ccg | Generate scaffolds/models for FastAPI and Tortoise ORM | Generator Utils library
kandi X-RAY | ccg Summary
kandi X-RAY | ccg Summary
ccg is a cli generator that generates boilerplate code. It currently only supports model generation for tortoise orm.
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QUESTION
Im currently working on a study project where I am to make a python program where I can enter a DNA sequence, get all the possible reading frames from it and then find any open reading frame. I can't use Biopython as we are to do this ourselves.
From the code I have written, I will get an output in the style of:
["TGC", "ATG", "ATA", "TGG", "AGG", "AGG", "CCG", TAA", "TAG", "TGA"]
What I want to do now is to define the start codon as "ATG" and get its index as well as define stop codons as ["TAA", "TAG", "TGA"]
and if any of these three are found, the index of the first found is reported and the rest is ignored. And if no stop codon is found to return some string.
In addition to this, i want to be able to compare the "lengts" of up to 6 different input in the style mentioned above and chone the one which is the longest.
This is my first time posting here so appologies if the question is not well phrased and thanks for any help!
...ANSWER
Answered 2021-May-17 at 18:00I am not completely sure if this is what you want, but to find the first occurrence of strings in a longer string you can do like this for example
QUESTION
I am trying to write a fuction that translates an mRNA sequence to a peptide sequence depending on the nucleotide from which we start counting codons (either the first nucleotide, the second or the third). I have a code for it, but when I print the three results (of the three peptides) I only get a sequence for the first peptide. The last two are blank. Any idea what the problem might be? And how could I return all three peptides by default?
...ANSWER
Answered 2021-May-08 at 17:11It always return after first if check. It should be:
QUESTION
Hello I am looking to do find out this:
Assume I have this.
...ANSWER
Answered 2021-Apr-26 at 15:58If a
and b
are your inputs from question:
QUESTION
I had no error. Always refresh cache and local memory.
Resources for Verifying Translations:
[NCBI Protein Translation Tool][1] (Validation)
[Text Compare][2] (Verification)
[Solution Inspiration][3]
300 DNA chars -> 100 protein chars.
...ANSWER
Answered 2021-Mar-31 at 09:38I think the issue is with you mixing up variable names - your translation code appends to protein
but you print output_protein
which I assume is actually created somewhere else in your code(?). Also, you first edit the variable dna_sequence
but iterate over dna
which I assume is also defined elsewhere and maybe doesn't match dna_sequence
.
After editing the variable names I can use your code to get the same translation as the NCBI tool.
QUESTION
I have a list of pandas data frames that I got applying the groupby function and I want to add to them a new column with the frequency of each kmer. I did that with a loop but I got a message warning that I need to use df.loc[index, col_names]. Here it is a link to one example of the csv file: https://drive.google.com/file/d/17vYbIEza7l-1mFnavGGO1QjCjPdhxG7C/view?usp=sharing
...ANSWER
Answered 2021-Apr-05 at 12:28It's an error related SettingWithCopyWarning. It's important — read up on it here. Usually you can avoid it with .loc
and by avoiding repeat-slicing, but in some cases where you have to slice repeatedly you can get around it by ending .copy()
to the end of the expression. You can learn when and why this is important via the link. For a more precise answer for how this is emerging from you'll code, you'll need to show us an MRCE of your code.
QUESTION
def amino_acids(mrna):
aa_dict = {'CUU': 'Leu', 'UAG': '---', 'ACA': 'Thr', 'AAA': 'Lys', 'AUC': 'Ile',
'AAC': 'Asn','AUA': 'Ile', 'AGG': 'Arg', 'CCU': 'Pro', 'ACU': 'Thr',
'AGC': 'Ser','AAG': 'Lys', 'AGA': 'Arg', 'CAU': 'His', 'AAU': 'Asn',
'AUU': 'Ile','CUG': 'Leu', 'CUA': 'Leu', 'CUC': 'Leu', 'CAC': 'His',
'UGG': 'Trp','CAA': 'Gln', 'AGU': 'Ser', 'CCA': 'Pro', 'CCG': 'Pro',
'CCC': 'Pro', 'UAU': 'Tyr', 'GGU': 'Gly', 'UGU': 'Cys', 'CGA': 'Arg',
'CAG': 'Gln', 'UCU': 'Ser', 'GAU': 'Asp', 'CGG': 'Arg', 'UUU': 'Phe',
'UGC': 'Cys', 'GGG': 'Gly', 'UGA':'---', 'GGA': 'Gly', 'UAA': '---',
'ACG': 'Thr', 'UAC': 'Tyr', 'UUC': 'Phe', 'UCG': 'Ser', 'UUA': 'Leu',
'UUG': 'Leu', 'UCC': 'Ser', 'ACC': 'Thr', 'UCA': 'Ser', 'GCA': 'Ala',
'GUA': 'Val', 'GCC': 'Ala', 'GUC': 'Val', 'GGC':'Gly', 'GCG': 'Ala',
'GUG': 'Val', 'GAG': 'Glu', 'GUU': 'Val', 'GCU': 'Ala', 'GAC': 'Asp',
'CGU': 'Arg', 'GAA': 'Glu', 'AUG': 'Met', 'CGC': 'Arg'}
mrna_list = [aa_dict[mrna[i:i + 3]] for i in range(0, len(mrna) - 1, 3)]
count = 0
while True:
if mrna_list[count] == '---':
mrna_list = mrna_list[:count]
break
else:
count += 1
conversion_result = tuple(mrna_list)
return [conversion_result, count]
...ANSWER
Answered 2021-Mar-24 at 18:27To get only the unique elements of a list, you can usually just convert it to a set
and back (at least, when it only contains simple things like strings or numbers). You can then find the number of unique elements by taking the length of that set:
QUESTION
This post is related to my previous question about string splitting: Awk split string into words and numbers. Let's say we have a following string:
...ANSWER
Answered 2021-Mar-05 at 17:55% echo 1A5T4 | gawk 'BEGIN{ FS=""; }{ for (i=1;i<=NF;i++) { if($i>="A"){ s=s $i } else { for(j=1;j<=$i;j++)s=s "." }} print s }'
.A.....T....
% echo 1A2^CCG3T4 | gawk 'BEGIN{ FS=""; }{ for (i=1;i<=NF;i++) { if($i>="A"){ s=s $i } else { for(j=1;j<=$i;j++)s=s "." }} print s }'
.A..^CCG...T....
%
QUESTION
As I was bored and wanted to practice my python, I thought I'd write a script that took some genetic code and converted it into the amino acid sequence. It looks through the code one letter at a time and when it sees a certain sequence, starts translating triplets of genetic code into their equivalent amino acid and strings them together until it reaches a triplet of genetic code that doesn't encode an amino acid. The script then goes back to where it started this translation, and restarts iterating through the code until it finds another start sequence.
The script works, up to a point. I started off using a while loop to iterate through the triplets of genetic code after a start sequence, but when it reaches the end of the genetic code, it goes out of range:
...ANSWER
Answered 2021-Feb-24 at 20:38You keep incrementing base
and incrementing l
but without checking if you've exceeded the length of the rna string. Changing the condition of your while loop to
QUESTION
I'm having some trouble with this code, I have used something similar before and is working but it isn't on this one I don't know why. Each time I hit submit the object message comes empty, the only values that are submitted into the database are the ones that I add in the controller like the Date for example, I don't know much about ASP.NET to know why is it failing nor the correct terms to look for myself on google
Model
...ANSWER
Answered 2021-Jan-16 at 01:30I'm pretty sure uou need to make those fields into properties by adding get
and set
methods.
e.g.
QUESTION
i have a protein sequence:
...ANSWER
Answered 2021-Jan-04 at 19:54import itertools
list_codons = [('ATT', 'ATC', 'ATA'),
('GAA', 'GAG'),
('GAA', 'GAG'),
('GCT', 'GCC', 'GCA', 'GCG'),
('ACT', 'ACC', 'ACA', 'ACG'),
('CAT', 'CAC'),
('ATG',),
('ACT', 'ACC', 'ACA', 'ACG'),
('CCT', 'CCC', 'CCA', 'CCG'),
('TGT', 'TGC'),
('TAT', 'TAC'),
('GAA', 'GAG'),
('TTA', 'TTG', 'CTT', 'CTC', 'CTA', 'CTG'),
('CAT', 'CAC'),
('GGT', 'GGC', 'GGA', 'GGG'),
('TTA', 'TTG', 'CTT', 'CTC', 'CTA', 'CTG'),
('CGT', 'CGC', 'CGA', 'CGG', 'AGA', 'AGG'),
('TGG',),
('GTT', 'GTC', 'GTA', 'GTG'),
('CAA', 'CAG'),
('ATT', 'ATC', 'ATA'),
('CAA', 'CAG'),
('GAT', 'GAC'),
('TAT', 'TAC'),
('GCT', 'GCC', 'GCA', 'GCG'),
('ATT', 'ATC', 'ATA'),
('AAT', 'AAC'),
('GTT', 'GTC', 'GTA', 'GTG'),
('ATG',),
('CAA', 'CAG'),
('TGT', 'TGC'),
('TTA', 'TTG', 'CTT', 'CTC', 'CTA', 'CTG')]
counter = 0; max_proc = 1000000; list_seq = []
for x in itertools.product(*list_codons):
counter += 1
if counter % max_proc == 0:
#Do your stuff by slice and clear the list
list_seq = []
list_seq.append(x)
print (counter)
print (x)
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You can use ccg like any standard Python library. You will need to make sure that you have a development environment consisting of a Python distribution including header files, a compiler, pip, and git installed. Make sure that your pip, setuptools, and wheel are up to date. When using pip it is generally recommended to install packages in a virtual environment to avoid changes to the system.
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