BioSAVE is a software tool that enables the visualization and annotation of biological sequences. It helps users analyze, annotate, and interpret sequence data, allowing for efficient and accurate sequence annotation. The software is designed for researchers, bioinformaticians, and biologists to improve their data analysis workflow.
BioSAVE is a handy software application specially designed for visualizing and analyzing DNA or protein sequences, along with their annotations expressed in GFF format. It is a versatile tool that offers users the ability to manipulate and customize annotations according to their needs.
Initially developed by Richard Pollock and Boris Adryan, BioSAVE was created primarily to visualize predicted transcription factor binding sites efficiently, but its capabilities have grown throughout the years. Today, it supports additional helpful "tracks" of data, such as sequence conservation or ChIP enrichment data alongside predicted motifs, among others.
BioSAVE is an excellent tool for researchers conducting genomic studies and requires a healthy amount of RAM and a fast processor (G5 or Intel) to handle larger datasets of over 3 Mb.
Overall, BioSAVE is an extremely efficient and useful software that has helped researchers in advancing their genomic studies, providing a user-friendly interface complete with customizable options, making it a valuable asset to the field.
Initially developed by Richard Pollock and Boris Adryan, BioSAVE was created primarily to visualize predicted transcription factor binding sites efficiently, but its capabilities have grown throughout the years. Today, it supports additional helpful "tracks" of data, such as sequence conservation or ChIP enrichment data alongside predicted motifs, among others.
BioSAVE is an excellent tool for researchers conducting genomic studies and requires a healthy amount of RAM and a fast processor (G5 or Intel) to handle larger datasets of over 3 Mb.
Overall, BioSAVE is an extremely efficient and useful software that has helped researchers in advancing their genomic studies, providing a user-friendly interface complete with customizable options, making it a valuable asset to the field.
What's New
Version 0.11: N/A