About identifying unique sequences
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|
1
|
1990
|
April 24, 2014
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make.contigs() puts everything in scrap file
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|
1
|
2020
|
April 24, 2014
|
taxonomy outline
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0
|
7016
|
April 23, 2014
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Count following trim.seqs is way down
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4
|
4487
|
April 18, 2014
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screen.seqs problem
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5
|
4050
|
April 18, 2014
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difference between gg_13_5_99.gg.tax and gg_13_5_99.pds.tax
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|
1
|
2971
|
April 18, 2014
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Weighted Unifrac
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|
2
|
2010
|
April 17, 2014
|
Flip in trim.seqs
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|
8
|
6021
|
April 17, 2014
|
Output of rarefaction.single
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|
1
|
1729
|
April 15, 2014
|
Core genome
|
|
1
|
1715
|
April 15, 2014
|
sharedace for venn?
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|
1
|
2977
|
April 15, 2014
|
subsampling in MiSeq SOP
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|
3
|
4173
|
April 15, 2014
|
About alignment of R1&R2 details in make.contigs()
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|
1
|
2086
|
April 15, 2014
|
Is there such a thing as too much overlap?
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|
1
|
2785
|
April 15, 2014
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Old version of mothur
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|
7
|
16737
|
April 15, 2014
|
align.seqs_output file_ unique.flip.accnos
|
|
1
|
3176
|
April 15, 2014
|
Blast against PATRIC Pathogen Database?
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|
3
|
7352
|
April 15, 2014
|
Same barcode and sfffiles.txt does not work
|
|
2
|
3909
|
April 14, 2014
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equivalent of trim.flows for single-end Illumina reads
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|
2
|
2692
|
April 14, 2014
|
how to make group file
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|
1
|
2798
|
April 13, 2014
|
Sub-sampling is not admissible?
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|
0
|
6439
|
April 13, 2014
|
Removal of 2 barcodes and 2 primers using trim.seqs
|
|
4
|
3509
|
April 11, 2014
|
Orientation of mate-pairs for paired end illumina reads
|
|
4
|
4946
|
April 11, 2014
|
Summary taxonomy table from filtered .shared file
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|
3
|
4353
|
April 10, 2014
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how to generate a fasta file of all sequences in an otu?
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|
2
|
1987
|
April 10, 2014
|
hard start for screen.seqs
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|
1
|
3098
|
April 9, 2014
|
make.shared() doesn't recognize 'label=0.03' for MiSeq run
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|
3
|
4135
|
April 8, 2014
|
No stability.trim.contigs.fasta as output of make.contigs
|
|
5
|
3955
|
April 8, 2014
|
MOTHUR in the cloud
|
|
0
|
4747
|
April 8, 2014
|
Primer.design
|
|
3
|
2861
|
April 4, 2014
|