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Title: Data from: Parallel processing in speech perception with local and global representations of linguistic context
Speech processing is highly incremental. It is widely accepted that human listeners continuously use the linguistic context to anticipate upcoming concepts, words, and phonemes. However, previous evidence supports two seemingly contradictory models of how a predictive context is integrated with the bottom-up sensory input: Classic psycholinguistic paradigms suggest a two-stage process, in which acoustic input initially leads to local, context-independent representations, which are then quickly integrated with contextual constraints. This contrasts with the view that the brain constructs a single coherent, unified interpretation of the input, which fully integrates available information across representational hierarchies, and thus uses contextual constraints to modulate even the earliest sensory representations. To distinguish these hypotheses, we tested magnetoencephalography responses to continuous narrative speech for signatures of local and unified predictive models. Results provide evidence that listeners employ both types of models in parallel. Two local context models uniquely predict some part of early neural responses, one based on sublexical phoneme sequences, and one based on the phonemes in the current word alone; at the same time, even early responses to phonemes also reflect a unified model that incorporates sentence-level constraints to predict upcoming phonemes. Neural source localization places the anatomical origins of the different predictive models in nonidentical parts of the superior temporal lobes bilaterally, with the right hemisphere showing a relative preference for more local models. These results suggest that speech processing recruits both local and unified predictive models in parallel, reconciling previous disparate findings. Parallel models might make the perceptual system more robust, facilitate processing of unexpected inputs, and serve a function in language acquisition. MEG Data MEG data is in FIFF format and can be opened with MNE-Python. Data has been directly converted from the acquisition device native format without any preprocessing. Events contained in the data indicate the stimuli in numerical order. Subjects R2650 and R2652 heard stimulus 11b instead of 11. Predictor Variables The original audio files are copyrighted and cannot be shared, but the make_audio folder contains make_clips.py which can be used to extract the exact clips from the commercially available audiobook (ISBN 978-1480555280). The predictors directory contains all the predictors used in the original study as pickled eelbrain objects. They can be loaded in Python with the eelbrain.load.unpickle function. The TextGrids directory contains the TextGrids aligned to the audio files. Source Localization The localization.zip file contains files needed for source localization. Structural brain models used in the published analysis are reconstructed by scaling the FreeSurfer fsaverage brain (distributed with FreeSurfer) based on each subject's `MRI scaling parameters.cfg` file. This can be done using the `mne.scale_mri` function. Each subject's MEG folder contains a `subject-trans.fif` file which contains the coregistration between MEG sensor space and (scaled) MRI space, which is used to compute the forward solution.  more » « less
Award ID(s):
1734892
NSF-PAR ID:
10340192
Author(s) / Creator(s):
; ; ; ; ;
Publisher / Repository:
Dryad
Date Published:
Edition / Version:
5
Subject(s) / Keyword(s):
["FOS: Biological sciences"]
Format(s):
Medium: X Size: 25129288550 bytes
Size(s):
["25129288550 bytes"]
Sponsoring Org:
National Science Foundation
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  1. Speech processing is highly incremental. It is widely accepted that human listeners continuously use the linguistic context to anticipate upcoming concepts, words, and phonemes. However, previous evidence supports two seemingly contradictory models of how a predictive context is integrated with the bottom-up sensory input: Classic psycholinguistic paradigms suggest a two-stage process, in which acoustic input initially leads to local, context-independent representations, which are then quickly integrated with contextual constraints. This contrasts with the view that the brain constructs a single coherent, unified interpretation of the input, which fully integrates available information across representational hierarchies, and thus uses contextual constraints to modulate even the earliest sensory representations. To distinguish these hypotheses, we tested magnetoencephalography responses to continuous narrative speech for signatures of local and unified predictive models. Results provide evidence that listeners employ both types of models in parallel. Two local context models uniquely predict some part of early neural responses, one based on sublexical phoneme sequences, and one based on the phonemes in the current word alone; at the same time, even early responses to phonemes also reflect a unified model that incorporates sentence-level constraints to predict upcoming phonemes. Neural source localization places the anatomical origins of the different predictive models in nonidentical parts of the superior temporal lobes bilaterally, with the right hemisphere showing a relative preference for more local models. These results suggest that speech processing recruits both local and unified predictive models in parallel, reconciling previous disparate findings. Parallel models might make the perceptual system more robust, facilitate processing of unexpected inputs, and serve a function in language acquisition. 
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  2. Data files were used in support of the research paper titled “Mitigating RF Jamming Attacks at the Physical Layer with Machine Learning" which has been submitted to the IET Communications journal.

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    All data was collected using the SDR implementation shown here: https://github.com/mainland/dragonradio/tree/iet-paper. Particularly for antenna state selection, the files developed for this paper are located in 'dragonradio/scripts/:'

    • 'ModeSelect.py': class used to defined the antenna state selection algorithm
    • 'standalone-radio.py': SDR implementation for normal radio operation with reconfigurable antenna
    • 'standalone-radio-tuning.py': SDR implementation for hyperparameter tunning
    • 'standalone-radio-onmi.py': SDR implementation for omnidirectional mode only

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    Authors: Marko Jacovic, Xaime Rivas Rey, Geoffrey Mainland, Kapil R. Dandekar
    Contact: krd26@drexel.edu

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    Top-level directories and content will be described below. Detailed descriptions of experiments performed are provided in the paper.

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    classifier_training: files used for training classifiers that are integrated into SDR platform

    • 'logs-8-18' directory contains OTA SDR collected log files for each jammer type and under normal operation (including congested and weaklink states)
    • 'classTrain.py' is the main parser for training the classifiers
    • 'trainedClassifiers' contains the output classifiers generated by 'classTrain.py'

    post_processing_classifier: contains logs of online classifier outputs and processing script

    • 'class' directory contains .csv logs of each RTE and OTA experiment for each jamming and operation scenario
    • 'classProcess.py' parses the log files and provides classification report and confusion matrix for each multi-class and binary classifiers for each observed scenario - found in 'results->classifier_performance'

    post_processing_mgen: contains MGEN receiver logs and parser

    • 'configs' contains JSON files to be used with parser for each experiment
    • 'mgenLogs' contains MGEN receiver logs for each OTA and RTE experiment described. Within each experiment logs are separated by 'mit' for mitigation used, 'nj' for no jammer, and 'noMit' for no mitigation technique used. File names take the form *_cj_* for constant jammer, *_pj_* for periodic jammer, *_rj_* for reactive jammer, and *_nj_* for no jammer. Performance figures are found in 'results->mitigation_performance'

    ray_tracing_emulation: contains files related to Drexel area, Art Museum, and UAV Drexel area validation RTE studies.

    • Directory contains detailed 'readme.txt' for understanding.
    • Please note: the processing files and data logs present in 'validation' folder were developed by Wolfe et al. and should be cited as such, unless explicitly stated differently. 
      • S. Wolfe, S. Begashaw, Y. Liu and K. R. Dandekar, "Adaptive Link Optimization for 802.11 UAV Uplink Using a Reconfigurable Antenna," MILCOM 2018 - 2018 IEEE Military Communications Conference (MILCOM), 2018, pp. 1-6, doi: 10.1109/MILCOM.2018.8599696.

    results: contains results obtained from study

    • 'classifier_performance' contains .txt files summarizing binary and multi-class performance of online SDR system. Files obtained using 'post_processing_classifier.'
    • 'mitigation_performance' contains figures generated by 'post_processing_mgen.'
    • 'validation' contains RTE and OTA performance comparison obtained by 'ray_tracing_emulation->validation->matlab->outdoor_hover_plots.m'

    tuning_parameter_study: contains the OTA log files for antenna state selection hyperparameter study

    • 'dataCollect' contains a folder for each jammer considered in the study, and inside each folder there is a CSV file corresponding to a different configuration of the learning parameters of the reconfigurable antenna. The configuration selected was the one that performed the best across all these experiments and is described in the paper.
    • 'data_summary.txt'this file contains the summaries from all the CSV files for convenience.
     
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  3. Data files were used in support of the research paper titled "“Experimentation Framework for Wireless
    Communication Systems under Jamming Scenarios" which has been submitted to the IET Cyber-Physical Systems: Theory & Applications journal. 

    Authors: Marko Jacovic, Michael J. Liston, Vasil Pano, Geoffrey Mainland, Kapil R. Dandekar
    Contact: krd26@drexel.edu

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    Top-level directories correspond to the case studies discussed in the paper. Each includes the sub-directories: logs, parsers, rayTracingEmulation, results. 

    --------------------------------

    logs:    - data logs collected from devices under test
        - 'defenseInfrastucture' contains console output from a WARP 802.11 reference design network. Filename structure follows '*x*dB_*y*.txt' in which *x* is the reactive jamming power level and *y* is the jaming duration in samples (100k samples = 1 ms). 'noJammer.txt' does not include the jammer and is a base-line case. 'outMedian.txt' contains the median statistics for log files collected prior to the inclusion of the calculation in the processing script. 
        - 'uavCommunication' contains MGEN logs at each receiver for cases using omni-directional and RALA antennas with a 10 dB constant jammer and without the jammer. Omni-directional folder contains multiple repeated experiments to provide reliable results during each calculation window. RALA directories use s*N* folders in which *N* represents each antenna state. 
        - 'vehicularTechnologies' contains MGEN logs at the car receiver for different scenarios. 'rxNj_5rep.drc' does not consider jammers present, 'rx33J_5rep.drc' introduces the periodic jammer, in 'rx33jSched_5rep.drc' the device under test uses time scheduling around the periodic jammer, in 'rx33JSchedRandom_5rep.drc' the same modified time schedule is used with a random jammer. 

    --------------------------------

    parsers:    - scripts used to collect or process the log files used in the study
            - 'defenseInfrastructure' contains the 'xputFiveNodes.py' script which is used to control and log the throughput of a 5-node WARP 802.11 reference design network. Log files are manually inspected to generate results (end of log file provides a summary). 
            - 'uavCommunication' contains a 'readMe.txt' file which describes the parsing of the MGEN logs using TRPR. TRPR must be installed to run the scripts and directory locations must be updated. 
            - 'vehicularTechnologies' contains the 'mgenParser.py' script and supporting 'bfb.json' configuration file which also require TRPR to be installed and directories to be updated. 

    --------------------------------

    rayTracingEmulation:    - 'wirelessInsiteImages': images of model used in Wireless Insite
                - 'channelSummary.pdf': summary of channel statistics from ray-tracing study
                - 'rawScenario': scenario files resulting from code base directly from ray-tracing output based on configuration defined by '*WI.json' file 
                - 'processedScenario': pre-processed scenario file to be used by DYSE channel emulator based on configuration defined by '*DYSE.json' file, applies fixed attenuation measured externally by spectrum analyzer and additional transmit power per node if desired
                - DYSE scenario file format: time stamp (milli seconds), receiver ID, transmitter ID, main path gain (dB), main path phase (radians), main path delay (micro seconds), Doppler shift (Hz), multipath 1 gain (dB), multipath 1 phase (radians), multipath 1 delay relative to main path delay (micro seconds), multipath 2 gain (dB), multipath 2 phase (radians), multipath 2 delay relative to main path delay (micro seconds)
                - 'nodeMapping.txt': mapping of Wireless Insite transceivers to DYSE channel emulator physical connections required
                - 'uavCommunication' directory additionally includes 'antennaPattern' which contains the RALA pattern data for the omni-directional mode ('omni.csv') and directional state ('90.csv')

    --------------------------------

    results:    - contains performance results used in paper based on parsing of aforementioned log files
     

     
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  4. Obeid, I. (Ed.)
    The Neural Engineering Data Consortium (NEDC) is developing the Temple University Digital Pathology Corpus (TUDP), an open source database of high-resolution images from scanned pathology samples [1], as part of its National Science Foundation-funded Major Research Instrumentation grant titled “MRI: High Performance Digital Pathology Using Big Data and Machine Learning” [2]. The long-term goal of this project is to release one million images. We have currently scanned over 100,000 images and are in the process of annotating breast tissue data for our first official corpus release, v1.0.0. This release contains 3,505 annotated images of breast tissue including 74 patients with cancerous diagnoses (out of a total of 296 patients). In this poster, we will present an analysis of this corpus and discuss the challenges we have faced in efficiently producing high quality annotations of breast tissue. It is well known that state of the art algorithms in machine learning require vast amounts of data. Fields such as speech recognition [3], image recognition [4] and text processing [5] are able to deliver impressive performance with complex deep learning models because they have developed large corpora to support training of extremely high-dimensional models (e.g., billions of parameters). Other fields that do not have access to such data resources must rely on techniques in which existing models can be adapted to new datasets [6]. A preliminary version of this breast corpus release was tested in a pilot study using a baseline machine learning system, ResNet18 [7], that leverages several open-source Python tools. The pilot corpus was divided into three sets: train, development, and evaluation. Portions of these slides were manually annotated [1] using the nine labels in Table 1 [8] to identify five to ten examples of pathological features on each slide. Not every pathological feature is annotated, meaning excluded areas can include focuses particular to these labels that are not used for training. A summary of the number of patches within each label is given in Table 2. To maintain a balanced training set, 1,000 patches of each label were used to train the machine learning model. Throughout all sets, only annotated patches were involved in model development. The performance of this model in identifying all the patches in the evaluation set can be seen in the confusion matrix of classification accuracy in Table 3. The highest performing labels were background, 97% correct identification, and artifact, 76% correct identification. A correlation exists between labels with more than 6,000 development patches and accurate performance on the evaluation set. Additionally, these results indicated a need to further refine the annotation of invasive ductal carcinoma (“indc”), inflammation (“infl”), nonneoplastic features (“nneo”), normal (“norm”) and suspicious (“susp”). This pilot experiment motivated changes to the corpus that will be discussed in detail in this poster presentation. To increase the accuracy of the machine learning model, we modified how we addressed underperforming labels. One common source of error arose with how non-background labels were converted into patches. Large areas of background within other labels were isolated within a patch resulting in connective tissue misrepresenting a non-background label. In response, the annotation overlay margins were revised to exclude benign connective tissue in non-background labels. Corresponding patient reports and supporting immunohistochemical stains further guided annotation reviews. The microscopic diagnoses given by the primary pathologist in these reports detail the pathological findings within each tissue site, but not within each specific slide. The microscopic diagnoses informed revisions specifically targeting annotated regions classified as cancerous, ensuring that the labels “indc” and “dcis” were used only in situations where a micropathologist diagnosed it as such. Further differentiation of cancerous and precancerous labels, as well as the location of their focus on a slide, could be accomplished with supplemental immunohistochemically (IHC) stained slides. When distinguishing whether a focus is a nonneoplastic feature versus a cancerous growth, pathologists employ antigen targeting stains to the tissue in question to confirm the diagnosis. For example, a nonneoplastic feature of usual ductal hyperplasia will display diffuse staining for cytokeratin 5 (CK5) and no diffuse staining for estrogen receptor (ER), while a cancerous growth of ductal carcinoma in situ will have negative or focally positive staining for CK5 and diffuse staining for ER [9]. Many tissue samples contain cancerous and non-cancerous features with morphological overlaps that cause variability between annotators. The informative fields IHC slides provide could play an integral role in machine model pathology diagnostics. Following the revisions made on all the annotations, a second experiment was run using ResNet18. Compared to the pilot study, an increase of model prediction accuracy was seen for the labels indc, infl, nneo, norm, and null. This increase is correlated with an increase in annotated area and annotation accuracy. Model performance in identifying the suspicious label decreased by 25% due to the decrease of 57% in the total annotated area described by this label. A summary of the model performance is given in Table 4, which shows the new prediction accuracy and the absolute change in error rate compared to Table 3. The breast tissue subset we are developing includes 3,505 annotated breast pathology slides from 296 patients. The average size of a scanned SVS file is 363 MB. The annotations are stored in an XML format. A CSV version of the annotation file is also available which provides a flat, or simple, annotation that is easy for machine learning researchers to access and interface to their systems. Each patient is identified by an anonymized medical reference number. Within each patient’s directory, one or more sessions are identified, also anonymized to the first of the month in which the sample was taken. These sessions are broken into groupings of tissue taken on that date (in this case, breast tissue). A deidentified patient report stored as a flat text file is also available. Within these slides there are a total of 16,971 total annotated regions with an average of 4.84 annotations per slide. Among those annotations, 8,035 are non-cancerous (normal, background, null, and artifact,) 6,222 are carcinogenic signs (inflammation, nonneoplastic and suspicious,) and 2,714 are cancerous labels (ductal carcinoma in situ and invasive ductal carcinoma in situ.) The individual patients are split up into three sets: train, development, and evaluation. Of the 74 cancerous patients, 20 were allotted for both the development and evaluation sets, while the remain 34 were allotted for train. The remaining 222 patients were split up to preserve the overall distribution of labels within the corpus. This was done in hope of creating control sets for comparable studies. Overall, the development and evaluation sets each have 80 patients, while the training set has 136 patients. In a related component of this project, slides from the Fox Chase Cancer Center (FCCC) Biosample Repository (https://www.foxchase.org/research/facilities/genetic-research-facilities/biosample-repository -facility) are being digitized in addition to slides provided by Temple University Hospital. This data includes 18 different types of tissue including approximately 38.5% urinary tissue and 16.5% gynecological tissue. These slides and the metadata provided with them are already anonymized and include diagnoses in a spreadsheet with sample and patient ID. We plan to release over 13,000 unannotated slides from the FCCC Corpus simultaneously with v1.0.0 of TUDP. Details of this release will also be discussed in this poster. Few digitally annotated databases of pathology samples like TUDP exist due to the extensive data collection and processing required. The breast corpus subset should be released by November 2021. By December 2021 we should also release the unannotated FCCC data. We are currently annotating urinary tract data as well. We expect to release about 5,600 processed TUH slides in this subset. We have an additional 53,000 unprocessed TUH slides digitized. Corpora of this size will stimulate the development of a new generation of deep learning technology. In clinical settings where resources are limited, an assistive diagnoses model could support pathologists’ workload and even help prioritize suspected cancerous cases. ACKNOWLEDGMENTS This material is supported by the National Science Foundation under grants nos. CNS-1726188 and 1925494. Any opinions, findings, and conclusions or recommendations expressed in this material are those of the author(s) and do not necessarily reflect the views of the National Science Foundation. REFERENCES [1] N. Shawki et al., “The Temple University Digital Pathology Corpus,” in Signal Processing in Medicine and Biology: Emerging Trends in Research and Applications, 1st ed., I. Obeid, I. Selesnick, and J. Picone, Eds. New York City, New York, USA: Springer, 2020, pp. 67 104. https://www.springer.com/gp/book/9783030368432. [2] J. Picone, T. Farkas, I. Obeid, and Y. Persidsky, “MRI: High Performance Digital Pathology Using Big Data and Machine Learning.” Major Research Instrumentation (MRI), Division of Computer and Network Systems, Award No. 1726188, January 1, 2018 – December 31, 2021. https://www. isip.piconepress.com/projects/nsf_dpath/. [3] A. Gulati et al., “Conformer: Convolution-augmented Transformer for Speech Recognition,” in Proceedings of the Annual Conference of the International Speech Communication Association (INTERSPEECH), 2020, pp. 5036-5040. https://doi.org/10.21437/interspeech.2020-3015. [4] C.-J. Wu et al., “Machine Learning at Facebook: Understanding Inference at the Edge,” in Proceedings of the IEEE International Symposium on High Performance Computer Architecture (HPCA), 2019, pp. 331–344. https://ieeexplore.ieee.org/document/8675201. [5] I. Caswell and B. Liang, “Recent Advances in Google Translate,” Google AI Blog: The latest from Google Research, 2020. [Online]. Available: https://ai.googleblog.com/2020/06/recent-advances-in-google-translate.html. [Accessed: 01-Aug-2021]. [6] V. Khalkhali, N. Shawki, V. Shah, M. Golmohammadi, I. Obeid, and J. Picone, “Low Latency Real-Time Seizure Detection Using Transfer Deep Learning,” in Proceedings of the IEEE Signal Processing in Medicine and Biology Symposium (SPMB), 2021, pp. 1 7. https://www.isip. piconepress.com/publications/conference_proceedings/2021/ieee_spmb/eeg_transfer_learning/. [7] J. Picone, T. Farkas, I. Obeid, and Y. Persidsky, “MRI: High Performance Digital Pathology Using Big Data and Machine Learning,” Philadelphia, Pennsylvania, USA, 2020. https://www.isip.piconepress.com/publications/reports/2020/nsf/mri_dpath/. [8] I. Hunt, S. Husain, J. Simons, I. Obeid, and J. Picone, “Recent Advances in the Temple University Digital Pathology Corpus,” in Proceedings of the IEEE Signal Processing in Medicine and Biology Symposium (SPMB), 2019, pp. 1–4. https://ieeexplore.ieee.org/document/9037859. [9] A. P. Martinez, C. Cohen, K. Z. Hanley, and X. (Bill) Li, “Estrogen Receptor and Cytokeratin 5 Are Reliable Markers to Separate Usual Ductal Hyperplasia From Atypical Ductal Hyperplasia and Low-Grade Ductal Carcinoma In Situ,” Arch. Pathol. Lab. Med., vol. 140, no. 7, pp. 686–689, Apr. 2016. https://doi.org/10.5858/arpa.2015-0238-OA. 
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  5. Obeid, I. ; Selesnick, I. (Ed.)
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