Program for estimating πN/πS, dN/dS, and other diversity measures from next-generation sequencing data
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Updated
Aug 21, 2023 - Perl
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
A fully integrated K-mer Informed Toolkit for Bioinformatics
SEquence DAtaset builder
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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!!!
fxtools: light-weight processing tool for FASTA/FASTQ/BAM format data
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Program to clean DNA fasta sequences
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 refer…
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Performs semi-global alignments on FASTA sequences. Homework 3 for Dr. Miller's Intro to Bioinformatics class.
A small collection of one-liners in a one bash script for fasta files processing.
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