=save_to_dir,
- class_names=class_names,
- colors=colors,
- keypoints=keypoints,
- threshold=mask_display_threshold
- )
- else:
- continue
- # Save model weights
- if save_weights is True:
- model_save_path = os.path.join(save_to_dir, f'sg-mrcnn_epochs_{num_epochs}.pth')
- torch.save(model.state_dict(), model_save_path)
- print(f"Model weights saved to {model_save_path}")
- if save_losses is True:
- loss_csv_path = os.path.join(save_to_dir, f"main_loss_{num_epochs}.csv")
- # Save loss history to CSV
- with open(loss_csv_path, mode="w", newline="") as file:
- writer = csv.writer(file)
- writer.writerow(["Epoch", "Loss"]) # Write header
- writer.writerows(loss_history) # Write epoch, loss pairs
- return model
- if __name__ == "__main__":
- # Assuming train_loader and val_loader are already created with your data
- train_loader, val_loader = prepare_dataloader(csv_directory, segments_dirs, image_directory,
- batch_size, val_split) # Implement this function
- trained_model = train_model(train_loader, val_loader, num_classes)
SG_MaskRCNN_train.py at commit 06d57d8, under MIT · at the source
Overview
- Department of Zoology and Physiology, University of Wyoming, Laramie, United States
- Department of Biological Sciences, Brock University, St. Catherines, Canada
Abstract
Core body temperature (Tb) is defended within narrow limits through thermoregulatory behaviors like huddling, nesting, and physical activity, as well as autonomic responses like brown fat thermogenesis. While Tb displays regulated fluctuations across different behavioral states and rest/
Reproduced under the paper's license (CC BY), from the paper cited above.
Repositories
Its files are read in the Code ↔ Paper reader above, with 7 matches between paragraphs and lines of code.
Zenodo 2652896
Availability: 1 check, the latest on 31 October 2026: the link answers (HTTP 200)
- 31 October 2026: the link answers (HTTP 200)
3 files
- scripts/
split.pl , Perl, 107 lines - LICENSE.md, License, 40 lines
- Readme.md, Text, 332 lines
j-landen/seq_process
90225182607b2faa19f9dacb0252430df0e7d598, 28 October 2026Availability: 1 check, the latest on 31 October 2026: the link answers
- 31 October 2026: the link answers
3 files
- Seq_process.py, Python, 276 lines
- LICENSE, License, 21 lines
- README.md, Text, 56 lines
j-landen/SGBS
06d57d84fa17d1db45ecec70b686c2c0761716f9, 28 October 2026Availability: 1 check, the latest on 31 October 2026: the link answers
- 31 October 2026: the link answers
8 files
- src/
data/ , Python, 65 linesDLC_Skeleton_tracking.py - src/
data/ , Python, 536 lines, 1 matchData_alignment.py - src/
models/ , Python, 157 linesSG_MaskRCNN_analysis.py - src/
models/ , Python, 240 lines, 2 matchesSG_MaskRCNN_train.py - src/
utils/ , Python, 301 lines, 1 matchutils.py - src/
utils/ , Python, 150 linesvisualize_copy.py - LICENSE, License, 27 lines
- readme.md, Text, 120 lines
OSF x9kcj
Availability: 1 check, the latest on 31 October 2026: the link answers (HTTP 200)
- 31 October 2026: the link answers (HTTP 200)
4 files
- Code/
NP_processed_homecage_v8 , R, 2,898 lines, 1 match.R - Code/
NP_processed_homecage_v8 , R, 1,374 lines, 1 match_lactation.R - Code/
Opto_processed_v3.R , R, 1,853 lines, 1 match - README.txt, Text, 48 lines
gtatters/thermimagej
cb82c240d409700460cdbb89df104aa104df18d8, 27 June 2026Availability: 1 check, the latest on 31 October 2026: the link answers
- 31 October 2026: the link answers
6 files
- scripts/
ats-repair.pl , Perl, 379 lines - scripts/
ats-split.pl , Perl, 679 lines - scripts/
ats-xml.pl , Perl, 1,125 lines - scripts/
split.pl , Perl, 154 lines - LICENSE.md, License, 40 lines
- Readme.md, Text, 703 lines
The paper's code and data availability statement is in the Data section.
Tracing map
Proposed by the machine: these links were found in the paper and verified at the source, without human review. The map will receive a Zenodo DOI once one of the paper's authors has validated it with their ORCID.
What the map holds:
- 5 repositories of the authors' code, each at its verified commit, with its license and how the link was found in the paper;
- 15 scripts, each with its path and the digest of its content;
- 7 matches between paragraphs of the paper and lines of the code (method lexical-v1);
- neither the text of the paper nor the code itself.
Its JSON (tracing-map.json) is deposited on Zenodo with its DOI once the map is validated.
Data
No dataset and no data link were found in the paper.
Data availability
Data and code underlying this study are publicly available via the Open Science Framework (OSF) at https://
The following dataset was generated:
Nelson A. 2025. Oxytocin Neurons Signal State-Dependent Transitions From Rest To Thermogenesis And Behavioral Arousal. Open Science Framework. x9kcj
Reproduced under the paper's license (CC BY), from the paper cited above.
Versions
The history of this record: each version stored by the harvester or made by a correction of its authors or of the maintainers of its code, and what changed in its facts. The texts of the paper (its abstract, its availability statements) are not part of it; versions that changed only those are not listed.
Version 1, 31 October 2026: the first record
Recorded: type, language, journal, volume, pages, dates, 9 authors, 1 keyword, 11 MeSH terms, 2 funders, 98 references, 7 RRIDs.
Cite
This paper
Vandendoren, M., Landen, J. G., Rogers, J. F., Killmer, S., Alamiri, B., Pohlman, C., Tattersall, G., Bedford, N. L., & Nelson, A. (2026). Oxytocin neurons signal state-dependent transitions from rest to thermogenesis and behavioral arousal. eLife, 14, RP108212. https://
BibTeX
@article{vandendoren2026
author = {Vandendoren, Morgane and Landen, Jason G and Rogers, Joseph F and Killmer, Samantha and Alamiri, Baizar and Pohlman, Celeste and Tattersall, Glenn and Bedford, Nicole L and Nelson, Adam},
title = {{Oxytocin neurons signal state-dependent transitions from rest to thermogenesis and behavioral arousal}},
journal = {eLife},
year = {2026},
month = oct,
volume = {14},
pages = {RP108212},
publisher = {eLife Sciences Publications, Ltd},
issn = {2050-084X},
doi = {10.7554/
url = {https://
pmid = {42960829},
pmcid = {PMC13722414}
}
RIS
TY - JOUR
AU - Vandendoren, Morgane
AU - Landen, Jason G
AU - Rogers, Joseph F
AU - Killmer, Samantha
AU - Alamiri, Baizar
AU - Pohlman, Celeste
AU - Tattersall, Glenn
AU - Bedford, Nicole L
AU - Nelson, Adam
TI - Oxytocin neurons signal state-dependent transitions from rest to thermogenesis and behavioral arousal
T2 - eLife
J2 - eLife
PY - 2026
DA - 2026/
VL - 14
SP - RP108212
SN - 2050-084X
PB - eLife Sciences Publications, Ltd
DO - 10.7554/
UR - https://
LA - en
ER -
CSL-JSON
{
"id": "10.7554/
"type": "article-journal",
"title": "Oxytocin neurons signal state-dependent transitions from rest to thermogenesis and behavioral arousal",
"container-title": "eLife",
"author": [
{
"family": "Vandendoren",
"given": "Morgane"
},
{
"family": "Landen",
"given": "Jason G"
},
{
"family": "Rogers",
"given": "Joseph F"
},
{
"family": "Killmer",
"given": "Samantha"
},
{
"family": "Alamiri",
"given": "Baizar"
},
{
"family": "Pohlman",
"given": "Celeste"
},
{
"family": "Tattersall",
"given": "Glenn"
},
{
"family": "Bedford",
"given": "Nicole L"
},
{
"family": "Nelson",
"given": "Adam"
}
],
"container-title-short":
"volume": "14",
"page": "RP108212",
"DOI": "10.7554/
"PMID": "42960829",
"PMCID": "PMC13722414",
"ISSN": "2050-084X",
"publisher": "eLife Sciences Publications, Ltd",
"URL": "https://
"language": "en",
"issued": {
"date-parts": [
[
2026,
10,
30
]
]
}
}
The tracing map gets a citation of its own once an author has validated it and it has a DOI.
Similar papers
The papers with a page that share the most with this one: the tools found in their code, their categories, datasets, cited references and authors, the rarest counting most.
- [1] doi:10.1093/braincomms/fcaf432 [code]
- The effect of chronic stress and chronic alcohol intake on behaviour, brain volume, and functional connectivity in a longitudinal rat model.Journal: Brain communicationsIn common: DeepLabCut, multcomp, broom, 10 other tools
- [2] doi:10.1093/bioinformatics/btag592 [code]
- Network-based stratification of allele-specific expression reveals patient subgroups in Huntington's disease.Journal: Bioinformatics (Oxford, England)In common: multcomp, pROC, broom, 11 other tools
- [3] doi:10.1038/s41467-026-70832-2 [code]
- Characterizing spatiotemporal white matter hyperintensity pathophysiology in vivo to disentangle vascular and neurodegenerative contributions.Journal: Nature communicationsIn common: multcomp, broom, emmeans, 11 other tools
- [4] doi:10.1186/s11689-025-09651-3 [code]
- The association between infant EEG aperiodic exponent and the trajectory of restricted and repetitive behaviors for toddlers with and without autism.Journal: Journal of neurodevelopmental disordersIn common: multcomp, broom, emmeans, 11 other tools
- [5] doi:10.1038/s41586-022-05562-8 [code]
- Synaptic gradients transform object location to action.Journal: NatureIn common: DeepLabCut, imageio, Plotly, 11 other tools
- [6] doi:10.1038/s41586-025-08840-3 [code]
- Functional connectomics reveals general wiring rule in mouse visual cortex.Journal: NatureIn common: DeepLabCut, imageio, broom, 9 other tools, mouse, 1 reference
- [7] doi:10.1016/j.celrep.2026.117646 [code]
- Medial entorhinal-hippocampal desynchronization parallels the emergence of memory impairment in a mouse model of Alzheimer's disease pathology.Journal: Cell reportsIn common: multcomp, broom, emmeans, 9 other tools, mouse
- [8] doi:10.1038/s41467-026-70639-1 [code]
- Anterior cingulate neurons combine outcome monitoring of past decisions with ongoing movement signals.Journal: Nature communicationsIn common: DeepLabCut, emmeans, lmerTest, 8 other tools, mouse, 1 reference
- [9] doi:10.1016/j.xcrm.2026.102682 [code]
- TET CpG sequence-context-specifi
c DNA demethylation shapes progression of IDH-mutant gliomas. Journal: Cell reports. MedicineIn common: multcomp, pROC, broom, 8 other tools - [10] doi:10.1016/j.celrep.2023.113305 [code]
- High-calorie diets uncouple hypothalamic oxytocin neurons from a gut-to-brain satiation pathway via κ-opioid signaling.Journal: Cell reportsIn common: ggplot2, tidyverse, pandas, 2 other tools, mouse, 6 references
Contribute
The authors of this paper can claim it, correct its record and validate its tracing map, and the maintainers of its code (its owner, or a public member of its organization) correct what it says of their repository; anyone signed in can ask for its removal. Every request goes to OSCR's own machine, which answers it; your account page follows them.
Sign in with ORCID to claim this paper as one of its authors, correct its record or validate its tracing map: when the paper's metadata lists your ORCID iD, you are recognized at once. Maintainers of its code: sign in with GitHub, then claim the repository on your account page.
Claim this paper
Correct its record
Say what each link of this record is, remove the ones that are not the paper's, add the ones that are missing. The correction becomes a new version of the record, in its Versions section.
Validate its tracing map
You validate the map as this page shows it: 5 repositories of the authors' code, each at its verified commit and with its license, 15 scripts, and 7 matches between paragraphs and code (see the Code and Map sections). It then receives a DOI on Zenodo, with you (your ORCID iD) and OSCR as its creators; the code itself is not deposited.
The map's fingerprint: sha256:97397a0b9c088fe9…
Add the badge to the code's README
If you are an author or a maintainer of this paper's code, you can add this badge. It says what OSCR knows of the paper (its code, its validated tracing map) and links the code to this page. Paste one of these snippets under the README's title. Keep the two marks around it, so that the badge can be replaced in place and is never added twice. OSCR changes nothing in your repository.
Markdown
<!-- oscr-badge:start -->
[](https://openscicode.org/badge/doi/10.7554/elife.108212)
<!-- oscr-badge:end -->reStructuredText
.. oscr-badge:start
.. image:: https://openscicode.org/badge/doi/10.7554/elife.108212.svg
:target: https://openscicode.org/badge/doi/10.7554/elife.108212
:alt: OSCR
.. oscr-badge:endHTML
<!-- oscr-badge:start -->
<a href="https://openscicode.org/badge/doi/10.7554/elife.108212"><img src="https://openscicode.org/badge/doi/10.7554/elife.108212.svg" alt="OSCR"></a>
<!-- oscr-badge:end -->On GitHub, open the README, choose Edit (the pencil), paste the snippet under the title, then "Commit changes".
- j-landen/seq_process: README.md on GitHub
- j-landen/SGBS: readme.md on GitHub
- gtatters/thermimagej: Readme.md on GitHub
If you choose to, you can have the badge kept up to date for you, with oscr badge --write from the command line or with the GitHub Action in your repository's workflows. Every other form and option (a card, AsciiDoc, LaTeX, shields.io) is on the badge page.
Request its removal
To ask OSCR to remove this record, the copies of its authors' scripts or its tracing map, use the removal request page: signed in, you say who you are, what to remove and why, then review and confirm the request. Published rules decide every request (how).
Discussion, reproductions, activity
Discussion: code errors and mismatches between the code and the paper about this paper and its code, from readers and its authors, beside the paper and its tracing map.
Report a mismatch between the code and the paper · Report a code error (signed in)
Reproductions: reports from readers who ran the authors' code and did not get the paper's result, what they ran, with which environment, commit and data.
Report a reproduction failure (signed in)
Versions of its code: the releases of its code tied to a version of this paper (the preprint, the accepted manuscript, the version of record…), each with the tracing map versioned with it.
Activity: what happens around this paper: new versions of its record, its map's validation, discussions and reproductions. It opens with sign-in.
