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Readseq 2.1.30 (
doc
)
1. Overview
2. Data & Settings
3. Results
Upload your sequence file:
Or paste your sequence(s) here:
(
load an example of alignment
)
Settings
Input format:
Auto-detect
IG/Stanford
GenBank/GB
NBRF
EMBL
GCG
DNAStrider
Pearson/Fasta
Phylip3.2
Phylip
Plain/Raw
PIR/CODATA
MSF
PAUP/NEXUS
XML
Blast
SCF
Clustal
FlatFeat/FFF
GFF
ACEDB
Output format:
IG/Stanford
GenBank/GB
NBRF
EMBL
GCG
DNAStrider
Pearson/Fasta
Phylip3.2
Phylip
Plain/Raw
PIR/CODATA
MSF
PAUP/NEXUS
Pretty
XML
Clustal
FlatFeat/FFF
GFF
ACEDB
Advanced Settings...
Remove gaps