HPVomics

A therapeutic and epitome resource for Human Papillomaviruses

  • HPVomics Overview
    • HPVomics provides a unique blend of potential therapeutic knowledge, HPV epitome, interactive genomic annotation browser and genomic analysis.

    • HPVomics is classified in different sections represent individual components mainly therapeutics (i.e. siRNAs, sgRNAs, antiviral peptides etc.), vaccine epitopes (IEDB epitopes, MHC-I and -II binders, B-cell, CTL epitopes), genomes, genome browser, epitope map and tools.

    • It also provide HPV epitome prediction algorithm "HPVepi" to predict the B-cell and T-cell (MHC-I and II) epitopes.

    • Detail organization
  • HPV Browser
    • To navigate through the HPV genomes, we set up a "HPVomics genome browser" which facilitates graphical visualization of annotations.

    • Various tracks includes HPV reference genome, Genes, CDS, mRNA, exon, CpG islands, promoter, TATA box, CAAT signal, 5` UTR, repeat region, protein binding site, polyA signal sequence, and secondary structure information

    • The upper panel shows the positional scale (ruler) to navigate through genomes along with HPV reference sequence. Distinct annotation features were shown in separate color blocks.

  • HPVepi
    • This is an algorithm for the prediction of HPV B-cell and T-cell (MHC-I/II) epitopes

    • User can paste or upload peptide sequence to known the potentially of peptides to become epitopes

  • Epitope Map
    • This is an interactive map of epitopes. In Epitope map, data is classified according the viral proteins with priority given to the HPV oncoproteins (E6, E7, E5).

    • It contains information such as IEDB id, start and end coordinates with gene region, epitope length, epitope sequence, and HLA allele type. Epitopes are mapped on the reference viral protein sequences.

  • HPV BLAST
    • HPVblast:: To find similarity and align query sequence to the HPV genomes and genes.




  • ConBlock
    • This tool allows user to select highly aligned regions of a DNA and protein multiple sequence alignment which can be used and more suitable for phylogenetic analysis.