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README.md
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- [Contributions](#contributions)
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## Dataset Description
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- **Homepage:** [Github](https://github.com/ZihanWangKi/CrossWeigh)
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- **Repository:** [Github](https://github.com/ZihanWangKi/CrossWeigh)
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- **Paper:** Pending
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### Dataset Summary
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EpiSet4NER is a dataset
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[NIH NCATS GARD](https://rarediseases.info.nih.gov/)
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An example of 'train' looks as follows.
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"ner_tags": [0, 0, 0, 3, 0, 0, 0, 0, 0, 1, 0, 5, 6, 0],
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}
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```
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### Data Fields
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The data fields are the same among all splits.
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#### conllpp
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- `id`: a `string` feature.
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- `tokens`: a `list` of `string` features.
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- `ner_tags`: a `list` of classification labels, with possible values including `O` (0), `B-
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"O", #(0)
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"B-LOC", #(1)
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"I-LOC", #(2)
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"B-EPI", #(3)
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"I-EPI", #(4)
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"B-STAT", #(5)
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"I-STAT", #(6)
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### Data Splits
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|EpiSet |
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## Dataset Creation
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### Curation Rationale
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[More Information Needed]
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### Discussion of Biases
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### Other Known Limitations
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- [Contributions](#contributions)
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## Dataset Description
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- **Repository:** [Github](https://github.com/ncats/epi4GARD/tree/master/EpiExtract4GARD#epiextract4gard)
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- **Paper:** Pending
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### Dataset Summary
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EpiSet4NER is a bronze-standard dataset for epidemiological entity recognition of location, epidemiologic types, and created using weakly-supervised teaching methods
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locations, epidemiological identifiers (e.g. "prevalence", "annual incidence", "estimated occurrence") and epidemiological rates (e.g. "1.7 per 1,000,000 live births", "2.1:1.000.000", "one in five million", "0.03%")
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These are the V3 training (456 abstracts), validation (114 abstracts), and programmatically generated test (50 abstracts) set. The training set was copied to ```datasets/EpiCustomV3``` and renamed *train.tsv*. The validation set was copied to ```datasets/EpiCustomV3``` and ```datasets/Large_DatasetV3``` and renamed *val.tsv*. The V3 test set (uncorrected) is important as it is used by *Find efficacy of test predictions.ipynb* to find the efficacy of the programmatic labeling, but was otherwise not used with the model.
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[NIH NCATS GARD](https://rarediseases.info.nih.gov/)
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An example of 'train' looks as follows.
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"ner_tags": [0, 0, 0, 3, 0, 0, 0, 0, 0, 1, 0, 5, 6, 0],
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}
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```
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### Data Fields
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The data fields are the same among all splits.
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- `id`: a `string` feature.
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- `tokens`: a `list` of `string` features.
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- `ner_tags`: a `list` of classification labels, with possible values including `O` (0), `B-LOC` (1), `I-LOC` (2), `B-EPI` (3), `I-EPI` (4),`B-STAT` (5),`I-STAT` (6).
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### Data Splits by number of tokens
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|name |train |validation|test|
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|---------|-----:|----:|----:|
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|EpiSet |117888|31262|13910|
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## Dataset Creation
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This bronze-standard dataset was created from 620 rare disease abstracts
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Programmatic Labeling using statistical and rule-based methods (Weakly Supervised Teaching)
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![Text Labeling](https://raw.githubusercontent.com/ncats/epi4GARD/master/EpiExtract4GARD/datasets/EpiCustomV3/Text%20Labeling4.png)
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### Curation Rationale
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[More Information Needed]
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### Discussion of Biases
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Generates *whole_abstract_set.csv* and *positive_abstract_set.csv*. *whole_abstract_set.csv* is a dataset created by sampling 500 rare disease names and their synonyms from *GARD.csv* until ≥50 abstracts had been returned or the search results were exhausted. Although ~25,000 abstracts were expected, 7699 unique abstracts were returned due to the limited research on rare diseases. After running each of these through the LSTM RNN classifier, the *positive_abstract_set.csv* was created from the abstracts which had an epidemiological probability >50%. *positive_abstract_set.csv* will be passed to *create_labeled_dataset_V2.ipynb*
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### Other Known Limitations
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