View source: R/Filter_function.R
Filter_function | R Documentation |
Sequenced data of taxonomy&gene still remains some sequencing error which we needed to be wiped off before analyzing. Here we provide function including four formats to wipe them clean.
Filter_function(input, threshold, format, report = TRUE)
input |
Data frame of absolute abundance of standard OTU table,with the first column of OTUID and the final column of taxonomy annotation. If your data frame is gene table or not a standard OTU table, please manually transformed into a standard input data frame. |
threshold |
threshold of filter.Relative abundance for format 1 and 4, reads number for format 2, sample size for format 3 |
format |
1:filter OTU/gene below overall-sample relative abundance threshold(<) 2:filter OTU/gene below overall-sample reads threshold(<) 3:filter OTU/gene reads 0 over threshold sample size(>) 4:filter OTU/gene below relative abundance threshold in each sample(<) |
report |
Logical. If print report to console. Default:TRUE |
Dataframe of OTU/gene in format of absolute abundacne(reads) or relative abundance(%)
Wang Ningqi
### Data frame with absolute abundance (reads)###
### And first column of OTUID and last column of taxonomy ###
data(testotu)
#### If your data frame does not contain the OTUID column or taxonomy column,
#### you can add a simulated column to fit the input format like testotu ##
### 1. Filter OTU with total relative abundance below 0.0001###
filtered_otu <- Filter_function(
input = testotu,
threshold = 0.0001,
format = 1
)
### 2. Filter OTU with total reads below 20 ###
filtered_otu <- Filter_function(
input = testotu,
threshold = 20,
format = 2
)
### 3. Filter OTU reads 0 over (>=) 11 samples ###
filtered_otu <- Filter_function(
input = testotu,
threshold = 11,
format = 3
)
### 4. Filter OTU with relative abundance below 0.0001 in each sample ###
filtered_otu <- Filter_function(
input = testotu,
threshold = 0.0001,
format = 4
)
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