Update app.py
Browse files
app.py
CHANGED
|
@@ -1,6 +1,6 @@
|
|
| 1 |
import streamlit as st
|
| 2 |
import numpy as np
|
| 3 |
-
from Bio.
|
| 4 |
from hmmlearn import hmm
|
| 5 |
|
| 6 |
# Function to encode DNA sequence
|
|
@@ -8,6 +8,12 @@ def encode_sequence(seq):
|
|
| 8 |
encoding = {'A': 0, 'C': 1, 'G': 2, 'T': 3}
|
| 9 |
return np.array([encoding[base] for base in seq if base in encoding])
|
| 10 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
| 11 |
# Simple HMM model (this is a placeholder and would need proper training)
|
| 12 |
model = hmm.MultinomialHMM(n_components=2, random_state=42)
|
| 13 |
model.startprob_ = np.array([0.5, 0.5])
|
|
@@ -21,7 +27,7 @@ def analyze_dark_matter(sequence):
|
|
| 21 |
|
| 22 |
# Basic statistics
|
| 23 |
length = len(seq)
|
| 24 |
-
gc_content =
|
| 25 |
|
| 26 |
# Look for common regulatory motifs
|
| 27 |
tata_box = seq.count("TATAAA")
|
|
|
|
| 1 |
import streamlit as st
|
| 2 |
import numpy as np
|
| 3 |
+
from Bio.Seq import Seq
|
| 4 |
from hmmlearn import hmm
|
| 5 |
|
| 6 |
# Function to encode DNA sequence
|
|
|
|
| 8 |
encoding = {'A': 0, 'C': 1, 'G': 2, 'T': 3}
|
| 9 |
return np.array([encoding[base] for base in seq if base in encoding])
|
| 10 |
|
| 11 |
+
# Function to calculate GC content
|
| 12 |
+
def calculate_gc_content(seq):
|
| 13 |
+
gc_count = seq.count('G') + seq.count('C')
|
| 14 |
+
total_count = len(seq)
|
| 15 |
+
return (gc_count / total_count) * 100 if total_count > 0 else 0
|
| 16 |
+
|
| 17 |
# Simple HMM model (this is a placeholder and would need proper training)
|
| 18 |
model = hmm.MultinomialHMM(n_components=2, random_state=42)
|
| 19 |
model.startprob_ = np.array([0.5, 0.5])
|
|
|
|
| 27 |
|
| 28 |
# Basic statistics
|
| 29 |
length = len(seq)
|
| 30 |
+
gc_content = calculate_gc_content(seq)
|
| 31 |
|
| 32 |
# Look for common regulatory motifs
|
| 33 |
tata_box = seq.count("TATAAA")
|