Gene structure, introns and exons, splice sites
Predict genes by comparing genomic sequences from evolutionary related organisms to each other.
Find information about the roles that alternative splicing variants play in protein structure and function.
Access and mine enormous alternative splicing information.
Search for alternative splice events and the resultant isoform splice patterns of genes from human, and other model species.
Search for alternatively spliced genes.
Generate graphs for gene alternative slicing.
Search for comprehensive information on splicing by exon skipping in human genome.
Detect exon-intron structure of a gene by comparing the genomic sequence to the related ESTs.
Find information about alternative splicing gene variants.
Carry out simulated RT-PCR to detect transcript variants.
Find gene models including alternative splicing events from genomic alignment of mRNA, EST and protein sequences.
Analyze alternative splicing events in custom gene datasets.
Predict gene in eukaryotic genomic sequences based on a generalized hidden Markov model.
Derive Transcript Patterns from AltSplice Splice Patterns and search for information on polyA sites.
Search for information about the spliceosomal introns of the yeast Saccharomyces cerevisiae.
Search for comprehensive information about alternatively spliced genes of mammals.
Find information related to alternative splicing (AS) events.
Find information about aberrant splice sites.
Use a collection of methods to analyze and graphically represent various DNA parameters.
Search for alternative splice forms (ASforms) from nine eukaryotic organisms; calculate of the tissue-NAEs, tissue-NCEs and tissue-NSS in human genome.
Search for annotated information about gene structure, function and expression, and alternative splicing events.
Search for EST-derived alternative splicing in human genome.
Rapidly analyze exon sequences to identify putative human exonic splicing enhancers (ESEs).
Search for information on the exon/intron structure of eukaryotic genes.
An algorithm designed to retrieve, compare and search for the exon-intron structure of existing gene annotations.
Identify exonic splicing silencers and predict if a coding SNP abolishes exonic splicing silencer motifs.
Asoftware tool for identifying and removing the vector from raw DNA sequence data without prior knowledge of the vector sequence.
Predict gene structures of plant genomes.
Find genes whose promoter regions have G-quadruplex motifs.
Search for annotated information on alternatively spliced human transcripts.
Search for annotated information on alternative gene splicing.
Search for Homo Sapiens Exon, Intron and Splice regions.
Search for putative alternative splicing information from human and mouse UniGene clusters.
A unified resource for analyzing effects of alternative splicing events in the context of protein structures.
Predict splicing phenotypes by identifying sequence changes that disrupt or alter predicted ESEs.
Search for known mammalian splice site sequences and other related information.
Search for occurrences of the four major alternative-splicing modes in human genome.
A web-based tool for splice-site analysis.
Search for information on alternative splice events at GYNGYN donors and NAGNAG acceptors.
Search and compare alternative splicing events in 15 animal species.
Explore the molecular biology and genomics of C. elegans with a special emphasis on alternative splicing.
Search for information on genome architecture and design in unicellular genomes.
Search for information on orthologous U12-introns from completely sequenced eukaryotic genomes.
Search for information on experimentally validated human noncoding fragments with gene enhancer activity as assessed in transgenic mice.
Search for information about all introns encoded in the nuclear and mitochondrial genomes of the yeast Saccharomyces cerevisiae.
Search for data from the Yeast Deletion, Mitochondrial Proteomics, and Yeast Expression Projects.
Deformation energy and nucleosome-positioning score calculator.
Search for computationally predicted human gene structure and splice variants derived from human mRNAs and ETS.