diff options
author | BonfaceKilz | 2021-04-30 12:16:51 +0300 |
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committer | BonfaceKilz | 2021-04-30 13:45:15 +0300 |
commit | c7e661b8ff9f70955418fbc4527378904beb0cf4 (patch) | |
tree | 7a164b42d46e15b6f2775a50137b412c8713e2f3 /wqflask/utility/gen_geno_ob.py | |
parent | 385da724b63f57d0fb1bbe3476cea31ef837c081 (diff) | |
download | genenetwork2-c7e661b8ff9f70955418fbc4527378904beb0cf4.tar.gz |
autopep8: Fix E20-E27
Run:
python -m autopep8 --in-place --recrusive ./ --select\
E20,E211,E22,E224,E224,E225,E226,E227,E228,E231,E241,\
E242,E251,E252,E26,E265,E266,E27 -p 3
Diffstat (limited to 'wqflask/utility/gen_geno_ob.py')
-rw-r--r-- | wqflask/utility/gen_geno_ob.py | 18 |
1 files changed, 9 insertions, 9 deletions
diff --git a/wqflask/utility/gen_geno_ob.py b/wqflask/utility/gen_geno_ob.py index 0a381c9b..9cfa39f9 100644 --- a/wqflask/utility/gen_geno_ob.py +++ b/wqflask/utility/gen_geno_ob.py @@ -1,5 +1,5 @@ import utility.logger -logger = utility.logger.getLogger(__name__ ) +logger = utility.logger.getLogger(__name__) class genotype: """ @@ -18,7 +18,7 @@ class genotype: self.filler = False self.mb_exists = False - #ZS: This is because I'm not sure if some files switch the column that contains Mb/cM positions; might be unnecessary + # ZS: This is because I'm not sure if some files switch the column that contains Mb/cM positions; might be unnecessary self.cm_column = 2 self.mb_column = 3 @@ -36,14 +36,14 @@ class genotype: return len(self.chromosomes) def read_rdata_output(self, qtl_results): - #ZS: This is necessary because R/qtl requires centimorgan marker positions, which it normally gets from the .geno file, but that doesn't exist for HET3-ITP (which only has RData), so it needs to read in the marker cM positions from the results - self.chromosomes = [] #ZS: Overwriting since the .geno file's contents are just placeholders + # ZS: This is necessary because R/qtl requires centimorgan marker positions, which it normally gets from the .geno file, but that doesn't exist for HET3-ITP (which only has RData), so it needs to read in the marker cM positions from the results + self.chromosomes = [] # ZS: Overwriting since the .geno file's contents are just placeholders - this_chr = "" #ZS: This is so it can track when the chromosome changes as it iterates through markers + this_chr = "" # ZS: This is so it can track when the chromosome changes as it iterates through markers chr_ob = None for marker in qtl_results: locus = Locus(self) - if (str(marker['chr']) != this_chr) and this_chr != "X": #ZS: This is really awkward but works as a temporary fix + if (str(marker['chr']) != this_chr) and this_chr != "X": # ZS: This is really awkward but works as a temporary fix if this_chr != "": self.chromosomes.append(chr_ob) this_chr = str(marker['chr']) @@ -68,7 +68,7 @@ class genotype: with open(filename, 'r') as geno_file: lines = geno_file.readlines() - this_chr = "" #ZS: This is so it can track when the chromosome changes as it iterates through markers + this_chr = "" # ZS: This is so it can track when the chromosome changes as it iterates through markers chr_ob = None for line in lines: if line[0] == "#": @@ -141,7 +141,7 @@ class Chr: self.loci.append(Locus(self.geno_ob, marker_row)) class Locus: - def __init__(self, geno_ob, marker_row = None): + def __init__(self, geno_ob, marker_row=None): self.chr = None self.name = None self.cM = None @@ -175,5 +175,5 @@ class Locus: for allele in marker_row[start_pos:]: if allele in list(geno_table.keys()): self.genotype.append(geno_table[allele]) - else: #ZS: Some genotype appears that isn't specified in the metadata, make it unknown + else: # ZS: Some genotype appears that isn't specified in the metadata, make it unknown self.genotype.append("U") |