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Visualize and annotate genomic coverage with ggplot2
🦀 Fqkit: A simple and cross-platform program for fastq file manipulation
This is one of my first python scripts for a simple web-based tool that will generate basic information from the query DNA sequence.
HMM for annotating coding regions of DNA in S. cerevisiae chromosome III
Bioinformatics library
Analysis on 5'UTRs based on sequence.
Beginner-friendly Jupyter tool to compute GC% and sliding-window profiles for DNA sequences.
A robust Python-based bioinformatics tool for comprehensive DNA sequence analysis and manipulation.
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.
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.
A Python-based tool for analyzing DNA sequences: calculates GC content, reverse complements, and detects non-overlapping open reading frames (ORFs).
Sliding window program to compute the %GC in sequence of nucleotides.
A simple Streamlit app to calculate DNA GC content 🧬
A simple Streamlit app to calculate DNA GC content 🧬
📊 Tool for analyzing and visualizing GC content in DNA sequences with FASTA input and sliding window analysis.
Computational toolkit for DNA sequence analysis.