ReAlignerV

ReAlignerV is an alignment tool focusing on genomic nucleotide
sequences upstream of genes. ReAlignerV integrates TRANSFAC(R) Match(TM)
results to detect the conserved TFBSs.
ReAlignerV is robust against transposable element insertions.

Project Activity

See All Activity >

License

GNU General Public License version 2.0 (GPLv2)

Follow ReAlignerV

ReAlignerV Web Site

Other Useful Business Software

Our Free Plans just got better! | Auth0

With up to 25k MAUs and unlimited Okta connections, our Free Plan lets you focus on what you do best—building great apps.

You asked, we delivered! Auth0 is excited to expand our Free and Paid plans to include more options so you can focus on building, deploying, and scaling applications without having to worry about your security. Auth0 now, thank yourself later.

Try free now

Rate This Project

User Reviews

Be the first to post a review of ReAlignerV!

Additional Project Details

Intended Audience

Quality Engineers

Programming Language

Perl

Database Environment

Flat-file

Related Categories

Perl Bio-Informatics Software

Registered

2009-04-07

Similar Business Software

Evo 2

Evo 2 is a genomic foundation model capable of generalist prediction and design tasks across DNA, RNA, and proteins. It utilizes a frontier deep learning architecture to model biological sequences at single-nucleotide resolution, achieving near-linear scaling of compute and memory relative to...

See Software
Evo Designer

Evo Designer is an advanced tool developed by the Arc Institute, leveraging the capabilities of the Evo 2 genomic foundation model to facilitate DNA sequence generation and analysis. This platform enables users to input nucleotide sequences or specify organisms, prompting the model to generate...

See Software
Geneyx

Geneyx Analysis is a comprehensive solution for next-generation sequencing (NGS) data that can scale the process of FASTQ to clinical reports for hospital and commercial labs. This advanced platform integrates machine learning and AI-based features to identify novel biomedical insights, while...

See Software