nucleotides | The building blocks of JavaScript programs | Frontend Framework library
kandi X-RAY | nucleotides Summary
kandi X-RAY | nucleotides Summary
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.
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QUESTION
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:
- inputting the DNA: ATGC
- It's converting to the mRNA by replacing T with U, so we get: AUGC
- 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
- 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 20:55I 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.
QUESTION
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 19:59You 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.
QUESTION
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 09:26In view of changed data in upstream BaseR strategy (without loading any extra pacakage/library)
QUESTION
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 10:18Ok, 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)
QUESTION
I have generated a random DNA sequence
...ANSWER
Answered 2020-Nov-30 at 20:05We can use gl
to create the group, and using tapply
do a group by paste
QUESTION
I have a document with following formatting;
...ANSWER
Answered 2020-Oct-30 at 20:52A great boilerplate to start with, I prepared exact regex patterns, do the rest. PS: what you need is readlines() method + regex, no splitting!
QUESTION
I have a matrix with nucleotide sequences (containing NAs) in rows as shown here:
n.mat
...ANSWER
Answered 2020-Oct-28 at 01:15Here'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
):
QUESTION
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 16:37like this?
QUESTION
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 22:03Here is my attempt:
QUESTION
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 12:32AFAIK, 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:
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