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| WITH dx_case_inclusion_criteria_1 AS ( | |
| SELECT co.person_id, cohort.standard_code_set AS code_set | |
| FROM | |
| {database}.condition_occurrence co, | |
| {database}.HYPOTHYROIDISM_COHORT_VARS cohort | |
| WHERE | |
| co.condition_concept_id = CAST(cohort.standard_concept_id AS int64) | |
| AND cohort.phenotype_definition_number = 0 | |
| AND cohort.standard_code_set = {code_set_group} | |
| GROUP BY co.person_id, cohort.standard_code_set |
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| WITH rx_case_inclusion_criteria_1 AS ( | |
| SELECT de.person_id, cohort.standard_code_set AS code_set | |
| FROM | |
| {database}.drug_exposure de, | |
| {database}.STEROIDINDUCEDOSTEONECROSIS_COHORT_VARS cohort | |
| WHERE de.route_concept_id IN (4132161, 4171047, 4302612) | |
| AND de.drug_concept_id = CAST(cohort.standard_concept_id AS int64) | |
| AND cohort.phenotype_definition_number = 1 | |
| AND cohort.standard_code_set = {code_set_group} | |
| GROUP BY |
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| -- get unique counts of source and standard codes for each phenotype | |
| -- CHCO | |
| SELECT standard_code_set, COUNT(DISTINCT source_code) AS source_code_count, COUNT(DISTINCT standard_code) AS standard_code_count | |
| FROM CHCO_DeID_Oct2018.ADHD_COHORT_VARS | |
| WHERE standard_code_set is NOT NULL | |
| GROUP BY standard_code_set | |
| SELECT standard_code_set, COUNT(DISTINCT source_code) AS source_code_count, COUNT(DISTINCT standard_code) AS standard_code_count | |
| FROM CHCO_DeID_Oct2018.APPENDICITIS_COHORT_VARS |
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| SELECT * FROM | |
| (SELECT patient_id, disease_group_label, disease_group_num, disease_group_abbreviation, condition_concept_id AS concept_id, visit_occurrence_id, visit_start_interval | |
| FROM CHCO_DeID_Oct2018.Med2Mech_RareDisease_Conditions | |
| WHERE visit_start_interval>0 AND visit_end_interval>0) | |
| UNION ALL | |
| (SELECT patient_id, disease_group_label, disease_group_num, disease_group_abbreviation, drug_concept_id AS concept_id, visit_occurrence_id, visit_start_interval | |
| FROM CHCO_DeID_Oct2018.Med2Mech_RareDisease_Medications | |
| WHERE visit_start_interval>0 AND visit_end_interval>0) |
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| -- Query 1: Search for specific patients using specific vocabulary codes | |
| SELECT DISTINCT | |
| CONCAT('"', CAST(c1.concept_id AS STRING), '"') AS OMOP_ID, | |
| c1.concept_name AS OMOP_LABEL, | |
| CONCAT('"', CAST(c.concept_code AS STRING), '"') AS CLINICAL_CODE, | |
| CONCAT('"', CAST(c1.concept_code AS STRING), '"') AS SNOMED_CODE, | |
| c.vocabulary_id AS VOCABULARY | |
| FROM CHCO_DeID_Oct2018.concept c | |
| JOIN CHCO_DeID_Oct2018.concept_relationship r ON r.concept_id_1 = c.concept_id |
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| ############ | |
| ## PURPOSE: Generate gene-centric edge lists for collaboration with PNNL | |
| ## Master Repo: https://github.com/callahantiff/PheKnowLator/wiki/v2.0.0 | |
| ## Edge Data: https://github.com/callahantiff/PheKnowLator/wiki/v2-Data-Sources | |
| ########### | |
| # import needed libraries | |
| import pandas | |
| import pickle | |
| import json |
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| #!/usr/bin/env python | |
| # -*- coding: utf-8 -*- | |
| # import needed libraries | |
| import glob | |
| import json | |
| import os | |
| import pickle | |
| import random | |
| import requests |
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| #!/usr/bin/env python3.6.2 | |
| # -*- coding: utf-8 -*- | |
| # run script from command line via python3 keyword_search_github_repositories.py | |
| import click | |
| import datetime | |
| import time | |
| from github import Github |
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| # PURPOSE: This query is designed to query an OMOP instance and return 6 columns. | |
| # This query makes the assumption that the other shops would be willing to return | |
| # some results to us, rather than calculating coverage statistics locally | |
| WITH | |
| condition_concepts | |
| AS (SELECT | |
| c.condition_concept_id AS CONCEPT_ID, | |
| c1.concept_name AS CONCEPT_LABEL, | |
| v.vocabulary_version AS VOCABULARY_VERSION, |