A Bio2BEL package for converting InterPro to BEL
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Updated
Apr 15, 2019 - Python
A Bio2BEL package for converting InterPro to BEL
UniParc dataset describing ~300 million protein sequences converted into relational tables accessible through Google BigQuery (and as Parquet files).
Mapping domain co-occurrence networks with emphasis on c-d-GMP binding domains.
Brivez is a bioinformatic tool thought as Quality of Life's improvement, providing high quantity of data in a snap, giving you a quick view on what you could find inside your transcriptome/sequences' list.
👐 TADOSS: TAndem DOmain Swap Stability predictor
Using BLAST and Transdecoder.
An R package to identify plant transcription factors from protein sequence data and classify them in families
THIS PROJECT IS NO LONGER SUPPORTED See Brivez Instead!! https://github.com/furacca/brivez/ - ------------------------------------------ - Cuterle is a bioinformatic tool which return an output file containing every domain annotated by InterProScan via Pfam or SMART analysis from the list of protein submitted.
CroMaSt (Cross Mapper of domain Structural instances) is an automated iterative workflow to clarify domain definition by cross-mapping of domain structural instances between domain databases.
dom2vec: Protein domain embeddings
Pipeline to generate a profile-HMM of Kunitz domain starting from the structure of BPTI.
Snakemake pipeline for searching genomic sequences for those encoding proteins containing domains of choice
Automated analysis tool for mutations in promoters, transcription factor binding sites, coding regions and protein domains in the context of gene regulatory networks.
Refining Domain Boundaries and Performing Large Scale Parsing
Comparison of protein learning
FAS - Tool for Feature Architecture Similarity calculation
MetaDome is aimed at professionals in the (bio-)medical field of human genetics who wish to visualize the position of their mutation of interest in the context of general population-based genetic variation and provide detailed information of pathogenic variants found across homologous domain positions.
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