GAG | Generates an NCBI .tbl file of annotations on a genome | Genomics library

 by   genomeannotation Python Version: v2.0.1 License: MIT

kandi X-RAY | GAG Summary

kandi X-RAY | GAG Summary

GAG is a Python library typically used in Artificial Intelligence, Genomics applications. GAG has no bugs, it has no vulnerabilities, it has a Permissive License and it has low support. However GAG build file is not available. You can download it from GitHub.

A command line program to read, modify, annotate and output genomic data. Can write files to .gff3 or to the NCBI's .tbl format. Perfect if you're trying to submit a genome to NCBI. For usage, type 'python gag.py'. See documentation at Please cite the following: when using GAG for your research.
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            kandi-support Support

              GAG has a low active ecosystem.
              It has 53 star(s) with 15 fork(s). There are 14 watchers for this library.
              OutlinedDot
              It had no major release in the last 12 months.
              There are 14 open issues and 167 have been closed. On average issues are closed in 308 days. There are no pull requests.
              It has a neutral sentiment in the developer community.
              The latest version of GAG is v2.0.1

            kandi-Quality Quality

              GAG has no bugs reported.

            kandi-Security Security

              GAG has no vulnerabilities reported, and its dependent libraries have no vulnerabilities reported.

            kandi-License License

              GAG is licensed under the MIT License. This license is Permissive.
              Permissive licenses have the least restrictions, and you can use them in most projects.

            kandi-Reuse Reuse

              GAG releases are available to install and integrate.
              GAG has no build file. You will be need to create the build yourself to build the component from source.

            Top functions reviewed by kandi - BETA

            kandi has reviewed GAG and discovered the below as its top functions. This is intended to give you an instant insight into GAG implemented functionality, and help decide if they suit your requirements.
            • Perform the gag
            • Add a genome from a file
            • Read an annotation file
            • Apply a filter
            • Update a GFF file based on trimlist
            • Checks if two indices are within the range
            • Check if intervals overlap
            • Updates an agp file
            • Return a dictionary of information about the CDS
            • Return a dictionary containing the partial info for each gene
            • Return a string representation of this gene
            • Calculate statistics on the genome
            • Adjust the indices by n
            • Return the index of the first exon
            • Parses a string into a list of regions
            • Returns the length of the longest exon
            • Returns the total length of the exon
            • Returns the total number ofags in the mRNA
            • Produce a table of nucleotides
            • Convert cds to table
            • Create start and stop coordinates for all mrna
            • Add the annotations from the given annotations
            • Remove features from bad list
            • Return the length of the segment
            • Convert to protein sequence
            • Convert the mrna sequence to a cds file
            Get all kandi verified functions for this library.

            GAG Key Features

            No Key Features are available at this moment for GAG.

            GAG Examples and Code Snippets

            No Code Snippets are available at this moment for GAG.

            Community Discussions

            QUESTION

            Function converting mRNA to peptide sequence depending on the reading frame does not work correctly
            Asked 2021-May-08 at 17:11

            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 17:11

            It always return after first if check. It should be:

            Source https://stackoverflow.com/questions/67450015

            QUESTION

            Python dictionary match any element of key
            Asked 2021-Apr-27 at 05:20

            If one has a dict like the following:

            ...

            ANSWER

            Answered 2021-Apr-25 at 21:38

            No there isn't. Instead, use an alternative form to you dictionary, it's ok to have duplicate values so:

            Source https://stackoverflow.com/questions/67258010

            QUESTION

            DNA to Protein | translation incorrection
            Asked 2021-Apr-22 at 15:41

            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 09:38

            I 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.

            Source https://stackoverflow.com/questions/66884855

            QUESTION

            Fuzzy regex: fuzzy count for substitution is always 1
            Asked 2021-Apr-11 at 16:02

            I am using the Python regex module for approximate string matching. I have a DNA sequence which I would like to search for a specific pattern, while allowing for at most 1 substitution: {s<=1}. In the DNA sequence, multiple patterns are acceptable. For example, the first three characters can either be 'GAG' or 'GAT', and the same principle holds true for the rest of the DNA sequence.

            I made an example below, where I want to use regex search on a 9 character long string. To my understanding, the pattern should match the string without any subtitution.

            However, regex gives me a match with a fuzzy count of 1 for substitutions (see below). I do not understand this, as the sequence matches the pattern.

            ...

            ANSWER

            Answered 2021-Apr-11 at 15:55

            From the regex module documentation:

            By default, fuzzy matching searches for the first match that meets the given constraints.

            In your case, the first match is obtained using GAG and performing one substitution (since GAG is tried before GAT). You can use the BESTMATCH flag to look for the best match instead:

            Source https://stackoverflow.com/questions/67046514

            QUESTION

            I have a list of df resulting by groupby and I need to add a new column with the frequency of kmers
            Asked 2021-Apr-05 at 12:28

            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 12:28

            It'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.

            Source https://stackoverflow.com/questions/66936330

            QUESTION

            How to extract the data from a column with priority order given in another file?
            Asked 2021-Mar-31 at 22:25

            I have two dataframes

            df1

            ...

            ANSWER

            Answered 2021-Mar-31 at 22:25

            QUESTION

            Creating an dropdown menu using a Vue instance
            Asked 2021-Mar-30 at 22:50

            I switched from React to Vue and for me there are some incomprehensible nuances I want to create a drop-down menu, but I have some incomprehensible things related to this who is familiar with React knows that you can create a certain property with a boolean value inside a state or using hooks then when clicking on the buttons, use setState and manage with it,

            I understand that you can implement something like this in Vue JS, but I am confused by one question, how can you create a certain property in Vue JS? is it possible to instantiate by type let app = new Vue({el: '#app',}); for each component? Because I don't understand how to create a property for example showDropDown without using new Vue ({})?

            My code at the moment looks like this

            ...

            ANSWER

            Answered 2021-Mar-30 at 22:50

            Using the Options API, you can create local reactive state in Vue components by declaring them in data:

            Source https://stackoverflow.com/questions/66879261

            QUESTION

            Struggling to find the number of distinct amino acids
            Asked 2021-Mar-24 at 18:27
            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 18:27

            To 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:

            Source https://stackoverflow.com/questions/66786981

            QUESTION

            How can I stop my script going out of range?
            Asked 2021-Feb-24 at 20:38

            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 20:38

            You 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

            Source https://stackoverflow.com/questions/66358276

            QUESTION

            calculate all possible combinations of RNA codons for a protein sequence
            Asked 2021-Jan-04 at 22:50

            i have a protein sequence:

            ...

            ANSWER

            Answered 2021-Jan-04 at 19:54
            import 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)
            

            Source https://stackoverflow.com/questions/65568728

            Community Discussions, Code Snippets contain sources that include Stack Exchange Network

            Vulnerabilities

            No vulnerabilities reported

            Install GAG

            You can download it from GitHub.
            You can use GAG 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.

            Support

            For any new features, suggestions and bugs create an issue on GitHub. If you have any questions check and ask questions on community page Stack Overflow .
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