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

Computes gc contents in prokaryotic genomes

Analysis on 5'UTRs based on sequence.

My solutions for rosalind problems

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

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

Computational toolkit for DNA sequence analysis.

Bioinformatics end-semester project using k-mer and GC-content features with K-Means clustering to identify candidate functional non-coding RNA patterns from genomic sequence data, with miRNA-based comparative analysis.

Python tool to compute GC content for DNA sequences, export results to CSV, and visualize them through simple bar plots.

A simple Streamlit app to calculate DNA GC content 🧬

a Python program to calculate GC content from fasta file

[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 repository for my 2020-2021 AP Research project.

Analysis of stress- and epigenetics-related genes using real multi-FASTA data (GC%, heatmap, boxplot, Biopython & Pandas).

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

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.