Bioinformatics Tool
Browse 19 websites in this category
Sites where Bioinformatics Tool is a core feature are shown first, marked with a Core badge.
BioCyc offers integrated genome and metabolic pathway data for thousands of organisms, plus bioinformatics tools for research and analysis.
Explore open-source tools, libraries, and file format specs for next-generation DNA sequencing developers, including C and Java APIs from Samtools.
Samtools offers a suite of open-source tools for working with high-throughput sequencing data, helping researchers process and analyze genomic datasets.
Bowtie offers a fast and efficient tool for aligning short DNA sequences to genomes, making it easier for researchers to analyze large-scale genetic data.
Burrows-Wheeler Aligner (BWA) is a software tool for mapping DNA sequences to reference genomes, supporting both short and long read alignment.
Access information and downloads for older versions of SAMtools, a toolkit for working with DNA sequencing data in bioinformatics projects.
Jalview is a free program for editing, visualizing, and analyzing multiple sequence alignments, offering tools for phylogenetic trees and molecular structures.
Genome Modeling Tools offers resources and downloads for genomic data analysis, including support for TIGRA-SV and related research tools.
Explore detailed documentation for bcbio-nextgen, a Python toolkit offering automated pipelines for high-throughput sequencing analysis in bioinformatics.
Cutadapt's documentation helps you use this tool to trim adapters and unwanted sequences from high-throughput DNA sequencing data. Clear guides and examples.
Strand NGS offers powerful tools for analyzing next generation sequencing data, supporting DNA, RNA, ChIP, and methylation workflows for researchers.
Bujnicki lab shares resources, databases, and tools for research on nucleic acids and proteins, focusing on DNA/RNA structure, repair, and interactions.
Find clear, up-to-date documentation for ANNOVAR, a software tool used to annotate genetic variants across human and other genomes.
PRINSEQ helps you quickly clean and check DNA sequence data for bioinformatics and metagenomics research. Simple tools for quality control and preprocessing.