dbass.soton.ac.uk
DBASS5 - Aberrant Splice Database
http://dbass.soton.ac.uk/DBASS5
University of Southampton - Faculty of Medicine - dbass. DBASS5 is a publicly accessible resource containing details of aberrant 5' splice sites generated as a result in disease-causing mutations in human genes. DBASS5 is regularly updated and is intended as a reference tool for clinical geneticists, biochemists, cell biologists and all investigators studying consequences of genetic changes at the level of pre-mRNA splicing as well as mechanisms underlying 5' splice site selection.
dbass.soton.ac.uk
DBASS3 - Aberrant Splice Database
http://dbass.soton.ac.uk/DBASS3
University of Southampton - Faculty of Medicine - dbass. DBASS3 is a publicly accessible resource containing details of aberrant 3' splice sites generated as a result in disease-causing mutations in human genes. DBASS3 is regularly updated and is intended as a reference tool for clinical geneticists, biochemists, cell biologists and all investigators studying consequences of genetic changes at the level of pre-mRNA splicing as well as mechanisms underlying 3' splice site selection.
dbass.org.uk
DBASS5 - Aberrant Splice Database
http://www.dbass.org.uk/DBASS5
University of Southampton - Faculty of Medicine - dbass. DBASS5 is a publicly accessible resource containing details of aberrant 5' splice sites generated as a result in disease-causing mutations in human genes. DBASS5 is regularly updated and is intended as a reference tool for clinical geneticists, biochemists, cell biologists and all investigators studying consequences of genetic changes at the level of pre-mRNA splicing as well as mechanisms underlying 5' splice site selection.
dbass.org.uk
DBASS3 - Aberrant Splice Database
http://www.dbass.org.uk/DBASS3
University of Southampton - Faculty of Medicine - dbass. DBASS3 is a publicly accessible resource containing details of aberrant 3' splice sites generated as a result in disease-causing mutations in human genes. DBASS3 is regularly updated and is intended as a reference tool for clinical geneticists, biochemists, cell biologists and all investigators studying consequences of genetic changes at the level of pre-mRNA splicing as well as mechanisms underlying 3' splice site selection.
als-research.mit.edu
Genome Annotation (GENOA) file Server
http://als-research.mit.edu/genoa/index.html
This is the GENOA file server at MIT, providing access to genome alignments that detect loci and pertinent alternative transcript structures of genes in genomic sequences for the human genome. Related publications and online supplementary material. D Holste, C.B. Burge, et al. The making of mRNAs: computationally dissecting the alternative splicing of precursors by using the Hollywood database. In preparation. World-wide web Supplementary material. Genome Annotation (GENOA) pipeline. Aligns spliced cDNA ...
genes.mit.edu
Genome Annotation (GENOA) file Server
http://genes.mit.edu/genoa/index.html
This is the GENOA file server at MIT, providing access to genome alignments that detect loci and pertinent alternative transcript structures of genes in genomic sequences for the human genome. Related publications and online supplementary material. D Holste, C.B. Burge, et al. The making of mRNAs: computationally dissecting the alternative splicing of precursors by using the Hollywood database. In preparation. World-wide web Supplementary material. Genome Annotation (GENOA) pipeline. Aligns spliced cDNA ...
argonaute.mit.edu
Genome Annotation (GENOA) file Server
http://argonaute.mit.edu/genoa/index.html
This is the GENOA file server at MIT, providing access to genome alignments that detect loci and pertinent alternative transcript structures of genes in genomic sequences for the human genome. Related publications and online supplementary material. D Holste, C.B. Burge, et al. The making of mRNAs: computationally dissecting the alternative splicing of precursors by using the Hollywood database. In preparation. World-wide web Supplementary material. Genome Annotation (GENOA) pipeline. Aligns spliced cDNA ...