Description
Named Entity recognition annotator allows for a generic model to be trained by utilizing a deep learning algorithm (Char CNNs - BiLSTM - CRF - word embeddings) inspired on a former state of the art model for NER: Chiu & Nicols, Named Entity Recognition with Bidirectional LSTM,CNN.Pretrained named entity recognition deep learning model for biology and genetics terms.
Predicted Entities
DNA, RNA, cell_line, cell_type, protein.
Live Demo Open in Colab Copy S3 URI
How to use
document_assembler = DocumentAssembler()\
.setInputCol("text")\
.setOutputCol("document")
sentence_detector = SentenceDetector()\
.setInputCols(["document"])\
.setOutputCol("sentence")
tokenizer = Tokenizer()\
.setInputCols(["sentence"])\
.setOutputCol("token")
word_embeddings = WordEmbeddingsModel.pretrained("embeddings_clinical", "en", "clinical/models")\
.setInputCols(["sentence", "token"])\
.setOutputCol("embeddings")
clinical_ner = MedicalNerModel.pretrained("ner_cancer_genetics", "en", "clinical/models") \
.setInputCols(["sentence", "token", "embeddings"]) \
.setOutputCol("ner")
ner_converter = NerConverter()\
.setInputCols(["sentence", "token", "ner"])\
.setOutputCol("ner_chunk")
nlp_pipeline = Pipeline(stages=[document_assembler, sentence_detector, tokenizer, word_embeddings, clinical_ner, ner_converter])
model = nlp_pipeline.fit(spark.createDataFrame([[""]]).toDF("text"))
results = model.transform(spark.createDataFrame([['The human KCNJ9 (Kir 3.3, GIRK3) is a member of the G-protein-activated inwardly rectifying potassium (GIRK) channel family. Here we describe the genomicorganization of the KCNJ9 locus on chromosome 1q21-23 as a candidate gene forType II diabetes mellitus in the Pima Indian population. The gene spansapproximately 7.6 kb and contains one noncoding and two coding exons separated byapproximately 2.2 and approximately 2.6 kb introns, respectively. We identified14 single nucleotide polymorphisms (SNPs), including one that predicts aVal366Ala substitution, and an 8 base-pair (bp) insertion/deletion. Ourexpression studies revealed the presence of the transcript in various humantissues including pancreas, and two major insulin-responsive tissues: fat andskeletal muscle. The characterization of the KCNJ9 gene should facilitate furtherstudies on the function of the KCNJ9 protein and allow evaluation of thepotential role of the locus in Type II diabetes.']], ["text"]))
val document_assembler = new DocumentAssembler()
.setInputCol("text")
.setOutputCol("document")
val sentence_detector = new SentenceDetector()
.setInputCols("document")
.setOutputCol("sentence")
val tokenizer = new Tokenizer()
.setInputCols("sentence")
.setOutputCol("token")
val word_embeddings = WordEmbeddingsModel.pretrained("embeddings_clinical", "en", "clinical/models")
.setInputCols(Array("sentence", "token"))
.setOutputCol("embeddings")
val ner = MedicalNerModel.pretrained("ner_cancer_genetics", "en", "clinical/models")
.setInputCols(Array("sentence", "token", "embeddings"))
.setOutputCol("ner")
val ner_converter = new NerConverter()
.setInputCols(Array("sentence", "token", "ner"))
.setOutputCol("ner_chunk")
val pipeline = new Pipeline().setStages(Array(document_assembler, sentence_detector, tokenizer, word_embeddings, ner, ner_converter))
val data = Seq("""The human KCNJ9 (Kir 3.3, GIRK3) is a member of the G-protein-activated inwardly rectifying potassium (GIRK) channel family. Here we describe the genomicorganization of the KCNJ9 locus on chromosome 1q21-23 as a candidate gene forType II diabetes mellitus in the Pima Indian population. The gene spansapproximately 7.6 kb and contains one noncoding and two coding exons separated byapproximately 2.2 and approximately 2.6 kb introns, respectively. We identified14 single nucleotide polymorphisms (SNPs), including one that predicts aVal366Ala substitution, and an 8 base-pair (bp) insertion/deletion. Ourexpression studies revealed the presence of the transcript in various humantissues including pancreas, and two major insulin-responsive tissues: fat andskeletal muscle. The characterization of the KCNJ9 gene should facilitate furtherstudies on the function of the KCNJ9 protein and allow evaluation of thepotential role of the locus in Type II diabetes.""").toDS().toDF("text")
val result = pipeline.fit(data).transform(data)
import nlu
nlu.load("en.med_ner.cancer").predict("""The human KCNJ9 (Kir 3.3, GIRK3) is a member of the G-protein-activated inwardly rectifying potassium (GIRK) channel family. Here we describe the genomicorganization of the KCNJ9 locus on chromosome 1q21-23 as a candidate gene forType II diabetes mellitus in the Pima Indian population. The gene spansapproximately 7.6 kb and contains one noncoding and two coding exons separated byapproximately 2.2 and approximately 2.6 kb introns, respectively. We identified14 single nucleotide polymorphisms (SNPs), including one that predicts aVal366Ala substitution, and an 8 base-pair (bp) insertion/deletion. Ourexpression studies revealed the presence of the transcript in various humantissues including pancreas, and two major insulin-responsive tissues: fat andskeletal muscle. The characterization of the KCNJ9 gene should facilitate furtherstudies on the function of the KCNJ9 protein and allow evaluation of thepotential role of the locus in Type II diabetes.""")
Results
+-------------------+---------+
| token|ner_label|
+-------------------+---------+
| The| O|
| human|B-protein|
| KCNJ9|I-protein|
| (| O|
| Kir|B-protein|
| 3.3|I-protein|
| ,| O|
| GIRK3|B-protein|
| )| O|
| is| O|
| a| O|
| member| O|
| of| O|
| the| O|
|G-protein-activated|B-protein|
| inwardly|I-protein|
| rectifying|I-protein|
| potassium|I-protein|
| (|I-protein|
| GIRK|I-protein|
| )|I-protein|
| channel|I-protein|
| family|I-protein|
| .| O|
| Here| O|
| we| O|
| describe| O|
| the| O|
|genomicorganization| O|
| of| O|
| the| O|
| KCNJ9| B-DNA|
| locus| I-DNA|
| on| O|
| chromosome| B-DNA|
| 1q21-23| I-DNA|
+-------------------+---------+
Model Information
| Model Name: | ner_cancer_genetics |
| Compatibility: | Healthcare NLP 3.0.0+ |
| License: | Licensed |
| Edition: | Official |
| Input Labels: | [sentence, token, embeddings] |
| Output Labels: | [ner] |
| Language: | en |
Data Source
Trained on Cancer Genetics (CG) task of the BioNLP Shared Task 2013 with embeddings_clinical.
https://aclanthology.org/W13-2008/
Benchmarking
label tp fp fn prec rec f1
B-cell_line 581 148 151 0.79698217 0.79371583 0.79534566
I-DNA 2751 735 317 0.7891566 0.89667535 0.8394873
I-protein 4416 867 565 0.8358887 0.88656896 0.8604832
B-protein 5288 763 660 0.8739051 0.8890383 0.8814068
I-cell_line 1148 244 301 0.82471263 0.79227054 0.80816615
I-RNA 221 60 27 0.78647685 0.891129 0.83553874
B-RNA 157 40 36 0.79695433 0.8134715 0.8051282
B-cell_type 1127 292 250 0.7942213 0.8184459 0.8061516
I-cell_type 1547 392 263 0.7978339 0.85469615 0.82528675
B-DNA 1513 444 387 0.77312213 0.7963158 0.7845475
Macro-average prec: 0.8069253, rec: 0.84323275, f1: 0.82467955
Micro-average prec: 0.82471186, rec: 0.86377037, f1: 0.84378934