Open FenghuJi opened 4 years ago
MicrobiotaProcess
provides build_tree
function to build tree, this function is developed based on DECIPHER
(alignment) and phangorn
(phyDat, dist.ml, NJ, pml, optim.pml) packages. The input can be the fasta file (nucleotide sequence). You can provide your represent sequences. Or you can use other tools such as muscle, etc to build the tree, then use treeio
to make a phylo class tree.
Thanks a lot. But it seems that the phylo class genrated from both build_tree()
and treeio read.newick
doesn't work.
When I print the phylo tree, the consolo outputs
> tree
Phylogenetic tree with 2295 tips and 2293 internal nodes.
Tip labels:
2f4a2b08eec8d8d5f66dc0d20552881f, cc1f106dae404eca16e3b7d588d58645, 135ea3e4d147e2cf6e381bd218ca38c2, eb3357232ee140b5bd5de0c3babd10ca, 9b44baa49a601fb4b6c50c312c901778, 5881bb20a5699e35017633aa882befb5, ...
Unrooted; includes branch lengths.
and when I use the get_pcoa()
function, it outputs
> pcoares <- get_pcoa(obj=ps_qiime2,tree=tree_rooted,distmethod="unifrac", method="hellinger",tree=tree)
Error in get_dist.phyloseq(obj, distmethod = distmethod, ...) :
The tree should be required when the distmethod is `WeightUniFrac` or `UnWeightUniFrac`
The version of R is 4.0.0. Can you tell me what is the problem.
Ok, get_pcoa
is S3
method, when the obj
is phyloseq
class. The tree should be in the phyloseq
class. So you can use ps <- phyloseq(otu_table(ps_qiime2), sample_data(ps_qiime2),tax_table(ps_qiime2), yourtree)
, or ps <- phyloseq(otu_table(ps_qiime2), sample_data(ps_qiime2), tax_table(ps_qiime2), refseq(ps_qiime2))
if the represent sequences is in ps_qiime2
, to build the phyloseq
class.
Hello, when I use the
get_pcoa()
functionIt raised error:
But how can I get the phylo class tree? Could you please help me ? Thanks a lot.