Hi,
Sorry in advance, i’m a novice with mothur…I encounter some problems with the filter.seqs command
I have run the screen.seqs command and obtained :
summary.seqs(fasta=all.trim.unique.good.align)
Using 1 processors.
Start End NBases Ambigs Polymer NumSeqs
Minimum: 1045 5331 195 0 3 1
2.5%-tile: 1046 5339 224 0 3 1312
25%-tile: 1046 5459 253 0 4 13112
Median: 1046 5711 262 0 5 26224
75%-tile: 1046 6098 269 0 5 39336
97.5%-tile: 1046 6324 282 0 6 51136
Maximum: 1046 6428 314 0 8 52447
Mean: 1045.99 5770.99 259.602 0 4.72832
of Seqs: 52447
Output File Names:
all.trim.unique.good.summary
Then I run the filter.seqs command, and seems like all the columns have been removed...
filter.seqs(fasta=all.trim.unique.good.align-silva.gold.align, trump=., vertical=T, processors=2)
Using 2 processors.
Creating Filter…
Running Filter...
Length of filtered alignment: 0 Number of columns removed: 50000 Length of the original alignment: 50000 Number of sequences used to construct filter: 57628
Output File Names:
allsilva.filter
all.trim.unique.good.filter.fasta
silva.gold.filter.fasta
mothur > summary.seqs(fasta=all.trim.unique.good.filter.fasta)
Using 2 processors.
Start End NBases Ambigs Polymer NumSeqs
Minimum: -1 -1 0 0 1 1
2.5%-tile: 0 0 0 0 1 1312
25%-tile: 0 0 0 0 1 13112
Median: 0 0 0 0 1 26224
75%-tile: 0 0 0 0 1 39336
97.5%-tile: 0 0 0 0 1 51136
Maximum: -1 -1 0 0 1 52447
Mean: 0 0 0 0 1
of Seqs: 52447
Output File Names:
all.trim.unique.good.filter.summary
Any help?