Mapping of DNA sequence fragments in FASTA format:
* entries are required
* It's better to do short fragments (<10 Kb) mapping
1. *Please copy & paste in the fragments data in proper FASTA format:
or upload data file
2. Please give the target genomic DNA sequence data file (one sequence in FASTA format.):
*
3. * Please give the description of the un-annotated target genomic DNA sequence, or Genbank data file or Genbank header file (.gbheader produced by previous DNannotator run).
You may check this box if this is your first time to run annotation for this sequence on DNannotator. Then, please fill in the following information but no Genbank file will be needed. A Genbank header file will be created for you based on data from FASTA sequence and the information you provided here.
Sequence description: Chromosome: 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 X Y
Un-annotated Genbank file (should be the one generated by DNannotator in previous analysis for the same target sequence):
4. Adjustable parameters.
Annotation fashion: BLAT-based BLAST-based
Additional parameters for BLAT-based annotation:
Additional parameters for BLAST-based annotation:
For annotation,
First filter
@ Minimum size of match for valid hits bp (If your fragment sequence is shorter, please decrease this number accordingly) @ Minimum percentage of identities for valid hits 95% 96% 97% 98% 99% 100% @ The maximum length difference between query sequence and matching fragment is bp
@ Minimum size of match for valid hits bp (If your fragment sequence is shorter, please decrease this number accordingly)
@ Minimum percentage of identities for valid hits 95% 96% 97% 98% 99% 100%
@ The maximum length difference between query sequence and matching fragment is bp
Second filter
@ Only the best matches will be used for annotation All hits above filter will be used for annotation
5. Choice of outputs:
Show BLAST/BLAT annotation evidence of match identity percentage in Genbank annotation and features table
Annotation Genbank format data or Genbank format features (gbheader)
viewable in Vector NTI or Artemis
Feature table ready for database in tab-delimited format
Features failed to be annotated
Duplicated features (possibly false positive due to homologs)
Original BLAST/BLAT output
Annotation evidence (compact parsed BLAST/BLAT data)
Original full-length Genbank format data (with sequence body)
Original gbheader
6. Please specify the email address to which the outputs will be delivered:
Email address *
choice of output in gzip compressed format: yes, zip it no, original data please
Your email box accepts message size limit of 1 MB 2 MB 4 MB 6 MB per message
If your input data file is from a Mac machine, please be sure to check this box
BLAT created by Jim Kent, 2002 is used