Please read an important announcement about the future of the HCV database here.

SeqPublish: Sequence Alignment Publishing Tool

Purpose: This interface takes a sequence alignment (nucleotides or amino acids) and replaces residues identical to a reference sequence with dashes. The reference sequence is either the first sequence in the alignment, or Seqpublish can create a consensus sequence and use that. You can download your alignment, including the consensus sequence, to use in analyses.

Input

Paste your input here [SAMPLE INPUT]
or upload your file

Options

Desired line length	characters
Insert a space every	columns
Select output format

Consensus

Check to create a consensus for your alignment and fill out the information below
Unanimity threshold	("Unanimous" consensus symbols are shown as capital letters.)
Majority threshold	("Majority" symbols are shown as lowercase letters. When no majority occurs, a "?" appears.)
Ignore trailing blanks	(If your sequences have different lengths, the ends of shorter sequences will be padded with blanks. When this box is checked, these blanks will be ignored when creating the consensus.)

Questions or comments? Contact us at hcv-info@lanl.gov