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PipMaker computes alignments of similar regions in two DNA sequences. The resulting alignments are summarized with a ``percent identity plot'', or ``pip'' for short. MultiPipMaker allows the user to see relationships among more than two sequences. All pairwise alignments with the first sequence are computed and then returned as interleaved pips. Moreover, MultiPipMaker can be requested to compute a true multiple alignment of the input sequences and return a nucleotide-level view of the results. Registration not required.
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VISualization Tools for Alignments: VISTA is a comprehensive suite of programs and databases for comparative analysis of genomic sequences. Registration not required.
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While standard alignment methods rely on comparing single residues and imposing gap penalties, DIALIGN constructs pairwise and multiple alignments by comparing entire segments of the sequences. No gap penalty is used. This approach can be used for both global and local alignment, but it is particularly successful in situations where sequences share only local homologies. Registration not required.
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Compare gene order between two small bacterial genomes Registration not required.
Click here for more informationsCompute post test probability, Multiple comparisons correction Registration not required.
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DNA or genome alignment and visualization tool based on blastz alignment program. Alignments can be automatically submitted to rVista 2.0 to identify evolutionary conserved transcription factor binding sites. Registration not required.
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This online program helps to evaluate the quantity of primers and nucleotides for optimal PCR reaction and the necessary number of cycles. Registration not required.
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The HUGO Gene Nomenclature Committee (HGNC) has assigned unique gene symbols and names to over 33,000 human loci, of which around 19,000 are protein coding. http://genenames.org is a curated online repository of HGNC-approved gene nomenclature and associated resources including links to genomic, proteomic and phenotypic information, as well as dedicated gene family pages. Registration not required.
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FOLDALIGN is an algorithm for local or global simultaneous folding and aligning two or more RNA sequences and is based on the Sankoffs algorithm (SIAM J. Appl. Math., 45:810-825, 1985). Foldalign can make pairwise local or global alignments and structure predictions. FoldalignM makes a multiple global alignment and structure prediction. Registration not required.
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With more than 900,000 human-edited definitions, Acronym Finder is a largest dictionary of acronyms, abbreviations, and initialisms. Combined with the Acronym Attic, Acronym Finder contains more than 4 million acronyms and abbreviations. Registration not required.
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Click here for more informationsOverlapping Primers creates multiple overlapping PCR products in one sequence. Registration not required.
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Click here for more informationsDistributions: Binomial, Normal, Student's T, Chi Square, Fisher's F Registration not required.
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Category: Gene information search, Gene expression
WashU Human Epigenome Browser allows: Epigenome
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