nucleotides | The building blocks of JavaScript programs | Frontend Framework library

 by   davidchambers JavaScript Version: 0.4.0 License: WTFPL

kandi X-RAY | nucleotides Summary

kandi X-RAY | nucleotides Summary

nucleotides is a JavaScript library typically used in User Interface, Frontend Framework applications. nucleotides has no bugs, it has no vulnerabilities, it has a Permissive License and it has low support. You can install using 'npm i nucleotides' or download it from GitHub, npm.

The name of each mutator function is suffixed with !. This prevents unintentional mutation, draws attention to places where mutation does occur, and reserves the unsuffixed names for future use.
Support
    Quality
      Security
        License
          Reuse

            kandi-support Support

              nucleotides has a low active ecosystem.
              It has 30 star(s) with 5 fork(s). There are 5 watchers for this library.
              OutlinedDot
              It had no major release in the last 12 months.
              There are 0 open issues and 2 have been closed. On average issues are closed in 58 days. There are no pull requests.
              It has a neutral sentiment in the developer community.
              The latest version of nucleotides is 0.4.0

            kandi-Quality Quality

              nucleotides has 0 bugs and 0 code smells.

            kandi-Security Security

              nucleotides has no vulnerabilities reported, and its dependent libraries have no vulnerabilities reported.
              nucleotides code analysis shows 0 unresolved vulnerabilities.
              There are 0 security hotspots that need review.

            kandi-License License

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

            kandi-Reuse Reuse

              nucleotides releases are available to install and integrate.
              Deployable package is available in npm.
              Installation instructions are not available. Examples and code snippets are available.

            Top functions reviewed by kandi - BETA

            kandi's functional review helps you automatically verify the functionalities of the libraries and avoid rework.
            Currently covering the most popular Java, JavaScript and Python libraries. See a Sample of nucleotides
            Get all kandi verified functions for this library.

            nucleotides Key Features

            No Key Features are available at this moment for nucleotides.

            nucleotides Examples and Code Snippets

            No Code Snippets are available at this moment for nucleotides.

            Community Discussions

            QUESTION

            How to separate parts of the string with a specific percent of the needed characters?
            Asked 2021-Jun-06 at 08:09

            I'm trying to make a code for finding siRNAs. For now I've made a code that's just finding all possible siRNAs combinations. I also need to find the best ones, which must contain from 30% to 50% of the GC or CG nucleotides.

            This program is searching for the 21 nucleotides length sequences with content of CG or GC from 30 to 50%. For now, my program just generates in one string all of the possible siRNAs with length of 21, but I need to separate the ones with needed amount of GC or CG.

            Example of how my program works with K = 2, which means a length of the iRNA sequences from mRNA:

            1. inputting the DNA: ATGC
            2. It's converting to the mRNA by replacing T with U, so we get: AUGC
            3. Making a complementary chain by the Chargaff's rule, A to U, U to A, g to C, C to G, and we get: UACG
            4. Now we have a big iRNA, and now we splitting it in all possible ways for get a siRNAs, so: All iRNA combinations ['UA', 'AC', 'CG']

            And at the end I want to chose from them the ones that's content C+G nucleotides in range of 30-50%.

            Well, there we have only CG with 100, but lets change K to 4, and lets use a ATGCCGTA for the input.

            ATCGCGTA All iRNA combinations ['UAGC', 'AGCG', 'GCGC', 'CGCA', 'GCAU']

            So, here, the right ones are - UAGC and GCAU

            ...

            ANSWER

            Answered 2021-Jun-02 at 20:55

            I tried to figure out what this code does, but I couldn't)) Have you written in another language before? Just specify the input data and the output you want to receive.

            Returns true if fits the condition (30%-50%). Then you can add it to the list or whatever.

            Source https://stackoverflow.com/questions/67811950

            QUESTION

            Calculate mean only for match strings
            Asked 2021-May-31 at 19:59

            I have this assignment in which I have a file that contains alot of chromosed that I need to calculate for each one of them the mutation level. The problem is that each chromosome can appear several times and I need to find the mean for all the mutation levels of this chromosome. and on top of that i need that the mutation will be in same nucleotides (T-->C or G-->A). The mutation level is calculate by DP4 under INFO which contains four numbers that represented as [ref+,ref-,alt+,alt-] Example of the file:

            ...

            ANSWER

            Answered 2021-May-31 at 19:59

            You have lots of unnecessary for loops. The only loop you need is for the lines in the file, you don't need to loop over the characters in fields when you're splitting them or removing something from the whole field.

            At the end, you should be adding the result of the calculation to a dictionary.

            Source https://stackoverflow.com/questions/67779272

            QUESTION

            Sum iteration using r
            Asked 2021-Apr-14 at 09:26

            I have a scoring matrix called argRcount. The data is in form of a matrix where rownames indicate nucleotide names a/t/c/g and there are k = 18 columns indicating 1 to kth value of each of the nucleotide.

            I have another data (list actually) where first item contains gene-names and second item contains a vector (character) of nucleotide sequence of say n characters. In the below example n=450.

            What I actually want is to have a rolling sum for each gene, wherein first k consecutive nucleotide sequence will matched from matrix argRcount, thereafter from 2nd nucleotide to 19th, and so on for each gene. Thus in the end I will have n-k+1 values (rolling sum values) for each gene. In this particular example final outcome should have 433 values for each gene.

            These are the dput of my data:

            ...

            ANSWER

            Answered 2021-Apr-14 at 09:26

            In view of changed data in upstream BaseR strategy (without loading any extra pacakage/library)

            Source https://stackoverflow.com/questions/67086310

            QUESTION

            In Flask, is there a way to have multiple checkboxes invoke different functions on an HTML input tag?
            Asked 2021-Jan-06 at 10:18

            I have an HTML file with an input tag and two checkboxes. In a Python file I have two functions meant to act on the input tag depending on which checkbox is selected. For some reason, the function meant to calculate the gc content does not work; only the first function seems to work. How do I fix this?

            HTML Code

            ...

            ANSWER

            Answered 2021-Jan-06 at 10:18

            Ok, the whole idea needs to be-revised.

            First, You need to have two page, one for displaying the form, and the other one for showing the result.

            so you need to create two template:

            Form template (form.html)

            Source https://stackoverflow.com/questions/65567762

            QUESTION

            Group a DNA sequence in codons
            Asked 2020-Nov-30 at 20:05

            I have generated a random DNA sequence

            ...

            ANSWER

            Answered 2020-Nov-30 at 20:05

            We can use gl to create the group, and using tapply do a group by paste

            Source https://stackoverflow.com/questions/65079963

            QUESTION

            Extracting words from a complex multi-paragraph document and output them as a multiline comma separated file
            Asked 2020-Nov-01 at 15:18

            I have a document with following formatting;

            ...

            ANSWER

            Answered 2020-Oct-30 at 20:52

            A great boilerplate to start with, I prepared exact regex patterns, do the rest. PS: what you need is readlines() method + regex, no splitting!

            Source https://stackoverflow.com/questions/64612012

            QUESTION

            Fill missing values in a matrix with values from different rows in that matrix in R
            Asked 2020-Oct-28 at 12:46

            I have a matrix with nucleotide sequences (containing NAs) in rows as shown here:

            n.mat

            ...

            ANSWER

            Answered 2020-Oct-28 at 01:15

            Here's some very compact code that I will explain (and it assumes either using R v 4.x or creating the 'df' dataframe with stringsAsFactors=FALSE):

            Source https://stackoverflow.com/questions/64559653

            QUESTION

            Count the occurrences of factors per column in a matrix in R
            Asked 2020-Oct-22 at 16:55

            I have a large matrix (10000 columns and 600 rows), an example is shown below, containing nucleotides, but also NAs. I would like to count the number of occurrences of each nucleotide (factor) for each column but ignoring the NAs. The output should be in a List.

            ...

            ANSWER

            Answered 2020-Oct-22 at 16:37

            QUESTION

            Scan each column in a data frame and then change values to binary format in R
            Asked 2020-Oct-21 at 22:03

            I have a matrix with multiple individuals in rows and multiple nucleotides (values) in columns. It looks like this:

            ...

            ANSWER

            Answered 2020-Oct-21 at 22:03

            QUESTION

            How to query a region in a fasta file using biopython?
            Asked 2020-Oct-07 at 12:32

            I have a fasta file with some reference genome. I would like to obtain the reference nucleotides as a string given the chromosome, start and end indexes.

            I am looking for a function which would look like this in code:

            ...

            ANSWER

            Answered 2020-Oct-07 at 12:32

            AFAIK, biopython does not currently have this functionality. For random lookups using an index (please see samtools faidx), you'll probably want either pysam or pyfaidx. Here's an example using the pysam.FastaFile class which allows you to quickly 'fetch' sequences in a region:

            Source https://stackoverflow.com/questions/64243197

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

            Vulnerabilities

            No vulnerabilities reported

            Install nucleotides

            You can install using 'npm i nucleotides' or download it from GitHub, npm.

            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 .
            Find more information at:

            Find, review, and download reusable Libraries, Code Snippets, Cloud APIs from over 650 million Knowledge Items

            Find more libraries
            Install
          • npm

            npm i nucleotides

          • CLONE
          • HTTPS

            https://github.com/davidchambers/nucleotides.git

          • CLI

            gh repo clone davidchambers/nucleotides

          • sshUrl

            git@github.com:davidchambers/nucleotides.git

          • Stay Updated

            Subscribe to our newsletter for trending solutions and developer bootcamps

            Agree to Sign up and Terms & Conditions

            Share this Page

            share link