Site search
search our web site using the search box (top right of the page, below the virus)
Sequence search
search for sequences by selecting from numerous criteria
Advanced search
create your own search interface, access to all database info
Geography search
retrieves HCV sequences based on geographical distribution
CTL epitopes
search for CTL epitopes by protein, immunogen, HLA, author, keywords
T helper epitopes
search for T helper epitopes by protein, immunogen, HLA, author, keywords
Antibodies
search for HCV antibodies by protein, immunogen, AB type, isotype, author, keywords
Translate
nucleotide sequences to 1-letter amino acids
Gapstreeze
Remove columns with more than a given % of gaps
Consensus
compute a customizable consensus
Gene Cutter
clip genes from a nucleotide alignment, codon-align and translate
HCValign
aligns your sequence(s) using either the multiple alignment program MAFFT, or using the appropriate hidden Markov model.
SynchAligns
align overlapping alignments to one another
Primalign
align a nucleotide sequence (e.g., primer) to the complete genome alignment
Epilign
align a protein sequence (e.g., epitope) to the appropriate protein alignment
Pixel
This tool generates a PNG image of an alignment using 1 or more colored pixel(s) for each residue.
PepMap
This tool can be used to map epitopes, functional domains, or any protein region of interest.
Genotypes
Old and new HCV genotypes in the database
Geography
geographic distribution of HCV database sequences
Alignments
Curated sequence and reference alignments for all genes
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Sequence locator
find the standard numbering of your nucleotide or protein sequence in H77
HCV BLAST
find sequences similar to yours in the HCV database
VESPA
detect signatures: residues with different frequencies in two sequence sets
PCOORD
multidimensional analysis of sequence variation
N-Glycosite
find potential N-linked glycosylation sites in a protein alignment
SNAP
calculate synonymous/non-synonymous substitution rates
Highlighter
matches, mismatches, transition and transversion mutations, and silent and non-silent mutations in an aligned set of nucleotide sequences.
TreeMaker
generate a quick-and-dirty phylogenetic tree
Search interface tree builder
create a tree from sequences returned from database search
FindModel
find which evolutionary model best fits your sequences
Branchlength
calculates branch lengths between internal and end nodes based on a Newick treefile
Format Converter
converts between 18 standard sequence formats
SeqPublish
to make publication-ready alignments
Protein Feature Accent
provides an interactive 3-D graphic of selected HCV proteins;
the user can map a sequence feature and see where it occurs spatially.
PeptGen
generate overlapping peptides from a protein sequence
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