From 7d9f2581ceba92ac9a880b6c47883d83d82af18b Mon Sep 17 00:00:00 2001
From: "hugo.madgeleon" <hugo.madgeleon@stud.unibas.ch>
Date: Wed, 7 Dec 2022 09:11:16 +0100
Subject: [PATCH] remove old code
---
frag_package/fragmentation.py | 100 ++++++++++++++++++++-----------
frag_package/fragmentation_v2.py | 64 --------------------
2 files changed, 64 insertions(+), 100 deletions(-)
delete mode 100644 frag_package/fragmentation_v2.py
diff --git a/frag_package/fragmentation.py b/frag_package/fragmentation.py
index 7dba609..80762e2 100644
--- a/frag_package/fragmentation.py
+++ b/frag_package/fragmentation.py
@@ -1,36 +1,64 @@
-import random
-
-
-dna_seq = {
- "ATAACATGTGGATGGCCAGTGGTCGGTTGTTACACGCCTACCGCGATGCTGAATGACCCGGACTAGAGTGGCGAAATTTATGGCGTGTGACCCGTTATGC": 100,
- "TCCATTTCGGTCAGTGGGTCATTGCTAGTAGTCGATTGCATTGCCATTCTCCGAGTGATTTAGCGTGACAGCCGCAGGGAACCCATAAAATGCAATCGTA": 100
-}
-
-mean_length = 12
-std = 1
-
-term_frags = []
-for seq, counts in dna_seq.items():
- for _ in range(counts):
- n_cuts = int(len(seq)/mean_length)
- cuts = random.sample(range(1,len(seq)-1), n_cuts)
- cuts.sort()
- cuts.insert(0,0)
- term_frag = ""
- for i, val in enumerate(cuts):
- if i == len(cuts)-1:
- fragment = seq[val:cuts[-1]]
- else:
- fragment = seq[val:cuts[i+1]]
- if mean_length-std <= len(fragment) <= mean_length+std:
- term_frag = fragment
- if term_frag == "":
- continue
- else:
- term_frags.append(term_frag)
-
-with open('terminal_frags.txt', 'w') as f:
- for line in term_frags:
- f.write(line)
- f.write('\n')
-
+import re
+
+import numpy as np
+import pandas as pd
+
+
+def fasta_process(fasta_file):
+ with open(fasta_file, "r") as f:
+ lines = f.readlines()
+
+ ident_pattern = re.compile('>(\S+)')
+ seq_pattern = re.compile('^(\S+)$')
+
+ genes = {}
+ for line in lines:
+ if ident_pattern.search(line):
+ seq_id = (ident_pattern.search(line)).group(1)
+ elif seq_id in genes.keys():
+ genes[seq_id] += (seq_pattern.search(line)).group(1)
+ else:
+ genes[seq_id] = (seq_pattern.search(line)).group(1)
+ return genes
+
+def fragmentation(fasta_file, counts_file, mean_length, std, a_prob, t_prob, g_prob, c_prob):
+ fasta = fasta_process(fasta_file)
+ seq_counts = pd.read_csv(counts_file, names = ["seqID", "count"])
+
+ # nucs = ['A','T','G','C']
+ # mononuc_freqs = [0.22, 0.25, 0.23, 0.30]
+ nuc_probs = {'A':a_prob, 'T':t_prob, 'G':g_prob, 'C':c_prob} # calculated using https://www.nature.com/articles/srep04532#MOESM1
+
+ term_frags = []
+ for seq_id, seq in fasta.items():
+ counts = seq_counts[seq_counts["seqID"] == seq_id]["count"]
+ for _ in range(counts):
+ n_cuts = int(len(seq)/mean_length)
+
+ # non-uniformly random DNA fragmentation implementation based on https://www.nature.com/articles/srep04532#Sec1
+ # assume fragmentation by sonication for NGS workflow
+ cuts = []
+ cut_nucs = np.random.choice(list(nuc_probs.keys()), n_cuts, p=list(nuc_probs.values()))
+ for nuc in cut_nucs:
+ nuc_pos = [x.start() for x in re.finditer(nuc, seq)]
+ pos = np.random.choice(nuc_pos)
+ while pos in cuts:
+ pos = np.random.choice(nuc_pos)
+ cuts.append(pos)
+
+ cuts.sort()
+ cuts.insert(0,0)
+ term_frag = ""
+ for i, val in enumerate(cuts):
+ if i == len(cuts)-1:
+ fragment = seq[val+1:cuts[-1]]
+ else:
+ fragment = seq[val:cuts[i+1]]
+ if mean_length-std <= len(fragment) <= mean_length+std:
+ term_frag = fragment
+ if term_frag == "":
+ continue
+ else:
+ term_frags.append(term_frag)
+ return term_frags
+
diff --git a/frag_package/fragmentation_v2.py b/frag_package/fragmentation_v2.py
deleted file mode 100644
index 80762e2..0000000
--- a/frag_package/fragmentation_v2.py
+++ /dev/null
@@ -1,64 +0,0 @@
-import re
-
-import numpy as np
-import pandas as pd
-
-
-def fasta_process(fasta_file):
- with open(fasta_file, "r") as f:
- lines = f.readlines()
-
- ident_pattern = re.compile('>(\S+)')
- seq_pattern = re.compile('^(\S+)$')
-
- genes = {}
- for line in lines:
- if ident_pattern.search(line):
- seq_id = (ident_pattern.search(line)).group(1)
- elif seq_id in genes.keys():
- genes[seq_id] += (seq_pattern.search(line)).group(1)
- else:
- genes[seq_id] = (seq_pattern.search(line)).group(1)
- return genes
-
-def fragmentation(fasta_file, counts_file, mean_length, std, a_prob, t_prob, g_prob, c_prob):
- fasta = fasta_process(fasta_file)
- seq_counts = pd.read_csv(counts_file, names = ["seqID", "count"])
-
- # nucs = ['A','T','G','C']
- # mononuc_freqs = [0.22, 0.25, 0.23, 0.30]
- nuc_probs = {'A':a_prob, 'T':t_prob, 'G':g_prob, 'C':c_prob} # calculated using https://www.nature.com/articles/srep04532#MOESM1
-
- term_frags = []
- for seq_id, seq in fasta.items():
- counts = seq_counts[seq_counts["seqID"] == seq_id]["count"]
- for _ in range(counts):
- n_cuts = int(len(seq)/mean_length)
-
- # non-uniformly random DNA fragmentation implementation based on https://www.nature.com/articles/srep04532#Sec1
- # assume fragmentation by sonication for NGS workflow
- cuts = []
- cut_nucs = np.random.choice(list(nuc_probs.keys()), n_cuts, p=list(nuc_probs.values()))
- for nuc in cut_nucs:
- nuc_pos = [x.start() for x in re.finditer(nuc, seq)]
- pos = np.random.choice(nuc_pos)
- while pos in cuts:
- pos = np.random.choice(nuc_pos)
- cuts.append(pos)
-
- cuts.sort()
- cuts.insert(0,0)
- term_frag = ""
- for i, val in enumerate(cuts):
- if i == len(cuts)-1:
- fragment = seq[val+1:cuts[-1]]
- else:
- fragment = seq[val:cuts[i+1]]
- if mean_length-std <= len(fragment) <= mean_length+std:
- term_frag = fragment
- if term_frag == "":
- continue
- else:
- term_frags.append(term_frag)
- return term_frags
-
--
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