Bioinformatics Asked on December 11, 2021
I wish to convert a kraken2 or metaphlan2 report into the R package to analyze using Phyloseq.
I have performed obtained an importation and Phyloseq analysis, but the result was not correct.
library("phyloseq")
library("biomformat")
otu_Rat11 <- read_biom("Rat11.biom")
otumat_Rat11 = as(biom_data(otu_Rat11), "matrix")
OTU_Rat11 <- otu_table(otumat_Rat11, taxa_are_rows=TRUE)
str(OTU_Rat11)
#Formal class 'otu_table' [package "phyloseq"] with 2
#slots ..@ .Data : num [1:1018, 1] 942 433 3007 116765 15103 ... .. ..-
#attr(*, "dimnames")=List of 2 .. .. ..:?ℎ?[1:1018]"186826""33958""1578"
#"33959".........:chr[1:1018] "186826" "33958" "1578" "33959"......... :
# chr "sa1" ..@ taxa_are_rows: logi TRUE
taxmat_Rat11 = as.matrix(observation_metadata(otu_Rat11), rownames.force=TRUE)
TAX_Rat11 = tax_table(taxmat_Rat11)
physeq_Rat11 = phyloseq(OTU_Rat11, TAX_Rat11)
str(physeq_Rat11)
#Formal class 'phyloseq' [package "phyloseq"] with 5 slots ..@ otu_table:Formal
#class 'otu_table' [package "phyloseq"] with 2 slots .. .. ..@ .Data : num
#[1:1018, 1] 942 433 3007 116765 15103 ... .. .. .. ..- attr(*, "dimnames")=List
# of 2 .. .. .. .. ..:?ℎ?[1:1018]"186826""33958""1578""33959".............: chr
#[1:7] "taxonomy1" "taxonomy2" "taxonomy3" "taxonomy4" ... ..@ sam_data : NULL ..
#@ phy_tree : NULL ..@ refseq : NULL –
Now I try to obtain @ sam_data
sampledata = sample_data(otu_Rat11)
#Error in access(object, "sam_data", errorIfNULL) : sam_data slot is empty.
What do with sample data and how to merge several phyloseq-format datasets from different metagenomes?
Get help from others!
Recent Answers
Recent Questions
© 2024 TransWikia.com. All rights reserved. Sites we Love: PCI Database, UKBizDB, Menu Kuliner, Sharing RPP