Frequently asked questions
1. May I use the figures from
your website in my publications, presentations or
website etc?
2. How can I know the update
time/status of your database?
3. I found some VF (or other
important information) missed in your database, what
can I do?
4. Would you please send me the
virulence factors data set of VFDB?
5. Where can I get a copy of
all protein/DNA sequences from VFDB for local BLAST?
6. Why the new comparison tables
cover additional VFs/genes? (Some VFs listed in the
comparison tables offer links to related literatures
in PubMed instead of detail description pages in VFDB,
why?)
7. Oh, I found all/some plasmids
from the genome of xxx were missed from your comparison
table.
8. Why some released/published
genomes were not included into your comparison table?
9. May I send you the entire
pathogenomic table of my newly determined genome?
How to do?
Q1: May I use the figures from your
website in my publications, presentations or website
etc?
A: All
figures here can be used for non-profit purpose freely
as long as you refer VFDB as origin or cite our publication.
Commercial users should contact
us for detail information. Note that some figures
were reproduced from other literatures (citation information
should present above the individual figures).
Q2: How can I know the update time/status
of your database?
A: The
last update time of VFDB is displayed at the bottom
right of the main page.
You can find the most up-to-date statistic information
(summary and detailed tables) about VFDB in the status
page. For current status of comparative results,
you can visit the
part of comparative pathogenomics of status page.
Q3: I found some VF (or other important
information) missed in your database, what can I do?
A: Researchers
are kindly invited and encouraged to deposit their
new results about VFs at VFDB. Submission might either
be performed through the feedback
form or by email to .
Q4: Would you please send me the
virulence factors data set of VFDB?
A: We
would always like to help users for academic research
purpose. However, please note that the information
in VFDB is not just a simple table that can be easily
viewed in local tools such Excel. Actually it contains
several independent tables with many cross-links.
So we believe that the best way to view the content
of VFDB is to access it via the CGI scripts we provided
by your browser instead of download a local version.
Of course, we can provide users a local version of
our data, or any portion of it for local use, if you
insist. But you'd better let us know what kinds of
information you want. So we may prepare a special
dataset (maybe a table) for you. Otherwise, it may
puzzle you if we just send the dump of our database
to you. Users can contact us through the feedback
form or by email to .
NOTE: a simplified copy of all
virulence factors with related descriptions is monthly
released in Excel format from the download
page now.
Q5: Where can I get a copy of all
protein/DNA sequences from VFDB for local BLAST?
A: We
encourage users to use the web-blast
service of VFDB to query by their own sequences
since it offers direct links to individual genes pages
in the result. However, the sequences in FASTA format
are monthly released for local use from the download
page if you need to process large amount of queries.
Q6: Why the new comparison tables
cover additional VFs/genes? (Some VFs listed in the
comparison tables offer links to related literatures
in PubMed instead of detail description pages in VFDB,
why?)
A: The
previous release of VFDB covers only experimentally
demonstrated VFs, however, by introducing the comparative
genomics approaches the current release try to also
include those genome predicted VFs for comparative
analysis. That's one of the reasons of the additional
VFs listed in the comparison table. Another reason
is that the previous release usually chooses one representative
pathvar/serotype of each genus for collection of VFs.
Since genomes of various pathogens are available,
some additional VFs need to be listed in the table
for genome comparison. Anyway, we are updating the
content to try to provide full information for all
VFs ASAP.
Q7: Oh, I found all/some plasmids
from the genome of xxx were missed from your comparison
table.
A: Bacteria
usually carry a set of plasmids, most of which are
irrelated to virulence. Therefore, currently we include
only those virulence-related plasmids in VFDB (i.e.,
those encode known or potential VF genes).
Q8: Why some released/published genomes
were not included into your comparison table?
A: In
general, we intend to include all publicly available
genomes into the comparison table timely. Reasons
for the missing genomes could be:
1) For convenience of later data storage and process,
only genomes that are available from NCBI's
RefSeq database can be analyzed by the current
pipeline for comparison (both pathogenic and non-pathogenic
isolates). We are sorry for those genomes only released
from authors' own website or for any reason not be
included in RefSeq.
2) The comparison tables are scheduled monthly
update by monitoring information from the Complete
Microbial Genomes webpage of NCBI. So newly released
genomes will be included within a month. Please contact
us if you have any urgent request.
3) Currently, we have difficulty to analyze a few
of unpublished genomes of less documented species/subspecies
or non-clinical isolates. We will include them once
the relevant publications or sufficient background
information are available. We will highly appreciate
if the authors can send us the pathogenomic table
of their new genomes (see
Q9 for instruction).
Q9: May I send you the entire pathogenomic
table of my newly determined genome? How to do?
A: Researchers
are kindly invited and encouraged to send us the known
or analyzed pathogenomic data of their new genomes.
Please follow the steps bellow:
1) Go to the full comparison page of pathogenomic
composition of the pathogen you are going to submit
(click the genus of your pathogen in left menu, for
example Listeria,
and then click the underlined 'Comparative pathogenomics'
link in the page).
2) Scroll down to the bottom of the page, click the
download icon ( )
and save the current table into Excel format.
3) Edit the Excel table, add column(s) for the new
genome(s) and fill the cells with corresponding systematic
ID (i.e. locus_tag in GenBank file) of the homolog
if the VF genes present in the genome, or leave it
blank if absent.
4) Save the table and send it to .
We will validate your table content before load it
to the database, and will contact the author if any
conflicts found.
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