Visualize and annotate genomic coverage with ggplot2

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

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

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

Bioinformatics library

My solutions for rosalind problems

Computes gc contents in prokaryotic genomes

Beginner-friendly Jupyter tool to compute GC% and sliding-window profiles for DNA sequences.

Computational toolkit for DNA sequence analysis.

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

A Python-based tool for analyzing DNA sequences: calculates GC content, reverse complements, and detects non-overlapping open reading frames (ORFs).

[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.

A simple Streamlit app to calculate DNA GC content 🧬

📊 Tool for analyzing GC content in DNA sequences with FASTA input and sliding window analysis.

a Python program to calculate GC content from fasta file

A repository for my 2020-2021 AP Research project.

A simple Streamlit app to calculate DNA GC content 🧬

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 robust Python-based bioinformatics tool for comprehensive DNA sequence analysis and manipulation.