Consensus

Functions
Home

Browse
Export
Slice
Consensus
Compare
Search
Probe
Align
Trim
Download
Curate
More Tools...

About
Citation
Tutorial
FAQ
Objectives
Methods
Contact

My Interest List
0 sequences

remove all
collapse all
show marked

My Taxonomy

Changing taxonomy will empty My Interest List.
 
Trim a batch of sequences using corresponding quality scores
Use this tool to trim your fasta sequences according to their quality scores. A fasta file of your trimed sequences will be sent by email along with a spreadsheet of results. This is a beta tool, so please provide feedback. The program is based on the work of David Ow.
My fasta formatted sequence file:
My fasta formatted quality file:

Options:

Good quality threshold:
Set the quality score required for a base call to be considered as confident.



Window size:
Set the size of the span to be considered collectively.



Percentage:
Set the percentage of bases that must surpass the threshold for the window to be considered good quality.


Bases returned upper-case.
Bases returned as upper-case, sub-threshold quality positions are converted to lower-case.
Bases returned as upper-case, sub-threshold quality positions are converted to N.


Email address to send results (required):


Trim now.
 
  • Last Database Update: June 16, 2008 1:58PM
  • 232812 aligned 16S rDNA records >1250nt