Utility to determine complementary DNA/RNA subsequences
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Updated
Jun 7, 2020 - Python
Utility to determine complementary DNA/RNA subsequences
Utility to generate codon mutations of a given coding DNA sequence
DNAc is a programming language for DNAs.
DNA sequences manipulation and analysis. Released on 2018.
Counts all SNP mutations in .map file
HCAT CLI is a command line interface tool to analyze DNA sequence data.
HCAT GUI is a visual tool to analyze and manipulate DNA sequence data.
Package to parse DNA kit files, and import them into Laravel
A library for reading and writing DNA test kit files in PHP.
fast and comprehensive k-mer counting package
Small school project to convert from DNA to mRNA to proteins using C++
R package for estimating copy-number variation from targeted DNA sequencing
Simple JS implementation of Objective Digital Stain (ODS) produces ODS images from DNA sequences. On ODSs, the information content (IC) is represented vertically on the y-axis and the frequency of different letters is represented horizontally on the x-axis.
This code generates Objective Digital Stains (ODSs) and it is implemented in PHP. On ODSs, the information content (IC) is represented vertically on the y-axis and the frequency of different letters is represented horizontally on the x-axis.
Sequence Logo - relative style is an alternative that provides full control over how the graphics of a Sequence Logo should look like, and is an alternative to an application called WebLogo. All the inner workings of this open source application are written in native javascript.
This is an application that shows the informational structure of DNA sequences. The objective digital stain (ODS) is represented by a distribution of points on a two-dimensional image, which reflects the information structure inside a DNA/RNA sequence.
Repository that has the standard DNA, RNA and Protein Objects and the standard methods to interact with them.
Various utilities for working with FASTA nucleotide sequences
Program do ustalania rozmiarów fragmentów DNA na podstawie tempa migracji na żelu (1992-94)
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