All functions
|
ERR260132
|
Precomputed lineage calling and coverage example. |
align_long_reads()
|
Align long reads (for instance from nanopore sequencing) to a reference
database. |
align_short_reads()
|
Aligns metagenomic shotgun reads against a reference. |
annotate_contigs()
|
Annotate diamond database hits with transcript info. |
annotate_silva()
|
Annotate the sequences in the SILVA database file. |
as.matrix(<mbquant>)
|
Convert a mbquant data table to a matrix. |
as_phyloseq()
|
Converts the denoise artifact to a phyloseq object. |
association()
|
Run differential association tests between taxa counts and exogenous
factors. |
build_lineage()
|
Build the lineage from a SILVA path string. |
combinatorial_association()
|
Run differential association tests between between all combinations of a
factor variable. Can be used as post-hoc test for regression. |
config_align()
|
Build a configuration for the alignment workflows. |
config_association()
|
Build a configuration for the alignment workflows. |
config_count()
|
Build a configuration for the transcript counting workflow. |
config_demultiplex()
|
Build a configuration for the demultiplexing workflow. |
config_denoise()
|
Build a configuration for the DADA2 workflow. |
config_layout()
|
Build a configuration for the plate layout. |
config_power()
|
Build a configuration for power analysis. |
config_preprocess()
|
Build a configuration for raw read preprocessing. |
config_reference()
|
Build a configuration for the reference removal workflow. |
config_rep()
|
Build a configuration for the rate workflow. |
config_slimm()
|
Build a configuration for the SLIMM workflow. |
config_sra()
|
Build a configuration for the SRA submission workflow. |
count_references()
|
Count alignment hits to a reference database. |
demultiplex()
|
Splits FASTQ files into individual samples. |
denoise()
|
Runs a full DADA2 workflow. |
discretize()
|
Discretize all continuous variables in a data frame. |
download_bacterial_transcripts()
|
Download the entire ENSEMBL transcript DB for bacteria. |
download_files()
|
Download a list of files. |
download_sra()
|
Download data from SRA. |
effective_lengths()
|
Calculate the effective transcript lengths. This is the mean number of
positions in the transcript the fragment could map to. |
em_count()
|
Count transcripts using an Expectation Maximization (EM) algorithm. |
filter_counts()
|
Filter low presence taxa from a count matrix. |
filter_reference()
|
Filter a set of reference sequences from the data set.seed |
find_read_files()
|
Find read files in a given directory. |
find_taxa()
|
Checks whether taxa from one taxonomy table are contained in another table. |
layout()
|
Generate a plate layout from a sample manifest. |
mbtools
|
mbtools. |
merge_transcripts()
|
Merge transcripts into a single database |
mock_plot()
|
Creates a plot of measured taxa quantifications vs. reference quantification. |
mockrobiota()
|
Downloads a complete data set from mockrobiota. |
mothur_to_dada()
|
Converts taxa annotations from mothur format to dada2 format. |
normalize()
|
Normalize a set of read counts across samples |
orlitsky()
|
Orlitsky's diminishing attenuation estimator (q2/3). |
parse_ensembl_id()
|
Parse annotations from an ENSEMBL id |
plot_counts()
|
Plots counts for several taxa across a co-variable |
plot_entropy()
|
Plots the distribution of base entropy for each cycle. |
plot_lengths()
|
Plots the distribution of sequence lengths with acceptable quality. |
plot_qualities()
|
Plots the quality profile for an entire experiment. |
plot_taxa()
|
Plots relative distribution for taxa across samples. |
power_analysis()
|
Run a power analysis for microbe abundances from a reference sample. |
preprocess()
|
Runs preprocessing of sequencing reads. |
quality_control()
|
Workflow for basic quality assessment of the read files. |
quality_profile()
|
Get the quality profiles and base calls for each cycle across all
input files. |
read_bam()
|
Read alignments from a BAM file. |
read_blast()
|
Read a blast hit/alignment file. |
read_length()
|
Heuristic to get the median read length from a BAM file.access |
read_slimm()
|
Reads SLIMM output to a data table. |
read_slimm_coverage()
|
Reads SLIMM coverage to a data table. |
remove_reference()
|
Removes sequence that map to a given reference. |
replication_rates()
|
Estimate replication rates by the iRep method. |
select()
|
Very simple select for mbtools artifacts. Just gets a particular entry. |
silva_build_taxonomy()
|
Build the lineages for the entire SILVA database. |
slimm()
|
Quantifies abundances and coverage using SLIMM. |
slimm_files
|
The SLIMM taxonomy databases |
sra_submission()
|
Prepare submission files for the NCBI sequence read archive (SRA). |
standardize()
|
Standardize all continuous columns of a data frame. |
taxa_count()
|
Counts the reads for a specific taxonomy level. |
taxa_metrics()
|
Calculates what percentage of taxa was found in a reference set. |
taxa_quants()
|
Compares taxa quantification from a measurement to a reference ground truth. |
types()
|
Applies the specified types to a data frame-like object. |
with_classification()
|
Quantify classification rates for each taxonomic rank. |