There are 1 repository under fasta-sequences topic.
Program for estimating πN/πS, dN/dS, and other diversity measures from next-generation sequencing data
FluentDNA allows you to browse sequence data of any size using a zooming visualization similar to Google Maps. You can use FluentDNA as a standalone program or as a python module for your own bioinformatics projects.
genomic alignment similarity search tool
Evolutionary Bioinformatics Toolkit (EBT)
Split multi fasta file into single fasta files
A naive implementation of a k-mer counter in Python, takes fasta files and k-mer length requests and outputs all k-mers of length k, their reverse complement, and their frequency within their respective sequence for each sequence in the file.
Shuffle the string sequences such that the k-mer frequency is preserved in each string
SEquence DAtaset builder
Sequence clustering and database creation using mmseqs, from local fasta files
A tool for manipulating fasta files and obtaining new sequence data from NCBI in fasta format
Computational programs and algorithms used to convert information from biochemical experiments (DNA/RNA/Protein/DNA chip/NGS) into useful information and data.
Program to clean DNA fasta sequences
A tool for predicting the effects of missense mutations on protein stability changes upon missense mutation using protein sequence only.
Team Genomics One is a group of Bioinformatics enthusiasts gathered together from around the globe , to learn and move forward in solving biological myths by analyzing various types of biological data. We believe Team Work is Dream Work!!!
Removes duplicate sequences in multifasta file
omicR It creates fasta files, downloads genomes from NCBI using the refseq number, creates databases to run BLAST+, runs BLAST+ and filters these results to obtain the best match per sequence. These scripts can be used to run BLAST alignment of short-read (DArTseq data). It only works with BLAST V 2.7 or under.
omicR for R studio creates fasta files, downloads genomes from NCBI using the refseq number, creates databases to run BLAST+, runs BLAST+ and filters these results to obtain the best match per sequence. These scripts can be used to run BLAST alignment of short-read (DArTseq data) and long-read sequences (Illumina, PacBio… etc). You can use reference genomes from NCBI, or any other genetic sequence that you would like to use as reference.
A small collection of one-liners in a one bash script for fasta files processing.
A small fasta CLI toolkit developed in Rust
Performs semi-global alignments on FASTA sequences. Homework 3 for Dr. Miller's Intro to Bioinformatics class.
Terminal App to find ORF
simple and convenient program to convert fasta sequences to fastq sequences
An R script that calculates a similarity matrix for a list of protein sequences with the aid of Bleakley-Yamanishi Normalized Smith-Waterman Similarity Score.
SeqCutter is designed to extract specific subsequences from a FASTA file based on a cluster definition.
Plasmidome analysis to track the transfer route of AMR genes in bacteria
Various utilities for working with FASTA nucleotide sequences
Creating plots using FASTA amino-acid files
Reads a protein FASTA file and filters the proteins by organism name, protein name, or taxonomy ID to create a new, filtered file.
Team Genomics One is a group of Bioinformatics enthusiasts gathered together from around the globe , to learn and move forward in solving biological myths by analyzing various types of biological data. We believe Team Work is Dream Work!!!
Analysis of FASTA ,Protein,DNA sequence.
🧬 Implementation of the Smith-Waterman algorithm for aligning amino acid sequences.
Read a fasta sequence file, calculate base counts, print calculated base counts and print sequence length.
Miscellaneous Scripts in Bioinformatics