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logger.debug("For "+str(spliced_species_num)+" species, out of "+str(len(isoform_by_gene_all))+" , we have splice files.")
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iftotal_genes==0:
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logger.debug("It seems that in all of the splice files, each line has only one item. Make sure that the splitter in each line is semicolon ; ")
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logger.debug("No splice information found. It could be that each line of splice fileshas only one item. Make sure that the splitter in each line is semicolon ; . Or the splice folder is empty. You need to delete the empty splice folder. FastOMA check input failed! Exiting...")
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sys.exit(1)
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logger.debug("In total, for "+str(total_genes)+" genes, we have "+str(total_isoforms)+" splices.")
logger.error("Halting FastOMA because of invalid proteome input data")
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logger.error("Halting FastOMA because of invalid proteome input data. FastOMA check input failed! Exiting...")
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sys.exit(1)
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try:
@@ -239,7 +239,7 @@ def fastoma_check_input():
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species_tree=Tree(conf.species_tree)
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# todo add check fro Phyloxml
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except:
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logger.error("We have problem with parsing species tree %s using ete3 Tree. Maybe there are some special chars.", conf.species_tree)
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logger.error("We have problem with parsing species tree %s using ete3 Tree. Maybe there are some special chars. FastOMA check input failed! Exiting...", conf.species_tree)
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