DBASS3 and DBASS5 provide comprehensive repositories of new exon boundaries that were induced by pathogenic mutations in human disease genes. Aberrant 5?- and 3?-splice sites were activated either by mutations in the consensus sequences of natural exon–intron junctions (cryptic sites) or elsewhere (‘de novo’ sites). DBASS3 and DBASS5 currently contain approximately 900 records of cryptic and de novo 3?- and 5?-splice sites that were produced by over a thousand different mutations in approximately 360 genes. DBASS3 and DBASS5 data can be searched by disease phenotype, gene, mutation, location of aberrant splice sites in introns and exons and their distance from authentic counterparts, by bibliographic references and by the splice-site streng...
A set of 43 337 splice junction pairs was extracted from mammalian GenBank annotated genes. Expresse...
Representative set of mutations which significantly alter splicing in all evidence types analyzed by...
Cryptic splice sites are used only when use of a natural splice site is disrupted by mutation. To de...
Despite a growing number of splicing mutations found in hereditary diseases, utilization of aberrant...
Despite a growing number of splicing mutations found in hereditary diseases, utilization of aberrant...
The frequency distribution of mutation-induced aberrant 3' splice sites (3'ss) in exons and introns ...
We compiled sequences of previously published aberrant 3' splice sites (3'ss) that were generated by...
Background: The three consensus elements at the 3' end of human introns-the branch point sequence, t...
To determine the impact of the intron-exon architecture and splice site strength on splice site sele...
Deep sequencing has shown that over 90% of human genes undergo alternative splicing. The splicing pr...
Ensus value (CV) method. Donor and acceptor sites are considered separately. The vertical dashed lin...
A total of 101 different examples of point mutations, which lie in the vicinity of mRNA splice junct...
Auxiliary splicing signals play a major role in the regulation of constitutive and alternative pre-m...
RNA splicing is an important aspect of gene regulation in many organisms. Splicing of RNA is regulat...
A database (SpliceDB) of known mammalian splice site sequences has been developed. We extracted 43 3...
A set of 43 337 splice junction pairs was extracted from mammalian GenBank annotated genes. Expresse...
Representative set of mutations which significantly alter splicing in all evidence types analyzed by...
Cryptic splice sites are used only when use of a natural splice site is disrupted by mutation. To de...
Despite a growing number of splicing mutations found in hereditary diseases, utilization of aberrant...
Despite a growing number of splicing mutations found in hereditary diseases, utilization of aberrant...
The frequency distribution of mutation-induced aberrant 3' splice sites (3'ss) in exons and introns ...
We compiled sequences of previously published aberrant 3' splice sites (3'ss) that were generated by...
Background: The three consensus elements at the 3' end of human introns-the branch point sequence, t...
To determine the impact of the intron-exon architecture and splice site strength on splice site sele...
Deep sequencing has shown that over 90% of human genes undergo alternative splicing. The splicing pr...
Ensus value (CV) method. Donor and acceptor sites are considered separately. The vertical dashed lin...
A total of 101 different examples of point mutations, which lie in the vicinity of mRNA splice junct...
Auxiliary splicing signals play a major role in the regulation of constitutive and alternative pre-m...
RNA splicing is an important aspect of gene regulation in many organisms. Splicing of RNA is regulat...
A database (SpliceDB) of known mammalian splice site sequences has been developed. We extracted 43 3...
A set of 43 337 splice junction pairs was extracted from mammalian GenBank annotated genes. Expresse...
Representative set of mutations which significantly alter splicing in all evidence types analyzed by...
Cryptic splice sites are used only when use of a natural splice site is disrupted by mutation. To de...