Visualize and annotate genomic coverage with ggplot2

HMM for annotating coding regions of DNA in S. cerevisiae chromosome III

🦀 Fqkit: A simple and cross-platform program for fastq file manipulation

[Python] Tool for calculating GC content of nucleotide sequences with optional sliding window analysis. Sequence input options include strings and the following file formats: FASTA, FASTA Nucleid Acid, GenBank, Aligned FASTA and ClustalW.

Computes gc contents in prokaryotic genomes

Sliding window program to compute the %GC in sequence of nucleotides.

List of few tools to study DNA Sequences and various operations on it. This repo can be used to solve Problems of ROSALIND (Bioinformatics Stronghold Track).

The Ribosome package is a Go library designed for efficient transcription and translation of DNA and RNA sequences, inspired by the real processes in living cells.

This project provides hands-on experience in DNA analysis using R, covering sequence manipulation, mutation analysis, GC content, fragment analysis, sequence alignment, RNA-seq, variant analysis, and phylogenetics.

A repository for my 2020-2021 AP Research project.

Bioinformatics library

a Python program to calculate GC content from fasta file

This is one of my first python scripts for a simple web-based tool that will generate basic biological data from the query DNA sequence.