Как построить модель распознавания именованных сущностей (NER) с помощью spaCy для биомедицинского NER на CRAFT corpus?
Мне сложно предварительно обработать xml
файлы, указанные в этом корпусе, в любой формат, используемый spacy
, любая небольшая помощь будет очень признательна. Сначала я преобразовал файлы xml
в формат json
, но это не было принято spacy
. Какой формат обучающих данных ожидает spacy
? Я даже попытался построить свою собственную NER
модель, но не смог предварительно обработать xml
файлы, как указано в этом article.
Вот пример обучения модели NER с использованием spacy, включая ожидаемый формат обучающих данных (из документации spacy):
import random
import spacy
TRAIN_DATA = [
("Uber blew through $1 million a week", {"entities": [(0, 4, "ORG")]}),
("Google rebrands its business apps", {"entities": [(0, 6, "ORG")]})]
nlp = spacy.blank("en")
optimizer = nlp.begin_training()
for i in range(20):
random.shuffle(TRAIN_DATA)
for text, annotations in TRAIN_DATA:
nlp.update([text], [annotations], sgd=optimizer)
nlp.to_disk("/model")
Используемый мной XML-файл доступен в Интернете здесь. Пример записи выглядит так:
<passage>
<infon key="section_type">ABSTRACT</infon>
<infon key="type">abstract</infon>
<offset>141</offset>
<text>
Breast cancer is the most frequent tumor in women, and in nearly two-thirds of cases, the tumors express estrogen receptor alpha (ERalpha, encoded by ESR1). Here, we performed whole-exome sequencing of 16 breast cancer tissues classified according to ESR1 expression and 12 samples of whole blood, and detected 310 somatic mutations in cancer tissues with high levels of ESR1 expression. Of the somatic mutations validated by a different deep sequencer, a novel nonsense somatic mutation, c.2830 C>T; p.Gln944*, in transcriptional regulator switch-independent 3 family member A (SIN3A) was detected in breast cancer of a patient. Part of the mutant protein localized in the cytoplasm in contrast to the nuclear localization of ERalpha, and induced a significant increase in ESR1 mRNA. The SIN3A mutation obviously enhanced MCF7 cell proliferation. In tissue sections from the breast cancer patient with the SIN3A c.2830 C>T mutation, cytoplasmic SIN3A localization was detected within the tumor regions where nuclear enlargement was observed. The reduction in SIN3A mRNA correlates with the recurrence of ER-positive breast cancers on Kaplan-Meier plots. These observations reveal that the SIN3A mutation has lost its transcriptional repression function due to its cytoplasmic localization, and that this repression may contribute to the progression of breast cancer.
</text>
<annotation id="38">
<infon key="identifier">2099</infon>
<infon key="type">Gene</infon>
<infon key="NCBI Homologene">47906</infon>
<location offset="246" length="23"/>
<text>estrogen receptor alpha</text>
</annotation>
<annotation id="39">
<infon key="identifier">2099</infon>
<infon key="type">Gene</infon>
<infon key="NCBI Homologene">47906</infon>
<location offset="271" length="7"/>
<text>ERalpha</text>
</annotation>
<annotation id="40">
<infon key="identifier">2099</infon>
<infon key="type">Gene</infon>
<infon key="NCBI Homologene">47906</infon>
<location offset="291" length="4"/>
<text>ESR1</text>
</annotation>
<annotation id="41">
<infon key="identifier">2099</infon>
<infon key="type">Gene</infon>
<infon key="NCBI Homologene">47906</infon>
<location offset="392" length="4"/>
<text>ESR1</text>
</annotation>
<annotation id="42">
<infon key="identifier">2099</infon>
<infon key="type">Gene</infon>
<infon key="NCBI Homologene">47906</infon>
<location offset="512" length="4"/>
<text>ESR1</text>
</annotation>
<annotation id="43">
<infon key="identifier">25942</infon>
<infon key="type">Gene</infon>
<infon key="NCBI Homologene">32124</infon>
<location offset="720" length="5"/>
<text>SIN3A</text>
</annotation>
<annotation id="44">
<infon key="identifier">2099</infon>
<infon key="type">Gene</infon>
<infon key="NCBI Homologene">47906</infon>
<location offset="868" length="7"/>
<text>ERalpha</text>
</annotation>
<annotation id="45">
<infon key="identifier">2099</infon>
<infon key="type">Gene</infon>
<infon key="NCBI Homologene">47906</infon>
<location offset="915" length="4"/>
<text>ESR1</text>
</annotation>
<annotation id="46">
<infon key="identifier">25942</infon>
<infon key="type">Gene</infon>
<infon key="NCBI Homologene">32124</infon>
<location offset="930" length="5"/>
<text>SIN3A</text>
</annotation>
<annotation id="47">
<infon key="identifier">25942</infon>
<infon key="type">Gene</infon>
<infon key="NCBI Homologene">32124</infon>
<location offset="1048" length="5"/>
<text>SIN3A</text>
</annotation>
<annotation id="48">
<infon key="identifier">25942</infon>
<infon key="type">Gene</infon>
<infon key="NCBI Homologene">32124</infon>
<location offset="1087" length="5"/>
<text>SIN3A</text>
</annotation>
<annotation id="49">
<infon key="identifier">25942</infon>
<infon key="type">Gene</infon>
<infon key="NCBI Homologene">32124</infon>
<location offset="1201" length="5"/>
<text>SIN3A</text>
</annotation>
<annotation id="50">
<infon key="identifier">25942</infon>
<infon key="type">Gene</infon>
<infon key="NCBI Homologene">32124</infon>
<location offset="1331" length="5"/>
<text>SIN3A</text>
</annotation>
<annotation id="51">
<infon key="identifier">9606</infon>
<infon key="type">Species</infon>
<location offset="185" length="5"/>
<text>women</text>
</annotation>
<annotation id="52">
<infon key="identifier">9606</infon>
<infon key="type">Species</infon>
<location offset="762" length="7"/>
<text>patient</text>
</annotation>
<annotation id="53">
<infon key="identifier">9606</infon>
<infon key="type">Species</infon>
<location offset="1031" length="7"/>
<text>patient</text>
</annotation>
<annotation id="54">
<infon key="identifier">29278</infon>
<infon key="type">Species</infon>
<location offset="397" length="10"/>
<text>expression</text>
</annotation>
<annotation id="55">
<infon key="identifier">29278</infon>
<infon key="type">Species</infon>
<location offset="517" length="10"/>
<text>expression</text>
</annotation>
<annotation id="56">
<infon key="identifier">c.2830C>T</infon>
<infon key="type">DNAMutation</infon>
<location offset="1054" length="10"/>
<text>c.2830 C>T</text>
</annotation>
<annotation id="57">
<infon key="identifier">CVCL:0031</infon>
<infon key="type">CellLine</infon>
<location offset="964" length="4"/>
<text>MCF7</text>
</annotation>
<annotation id="58">
<infon key="identifier">MESH:D001943</infon>
<infon key="type">Disease</infon>
<location offset="1494" length="13"/>
<text>breast cancer</text>
</annotation>
<annotation id="59">
<infon key="identifier">MESH:D001943</infon>
<infon key="type">Disease</infon>
<location offset="346" length="13"/>
<text>breast cancer</text>
</annotation>
<annotation id="60">
<infon key="identifier">MESH:D001943</infon>
<infon key="type">Disease</infon>
<location offset="743" length="13"/>
<text>breast cancer</text>
</annotation>
<annotation id="61">
<infon key="identifier">MESH:D001943</infon>
<infon key="type">Disease</infon>
<location offset="1017" length="13"/>
<text>breast cancer</text>
</annotation>
<annotation id="62">
<infon key="identifier">MESH:D009369</infon>
<infon key="type">Disease</infon>
<location offset="477" length="6"/>
<text>cancer</text>
</annotation>
<annotation id="63">
<infon key="identifier">p.Q944*</infon>
<infon key="type">ProteinMutation</infon>
<location offset="642" length="9"/>
<text>p.Gln944*</text>
</annotation>
<annotation id="64">
<infon key="identifier">MESH:D009369</infon>
<infon key="type">Disease</infon>
<location offset="1130" length="5"/>
<text>tumor</text>
</annotation>
<annotation id="65">
<infon key="identifier">MESH:D009369</infon>
<infon key="type">Disease</infon>
<location offset="176" length="5"/>
<text>tumor</text>
</annotation>
<annotation id="66">
<infon key="identifier">c.2830C>T</infon>
<infon key="type">DNAMutation</infon>
<location offset="630" length="10"/>
<text>c.2830 C>T</text>
</annotation>
<annotation id="67">
<infon key="identifier">MESH:D001943</infon>
<infon key="type">Disease</infon>
<location offset="1258" length="14"/>
<text>breast cancers</text>
</annotation>
<annotation id="68">
<infon key="identifier">MESH:D009369</infon>
<infon key="type">Disease</infon>
<location offset="231" length="6"/>
<text>tumors</text>
</annotation>
<annotation id="69">
<infon key="identifier">MESH:D001943</infon>
<infon key="type">Disease</infon>
<location offset="141" length="13"/>
<text>Breast cancer</text>
</annotation>
</passage>
identifier
илиNCBI Homologene
? - person Sam H.   schedule 17.12.2019