11594d79515c4bcdec42959a0881d840a26ab908 jnavarr5 Thu Oct 23 14:08:20 2025 -0700 Need 'useast' in the URL, no Redmine diff --git src/hg/utils/otto/orphanet/parseOrphadata.py src/hg/utils/otto/orphanet/parseOrphadata.py index f9d616a7d75..107ccd0cc66 100755 --- src/hg/utils/otto/orphanet/parseOrphadata.py +++ src/hg/utils/otto/orphanet/parseOrphadata.py @@ -1,728 +1,728 @@ #!/cluster/software/bin/python3.6 import xml.etree.ElementTree as ET import argparse import re import time import sys class Gene(): """ The class Gene() is used for recording the Ensembl gene id, chromosome, start and end chromosomal positions. """ def __init__(self, geneInfo): """ Gene constructor. :param geneInfo: (list) a reformatted line taken directly from hg19.ensGene.gtf (refer to the method getGenesInfo() for more information). Attributes: id: (str) Ensembl geneID, found in position 9 of geneInfo list. chr: (str) Chromosome, found in position 0. start: (str) Chromosomal start position, found in position 3. end: (str) Chromosomal end position, found in position 4. strand: (str) Strand (either + or -) found in position 6. """ self.id = geneInfo[9] self.chr = geneInfo[0] self.start = geneInfo[3] self.end = geneInfo[4] self.strand = geneInfo[6] def printGene(self): """ Prints the attributes of a Gene object. """ print([self.id, self.chr, self.start, self.end, self.strand]) def getEnsGeneInfo(): """ Retrieves all transcript information according to Ensembl gene_id (hg19 and hg38) to be stored in a dictionary, ensemblInfo. Iterates through each transcript line for each gene and creates a Gene object using the transcript with the greatest chromosomal length. The created Gene object stores the gene ID, chromosome, chromosomal positions, and strand. This object is then stored as a value in the ensemblInfo dictionary, with the gene ID as the dictionary key. NOTE: the gene_id ('ENSG...') is used to identify genes because these are the IDs included in the Orphadata files. EnsemblInfo format: { geneID: <Gene object containing gene information> } :return: EnsemblInfo (dict) """ # Downloaded from here: http://hgdownload.soe.ucsc.edu/goldenPath/hg19/bigZips/genes/ # NOTE: we need to download ensembl info hg19ensFile = open("../hg19.ensGene.gtf", "r", encoding='utf-8') hg38ensFile = open("../hg38.ensGene.gtf", "r", encoding='utf-8') # Capture all ensembl transcript information into a dictionary ensemblInfo hg19ensemblInfo = dict() hg38ensemblInfo = dict() # hg19 chromosomal coordinates for line in hg19ensFile: geneInfo = [x.replace('"', "").replace(';', "") for x in line.strip().split()] # reformat, convert to list geneID = geneInfo[9] # grab geneID if geneInfo[2] == 'transcript': if geneID not in hg19ensemblInfo.keys(): # check new gene gene = Gene(geneInfo) hg19ensemblInfo[geneID] = gene # store the Gene object else: # Grab the stored coordinates oldStart = int(hg19ensemblInfo[geneID].start) oldEnd = int(hg19ensemblInfo[geneID].end) # compare the coordinates if abs(int(geneInfo[4]) - int(geneInfo[3])) > abs(oldEnd - oldStart): hg19ensemblInfo[geneID].start = geneInfo[3] hg19ensemblInfo[geneID].end = geneInfo[4] # hg38 chromosomal coorddinates for line in hg38ensFile: geneInfo = [x.replace('"', "").replace(';', "") for x in line.strip().split()] # reformat, convert to list geneID = geneInfo[9] # grab geneID if geneInfo[2] == 'transcript': if geneID not in hg38ensemblInfo.keys(): # check new gene gene = Gene(geneInfo) hg38ensemblInfo[geneID] = gene # store the Gene object else: # Grab the stored coordinates oldStart = int(hg38ensemblInfo[geneID].start) oldEnd = int(hg38ensemblInfo[geneID].end) # compare the coordinates if abs(int(geneInfo[4]) - int(geneInfo[3])) > abs(oldEnd - oldStart): hg38ensemblInfo[geneID].start = geneInfo[3] hg38ensemblInfo[geneID].end = geneInfo[4] # Close the files hg19ensFile.close() hg38ensFile.close() return hg19ensemblInfo, hg38ensemblInfo def parseRareDiseases(disorderDict, ensemblDict): """ Retrieves all disorders and their associated gene information from the Orphadata GENES ASSOCIATED WITH RARE DISEASES file (en_product6.xml). Begins by iterating through the .xml files to find all disorder names, then adds all disorder information to the gene values in ensemblInfo. The data formatted in .xml file is as follows: All disorders are contained within the <DisorderList> tag. Each disorder is separated by the <Disorder id="..."> tag which is not relevant for this script. Instead, the <Name> tag is used to store the disorder information. Within each disorder, there is the <DisorderGeneAssociationList count="X"> tag that includes all genes and gene information associated with the disorder, where X is the total number of associated genes. Each gene is separated by the <DisorderGeneAssociation> tag, which stores all of a specific gene's information within various tags. Of these tags, this script captures the following tag information and stores it in the ensemblInfo dictionary: - <Name> : full name of the gene - <Symbol> : abbreviated symbol of the gene - <Synonym> : abbreviated symbol synonyms - <GeneType> : the type of gene (either gene with protein product, locus, or non-coding RNA) - all <Source> and <Reference> tags that contain 'Ensembl', 'HGNC', 'OMIM' (found within the tag <ExternalReferenceList>) -- NOTE: the Ensembl gene ID contained here is used to grab chromosomal information from the hg19 Ensembl transcript information. If there is no Ensembl gene ID available, then it will not be included in the BED file downstream. - <SourceOfValidation> that contain 'PMID' : includes PMID codes - <Source> : references includng Ensembl, HGNC, OMIM (found in the <ExternalReferenceList> tag) - <DisorderGeneAssociationType> : gene-disease relationship - <DisorderGeneAssociationStatus> : validation status (can be either validated or not validated) - <GeneLocus> : chromosomal location of gene More information regarding the tags can be found in Free access products description file for the GENES ASSOCIATED WITH RARE DISEASES data on Orphadata. :return: updated dictionary containing all disorders and associated genes """ #sys.stdout.write('Finding disorders and associated genes/gene information...') # Open .xml file using ElementTree tree = ET.parse('en_product6.xml') root = tree.getroot() assnValues = dict() assnStatusVals = dict() # Iterate through all disorders for disorder in root[1].findall("Disorder"): diseaseName = disorder.find('Name').text id = disorder.attrib orphaCode = disorder.find('OrphaCode').text if diseaseName not in disorderDict.keys(): disorderDict[diseaseName] = dict() disorderDict[diseaseName].update(id) disorderDict[diseaseName]["orphaCode"] = orphaCode # Link link = disorder.find('ExpertLink').text # Disorder Type disorderType = disorder.find('DisorderType').find('Name').text geneList = disorder.find('DisorderGeneAssociationList') # print(geneInfo.text) # disorderDict[diseaseName].update(geneInfo.attrib) disorderDict[diseaseName]["genes"] = [] # Find Gene Associations: for association in geneList: # One gene per association gene = association.find("Gene") geneDict = dict() geneDict["symbol"] = gene.find("Symbol").text # Source Validation srcValidation = association.find("SourceOfValidation").text geneDict['pmid'] = [] if srcValidation is not None: srcValidation = re.split('_', srcValidation) for src in srcValidation: if 'PMID' in src: id = src.replace('[PMID]', '') geneDict['pmid'].append(id) # Gene Name geneDict["name"] = association.find("Gene").find("Name").text # Gene Synonyms synonyms = [] for syn in gene.find('SynonymList').iter('Synonym'): synonyms.append(syn.text) geneDict['synonyms'] = synonyms # Gene Type geneType = gene.find("GeneType").find("Name").text geneDict['type'] = geneType # References - Ensembl, OMIM, HGNC refList = gene.find('ExternalReferenceList') geneDict['externalRefList'] = [] for ref in refList.iter("ExternalReference"): # iterate through reference list refName = ref.find("Source").text refID = ref.find("Reference").text # Find Ensembl reference if ref.find("Source").text.lower() == "ensembl": ensemblId = ref.find("Reference").text geneDict['ensembl'] = str(ensemblId) # Grab the Ensembl reference link geneDict[ - 'ensemblLink'] = 'https://ensembl.org/Homo_sapiens/Gene/Summary?db=core;g=' + ensemblId + 'ensemblLink'] = 'https://useast.ensembl.org/Homo_sapiens/Gene/Summary?db=core;g=' + ensemblId # Capture ensembl info if ensemblId in ensemblDict.keys(): geneDict['chr'] = ensemblDict[ensemblId].chr geneDict['start'] = ensemblDict[ensemblId].start geneDict['end'] = ensemblDict[ensemblId].end geneDict['strand'] = ensemblDict[ensemblId].strand # Find OMIM reference if refName.lower() == 'omim': geneDict['OMIM'] = str(refID) # Find HGNC reference if refName.lower() == 'hgnc': geneDict['HGNC'] = str(refID) # Gene-Disorder Association Type assnType = association.find("DisorderGeneAssociationType").find('Name').text geneDict['associationType'] = assnType if assnType not in assnValues.keys(): assnValues[assnType] = 1 else: assnValues[assnType] += 1 # Gene-Disorder Association Status assnStatus = association.find("DisorderGeneAssociationStatus").find("Name").text geneDict['assnStatus'] = assnStatus if assnStatus not in assnStatusVals.keys(): assnStatusVals[assnStatus] = 1 else: assnStatusVals[assnStatus] += 1 # Gene Locus locusList = gene.find("LocusList") geneLocus = [] for locus in locusList.iter("GeneLocus"): geneLocus.append(locus.text) geneDict['geneLocus'] = geneLocus # Add gene to disorder disorderDict[diseaseName]["genes"].append(geneDict) # Add attributes to dictionary disorderDict[diseaseName]["expertLink"] = link disorderDict[diseaseName]["type"] = disorderType #sys.stdout.write('Finished finding disorders and genes/gene information.') return disorderDict def parsePhenotypesRareDiseases(disorderDict): """ Stores all phenotypes associated with rare diseases and stores them in the dictionary storing all disorders. Phenotypes are divided into four categories: 'very frequent phenotypes', 'frequent phenotypes', 'occasional phenotypes', and 'rare phenotypes'. HPO IDs and terms are also recorded for each phenotype. The following tags from en_product4.xml are used in this method: - <Name> : the disorder name (found under the <Disorder> tag) - <Source> : PMID sources - <ValidationStatus> : whether the phenotype-disorder relationships are validated - <HPOID> : ID assigned by HPO to a given phenotype - <HPOTerm> : preferred name of HPO phenotype - <HPOFrequency> : estimated frequency of occurrence for a given phenotype in a given clinical entity - <DiagnosticCriteria> : indicates if the given phenotype is a pathognomonic sign or a diagnostic criterion in a given clinical entity Updates these phenotypes for all disorders. :return: updated dictionary containing phenotypes associated with disorders """ #sys.stdout.write('Finding phenotypes associated with Rare Diseases...') # Open .xml files with ElementTree tree = ET.parse('en_product4.xml') root = tree.getroot() # Iterate through all disorder and associated HPO phenotypes for item in root[1].findall("HPODisorderSetStatus"): disorder = item.find("Disorder") diseaseName = disorder.find('Name').text if diseaseName not in disorderDict.keys(): disorderDict[diseaseName] = dict() # Source(s) sources = item.find("Source").text # Validation status & date disorderDict[diseaseName]["valid"] = item.find("ValidationStatus").text disorderDict[diseaseName]["validDate"] = item.find("ValidationDate").text try: disorderDict[diseaseName]["sources"] = sources.split("_") except AttributeError: disorderDict[diseaseName]["sources"] = sources # very frequent phenotypes disorderDict[diseaseName]["very frequent phenotypes"] = [] # frequent phenotype(s) disorderDict[diseaseName]["frequent phenotypes"] = [] # occasional phenotype(s) disorderDict[diseaseName]["occasional phenotypes"] = [] # rare phenotype(s) disorderDict[diseaseName]["rare phenotypes"] = [] for association in disorder.find("HPODisorderAssociationList"): # HPO id hpoId = association.find("HPO").find("HPOId").text # HPO Name hpoName = association.find("HPO").find("HPOTerm").text # HPO Frequency hpoFrequency = association.find("HPOFrequency").find("Name").text # Diagnostic Criteria try: hpoDiagnostic = association.find("DiagnosticCriteria").text.strip() except AttributeError: hpoDiagnostic = association.find("DiagnosticCriteria").text # Tuple format to create <a> tags in details page x = (hpoName, hpoId) # categorize frequencies if hpoFrequency == 'very frequent (99-80%)': disorderDict[diseaseName]["very frequent phenotypes"].append(x) elif hpoFrequency == 'Frequent (79-30%)': disorderDict[diseaseName]["frequent phenotypes"].append(x) elif hpoFrequency == 'Occasional (29-5%)': disorderDict[diseaseName]["occasional phenotypes"].append(x) elif 'Very rare ' in hpoFrequency: disorderDict[diseaseName]["rare phenotypes"].append(x) return disorderDict def parseRareDiseaseEpi(disorderDict): """ Stores all prevalance(s) for disorders and updates the disorderDict using the epidemiological data from Orphadata. The following .xml tags from en_product9_prev.xml are used in this method: - <Name> (within <Disorder> tag): disorder name - <PrevalenceType> : the name of the prevalence type (can be "Point prevalence", "birth prevalence", "lifelong prevalence", "incidence", "cases/families") - <PrevalenceQualification> : prevalence qualification name (can be either "Value and Class", "Only class", "Case" or "Family") - <Source> : source(s) of information of a given prevalence type for disorder - <PrevalenceClass> : estimated prevalence of disorder - <ValMoy> : mean value of a given prevalence type - <PrevalenceGeographic> : geographic area of a given prevalence type - <PrevalenceValidationStatus> : can be either: "Validated" or "Not yet validated" More information regarding these tags and other tags used in this file can be found via the Orphadata Free Access Products file. """ # Open .xml files with ElementTree tree = ET.parse('en_product9_prev.xml') root = tree.getroot() # Iterate through disorders for item in root.find("DisorderList"): name = item.find("Name").text if name not in disorderDict.keys(): # add disorder if not already recorded disorderDict[name] = dict() # Grab prevalence(s) prevalences = dict() for prev in item.find("PrevalenceList"): try: prevType = prev.find("PrevalenceType").find("Name").text prevalences[prevType] = dict() except AttributeError: break try: prevQual = prev.find("PrevalenceQualification").find("Name").text prevalences[prevType]["qualification"] = prevQual except AttributeError: pass try: prevSrc = prev.find("Source").text.split('_') prevalences[prevType]["source(s)"] = prevSrc except AttributeError: pass try: prevClass = prev.find("PrevalenceClass").find("Name").text prevalences[prevType]["class"] = prevClass except AttributeError: pass try: valMoy = prev.find("ValMoy").text prevalences[prevType]["valmoy"] = valMoy except AttributeError: pass try: prevGeo = prev.find("PrevalenceGeographic").find("Name").text prevalences[prevType]["geographic"] = prevGeo except AttributeError: pass try: prevValidStatus = prev.find("PrevalenceValidationStatus").find("Name").text prevalences[prevType]["validation"] = prevValidStatus except AttributeError: pass # Add the prevalence info to the disorder disorderDict[name]["prevalence(s)"] = prevalences #sys.stdout.write('Finished finding epidemiological data.') def naturalHistory(disorderDict): """ Parses through disorders listed in en_product1.xml to retrieve disorder attributes relating to natural history. The disorder dictionary is then updated with this information. The following .xml tags from en_product9_ages.xml is used in this method: - <Name> (found within <Disorder> tag) : name of the disorder - <AverageAgeOfOnset> : class based on estimated average age of disorder onset; found within the <AverageAgeOfOnsetList> tag - <AverageAgeOfDeath> : classes based on the estimated average age at death for a given disorder; found within the <AverageAgeOfDeathList> tag - <TypeOfInheritance> : type(s) of inheritance associated with a given disorder; found within the <TypeOfInheritanceList> tag More information regarding these tags and other tags used in this file can be found via the Orphadata Free Access Products file. """ #sys.stdout.write('Finding ages of onset, death, and inheritance types...') # Open .xml file using ElementTree tree = ET.parse('en_product9_ages.xml') root = tree.getroot() inheritanceValues = dict() onsetValues = dict() # Iterate through disorders for item in root.find("DisorderList"): name = item.find("Name").text # Add disorders if not yet recorded if name not in disorderDict.keys(): disorderDict[name] = dict() # Average Age of Onset List disorderDict[name]["onsetList"] = [] for onset in item.find("AverageAgeOfOnsetList"): onsetType = onset.find("Name").text disorderDict[name]["onsetList"].append(onsetType) if onsetType not in onsetValues.keys(): onsetValues[onsetType] = 1 else: onsetValues[onsetType] += 1 # Average Age of Death List disorderDict[name]["deathList"] = [] # removed the following as AverageAgeOfDeath is not in XML anymore, Max, Dec 12 2022 #for ageDeath in item.find("AverageAgeOfDeathList"): # disorderDict[name]["deathList"].append(ageDeath.find("Name").text) # Inheritance List disorderDict[name]["inheritance"] = [] for inheritType in item.find("TypeOfInheritanceList"): inheritance = inheritType.find("Name").text disorderDict[name]["inheritance"].append(inheritance) if inheritance not in inheritanceValues.keys(): inheritanceValues[inheritance] = 1 else: inheritanceValues[inheritance] += 1 #sys.stdout.write('Finished finding onset/death/inheritance information.') return disorderDict def createBed(disorderDict, assembly): """ Creates the final BED file using all disorders/genes and other information. This method begins by iterating through each disorder in disorderDict. For each gene associated with a given disorder, the method creates one entry in the BED file that includes the disorder name, chromosomal positions, and other aggregated information from the previous methods. For example, given a disorder "Disorder1" with three genes associated with the disorder, "GeneA", "GeneB", and "GeneC", resulting BED file will appear as follows: <GeneA chr> <GeneA start> <GeneA end> <Disorder1 ID> ... <Disorder1 Name> ... <disorder info> <GeneB chr> <GeneB start> <GeneB end> <Disorder1 ID> ... <Disorder1 Name> ... <disorder info> <GeneC chr> <GeneC start> <GeneC end> <Disorder1 ID> ... <Disorder1 Name> ... <disorder info> NOTE: disorders with no genes associated are skipped and not included in the BED file. The BED file fields for the Orphadata information are included below: 1. chrom : name of chromosome in which gene exists (required) 2. chromStart : start position of gene (required) 3. chromEnd : end position of gene (required) 4. name : name of the BED line; the OrphaCode for each disorder is used here 5. score : score between 0 and 1000; not relevant to this track and is by default 0 6. strand : defines the strand, either "+", "-", or "." for no strand 7. thickStart : start position where gene is drawn thickly (same as field 2) 8. thickEnd : end position where gene is drawn thickly (same as field 3) 9. itemRgb : color of the item 10. disorderName : name of the disorder 11. geneSymbol : HGNC-approved gene symbol 12. geneName : gene name 13. ensemblID : identifier used within Ensembl database 14. geneType : the type of gene 15. geneLocus : gene chromosomal location 16. assnStatus : whether disorder-gene association is validated or not 17. assnType : type of gene-disease relationship 18. pmid : PMID reference(s) 19. orphaCode : unique numerical identifier internal to Orphanet 20. omim : OMIM reference 21. hgnc : HGNC reference 22. inheritance : type(s) of inheritance associated with the disorder 23. onsetList : list of ages of onset associated with the disorder 24. deathList : list of average ages of death associated with the disorder 25. prevalences : types of prevalence associated with disorder 26. verFreqPhen : very frequent phenotype(s) 27. freqPhen : frequent phenotype(s) 28. occasPhen : occasional phenotype(s) 29. rarePhen : rare phenotype(s) """ # Create new BED file # NOTE: encoding for utf-8 is required since several disorders contain special characters that are not included in # ascii encoding. f = open('orphadata.'+assembly+'.bed', "w", encoding='utf-8') # Iterate through disorders for disease in disorderDict.keys(): # Only include disorders with genes associated if 'genes' in disorderDict[disease]: # Iterate through genes for gene in disorderDict[disease]['genes']: row = [] # stores the info for each BED line # Only include if chromosome is included in gene information if 'chr' in gene.keys(): # Fields: 1 chr, 2 start, 3 end row.append(str(gene['chr'])) row.append(str(gene['start'])) row.append(str(gene['end'])) # Field 4: name of BED line row.append(disorderDict[disease]['orphaCode']) # Field 5: no score, place 0 row.append('0') # Field 6: strand if 'strand' in gene.keys(): row.append(str(gene["strand"])) else: # if no strand is included row.append('.') # Fields 7, 8: Thick start and end (same as fields 2 and 3) row.append(str(gene['start'])) row.append(str(gene['end'])) # Field 9: itemRgb row.append('0,146,156') # Field 10: Disorder name row.append(disease) # Field 11: geneSymbol (visible in description, mouseover) row.append(str(gene['symbol'])) # Field 12: geneName (visible in description) row.append(str(gene['name'])) # Field 13: ensemblID row.append(gene['ensembl']) # Field 14: geneType (visible in description) row.append(str(gene['type'])) # Field 15: geneLocus (visible in description) row.append(' '.join(x for x in gene['geneLocus'])) # Field 16: association status row.append(str(gene['assnStatus'])) # Field 17: association type row.append(str(gene['associationType'])) # Field 18: PMID(s) row.append(str(','.join(x for x in gene['pmid']))) # Field 19: Orphacode row.append(disorderDict[disease]['orphaCode']) # Field 20: OMIM ID if 'OMIM' in gene.keys(): row.append(gene['OMIM']) else: row.append('') # Field 21: HGNC ID if 'HGNC' in gene.keys(): row.append(gene['HGNC']) else: row.append('') # Field 22: Inheritance (visible in description, mouseover) if 'inheritance' not in disorderDict[disease].keys(): row.append('') else: row.append(', '.join(x for x in disorderDict[disease]['inheritance'])) # Field 23: Onset List if 'onsetList' not in disorderDict[disease].keys(): row.append('') else: row.append(', '.join(x for x in disorderDict[disease]['onsetList'])) # Field 24: Death List if 'deathList' not in disorderDict[disease].keys(): row.append('') else: row.append(', '.join(x for x in disorderDict[disease]['deathList'])) # Field 25: prevalence(s) if 'prevalence(s)' not in disorderDict[disease].keys(): row.append('') else: row.append(', '.join(str(x) for x in disorderDict[disease]['prevalence(s)'])) # NOTE: The following fields featuring phenotype(s) are formatted according to the extraTabelFields format (refer to bigBed documentation). # Field 26: very frequent phenotype(s) if 'very frequent phenotypes' in disorderDict[disease].keys() and len( disorderDict[disease]['very frequent phenotypes']) > 0: row.append(', '.join('<a href="https://hpo.jax.org/app/browse/term/'+x[1]+'" target="_blank">'+x[0]+'</a>' for x in disorderDict[disease]['very frequent phenotypes'])) else: row.append('') # Field 27: frequent phenotype(s) if 'frequent phenotypes' in disorderDict[disease].keys() and len( disorderDict[disease]['frequent phenotypes']) > 0: row.append(', '.join('<a href="https://hpo.jax.org/app/browse/term/'+x[1]+'" target="_blank">'+x[0]+'</a>' for x in disorderDict[disease]['frequent phenotypes'])) else: row.append('') # Field 28: occasional phenotype(s) if 'occasional phenotypes' in disorderDict[disease].keys() and len( disorderDict[disease]['occasional phenotypes']) > 0: row.append(', '.join('<a href="https://hpo.jax.org/app/browse/term/'+x[1]+'" target="_blank">'+x[0]+'</a>' for x in disorderDict[disease]['occasional phenotypes'])) else: row.append('') # Field 29: rare phenotype(s) if 'rare phenotypes' in disorderDict[disease].keys() and len( disorderDict[disease]['rare phenotypes']) > 0: row.append(', '.join('<a href="https://hpo.jax.org/app/browse/term/'+x[1]+'" target="_blank">'+x[0]+'</a>' for x in disorderDict[disease]['rare phenotypes'])) else: row.append('') # Write line to BED file f.write('\t'.join(x for x in row)) # add new line f.write('\n') f.close() def main(): """ Calls all methods required for downloading Orphadata files and creating BED file. """ # Grab timestamp parser = argparse.ArgumentParser(description='Downloads most recent Orphadata files and generates a BED file for Orphadata track hub.') #parser.add_argument("-t", "--timestamp", help="The timestamp at which script is called.", required=True) args = parser.parse_args() #timestamp = args.timestamp startTime = time.time() # Create Ensembl dictionaries for hg19 and hg38 hg19ensemblDict, hg38ensemblDict = getEnsGeneInfo() # Create dictonary to store disorders hg19disorderDict = dict() hg38disorderDict = dict() # 1. Parse Rare Diseases parseRareDiseases(hg19disorderDict, hg19ensemblDict) parseRareDiseases(hg38disorderDict, hg38ensemblDict) # 2. Parse Phenotypes of Rare Diseases parsePhenotypesRareDiseases(hg19disorderDict) parsePhenotypesRareDiseases(hg38disorderDict) # 3. Parse Epidemology Prevalences parseRareDiseaseEpi(hg19disorderDict) parseRareDiseaseEpi(hg38disorderDict) # 4. Natural History (ages) naturalHistory(hg19disorderDict) naturalHistory(hg38disorderDict) # 5. Create BED files createBed(hg19disorderDict, assembly='hg19') createBed(hg38disorderDict, assembly='hg38') #print("Time elapsed: ", time.time() - startTime) if __name__ == "__main__": main()