コード例 #1
0
def normexp_matrix_IDs(global_variables, out_path, biotype):

    out_file = open(os.path.join(out_path, "data", "normexp_matrix_IDs.csv"),
                    "w")

    master_gene_table = global_variables["master_gene_table"]

    # gets the header
    header_list = ["ID"]
    header_list += get_gene_normexp_header(global_variables)
    out_file.write("\t".join(header_list) + "\n")

    # gets the gene expression
    for gene_ID in master_gene_table:
        gene_dictionary = master_gene_table[gene_ID]

        # tests for a valid gene:
        valid_gene = False
        if gene_dictionary["normexp_flag"]:
            if global_variables["GENE_BIOTYPE_FLAG"] and (
                    gene_dictionary["BIOTYPE"] == biotype
                    or biotype == "all_genes"):
                valid_gene = True
            if global_variables["GENE_BIOTYPE_FLAG"] == False:
                valid_gene = True

        if valid_gene:
            gene_out_list = [gene_ID]
            gene_out_list += get_gene_normexp(global_variables,
                                              gene_dictionary)
            out_file.write("\t".join(str(x) for x in gene_out_list) + "\n")
コード例 #2
0
def MPDE_any_significant_annotated(global_variables, out_path, biotype,
                                   pde_IDs):

    out_file = open(
        os.path.join(out_path, "data",
                     "genes_significant_in_any_PDEs_annotated.csv"), "w")

    master_gene_table = global_variables["master_gene_table"]

    # gets the header
    header_list = ["ID"]
    header_list += get_gene_background_header(global_variables)
    header_list += get_gene_mpde_header(pde_IDs)
    header_list += get_gene_normexp_header(global_variables)
    header_list += get_gene_normexp_stats_header(global_variables)
    header_list += get_gene_annotations_header(global_variables)
    out_file.write("\t".join(header_list) + "\n")

    # gets the genes
    for gene_ID in master_gene_table:
        gene_dictionary = master_gene_table[gene_ID]

        # tests for a valid gene:
        valid_gene = False
        present_in_any_pde = False

        if gene_dictionary["normexp_flag"]:

            if (global_variables["GENE_BIOTYPE_FLAG"] and
                (gene_dictionary["BIOTYPE"] == biotype
                 or biotype == "all_genes")
                ) or global_variables["GENE_BIOTYPE_FLAG"] == False:
                valid_gene = True

                for pde_ID in pde_IDs:
                    if pde_ID not in gene_dictionary:
                        valid_gene = False
                    else:
                        pde_Dict = gene_dictionary[pde_ID]
                        if not pde_Dict["in_gl"]:
                            valid_gene = False
                        if pde_Dict["sig"]:
                            present_in_any_pde = True

        if valid_gene and present_in_any_pde:
            gene_out_list = [gene_ID]
            gene_out_list += get_gene_background(global_variables,
                                                 gene_dictionary)
            gene_out_list += get_gene_mpde(global_variables, gene_dictionary,
                                           pde_IDs)
            gene_out_list += get_gene_normexp(global_variables,
                                              gene_dictionary)
            gene_out_list += get_gene_normexp_stats(global_variables,
                                                    gene_dictionary)
            gene_out_list += get_gene_annotations(global_variables,
                                                  gene_dictionary)
            out_file.write("\t".join(str(x) for x in gene_out_list) + "\n")
コード例 #3
0
def PDE_annotated_significant_upregulated(global_variables, out_path, biotype,
                                          pde_ID):

    out_file = open(
        os.path.join(out_path, "data",
                     "PDE_annotated_significant_upregulated.csv"), "w")

    master_gene_table = global_variables["master_gene_table"]

    # gets the header
    header_list = ["ID"]
    header_list += get_gene_background_header(global_variables)
    header_list += get_gene_pde_header(global_variables)
    header_list += get_gene_normexp_header(global_variables)
    header_list += get_gene_normexp_stats_header(global_variables)
    header_list += get_gene_annotations_header(global_variables)
    out_file.write("\t".join(header_list) + "\n")

    # gets the genes
    for gene_ID in master_gene_table:
        gene_dictionary = master_gene_table[gene_ID]

        # tests for a valid gene:
        valid_gene = False
        if gene_dictionary["normexp_flag"] and pde_ID in gene_dictionary:
            pde_Dict = gene_dictionary[pde_ID]
            if pde_Dict["in_gl"] and pde_Dict[
                    "sig"] and pde_Dict["log2fold"] > 0:
                if global_variables["GENE_BIOTYPE_FLAG"] and (
                        gene_dictionary["BIOTYPE"] == biotype
                        or biotype == "all_genes"):
                    valid_gene = True
                if global_variables["GENE_BIOTYPE_FLAG"] == False:
                    valid_gene = True

        if valid_gene:
            gene_out_list = [gene_ID]
            gene_out_list += get_gene_background(global_variables,
                                                 gene_dictionary)
            gene_out_list += get_gene_pde(global_variables, pde_Dict)
            gene_out_list += get_gene_normexp(global_variables,
                                              gene_dictionary)
            gene_out_list += get_gene_normexp_stats(global_variables,
                                                    gene_dictionary)
            gene_out_list += get_gene_annotations(global_variables,
                                                  gene_dictionary)
            out_file.write("\t".join(str(x) for x in gene_out_list) + "\n")