changes made by black

gtf_processing/pre_bedtools.py

@@ -12,22 +12,36 @@ import pandas as pd
 from gtfparse import read_gtf
 
 parser = argparse.ArgumentParser(
-    prog = 'pre_bedtools',
-    description = 'extracts ordered information from gtf file and for transcripts in the negative strand, flips the order in which exons are ordered.')
-parser.add_argument('--input_gtf_file',
-                    help='ordered and processed gtf file')
-parser.add_argument('--output_bed_file',
-                    help='bed file with only exons with strandedness taken into account')
+    prog="pre_bedtools",
+    description="extracts ordered information from gtf file and for transcripts in the negative strand, flips the order in which exons are ordered.",
+)
+parser.add_argument("--input_gtf_file", help="ordered and processed gtf file")
+parser.add_argument(
+    "--output_bed_file",
+    help="bed file with only exons with strandedness taken into account",
+)
 args = parser.parse_args()
 
 gtf = read_gtf(args.input_gtf_file)
 gtf_exons = gtf[gtf["feature"] == "exon"]
-gtf_exons = gtf_exons[["seqname", "start", "end", "transcript_id", "score", "strand", "gene_id"]]
+gtf_exons = gtf_exons[
+    ["seqname", "start", "end", "transcript_id", "score", "strand", "gene_id"]
+]
 
 gtf_df_neg = gtf_exons[gtf_exons["strand"] == "-"]
-gtf_df_neg = gtf_df_neg.sort_values(['transcript_id','start'],ascending=False).groupby('transcript_id').head(len(gtf_df_neg. transcript_id))
+gtf_df_neg = (
+    gtf_df_neg.sort_values(["transcript_id", "start"], ascending=False)
+    .groupby("transcript_id")
+    .head(len(gtf_df_neg.transcript_id))
+)
 
 gtf_df_pos = gtf_exons[gtf_exons["strand"] == "+"]
-gtf_df_pos = gtf_df_pos.sort_values(['transcript_id','start'],ascending=True).groupby('transcript_id').head(len(gtf_df_pos. transcript_id))
-
-pd.concat([gtf_df_pos, gtf_df_neg]).to_csv(args.output_bed_file,sep="\t",index=False) #gtf_df_pos and gtf_df_neg must be dataframes
+gtf_df_pos = (
+    gtf_df_pos.sort_values(["transcript_id", "start"], ascending=True)
+    .groupby("transcript_id")
+    .head(len(gtf_df_pos.transcript_id))
+)
+
+pd.concat([gtf_df_pos, gtf_df_neg]).to_csv(
+    args.output_bed_file, sep="\t", index=False
+)  # gtf_df_pos and gtf_df_neg must be dataframes

sequence_extractor/cli.py

@@ -5,15 +5,15 @@ from exon_concatenation import exon_concatenation
 from poly_a import poly_a_addition_to_fasta_list
 
 parser = argparse.ArgumentParser(
-    prog = 'transcript_sequence_extractor',
-    description = 'extracts transcript sequences from genome sequence and ouputs transcripts with PolyA tail added to them')
-parser.add_argument('--input_fasta_file',
-                    help='fasta file obtained from bedtools')
-parser.add_argument('--output_file_name',
-                    help='Name of the output fasta file')
+    prog="transcript_sequence_extractor",
+    description="extracts transcript sequences from genome sequence and ouputs transcripts with PolyA tail added to them",
+)
+parser.add_argument("--input_fasta_file", help="fasta file obtained from bedtools")
+parser.add_argument("--output_file_name", help="Name of the output fasta file")
 
 args = parser.parse_args()
 
+
 def main():
     """Runs on the output from bedtools and concatenates the exons together and adds a polyA tail and outputs a fasta file.
 
@@ -26,11 +26,12 @@ def main():
     LOG.info("sequence_extractor begins")
     fasta_list = exon_concatenation(args.input_fasta_file)
     final_list = poly_a_addition_to_fasta_list(fasta_list)
-    with open(args.output_file_name, 'w', encoding="utf-8") as fasta_out:
-        fasta_out.write('\n'.join('%s\n%s' % x for x in final_list))
+    with open(args.output_file_name, "w", encoding="utf-8") as fasta_out:
+        fasta_out.write("\n".join("%s\n%s" % x for x in final_list))
     LOG.info("sequence_extractor ends")
 
-if ___name__ == 'main':
+
+if ___name__ == "main":
     logging.basicConfig(
         format='[%(asctime)s: %(levelname)s] %(message)s (module "%(module)s")',
         level=logging.INFO,

sequence_extractor/exon_concatenation.py

 """Script containing the function to concatenate exons and output the results in a list of tuples"""
+
+
 def exon_concatenation(
     post_bedtools_fasta: str,
 ) -> list:
@@ -10,7 +12,7 @@ def exon_concatenation(
     Returns:
         A list containing transcript ID and concatenated exons in tuples.
     """
-    with open(post_bedtools_fasta,'r', encoding="utf-8") as fasta:
+    with open(post_bedtools_fasta, "r", encoding="utf-8") as fasta:
         annotation = []
         fasta_format_list = []
         for line1, line2 in zip(fasta, fasta):

sequence_extractor/poly_a.py

 """ This script contains two functions and the first function is called by the second function and used to add poly A tail to the concatenated exon"""
 import numpy as np
+
 # To do: Taking probabilities of nucleotides from user and raising error if sum != 1
 def poly_a_generator(
     exon: str,
@@ -12,10 +13,13 @@ def poly_a_generator(
     Returns:
             RNA with polyA tail added to its 3' end.
     """
-    list_of_nucleotides = ['A','T','G','C']
-    poly_a_string = ''.join(np.random.choice(list_of_nucleotides,250,p=[0.914,0.028,0.025,0.033]))
+    list_of_nucleotides = ["A", "T", "G", "C"]
+    poly_a_string = "".join(
+        np.random.choice(list_of_nucleotides, 250, p=[0.914, 0.028, 0.025, 0.033])
+    )
     return exon + poly_a_string
 
+
 def poly_a_addition_to_fasta_list(
     fasta_list: list,
 ) -> list: