codon_usage_exp: Codon analysis for ORFik experiment

codon_usage_expR Documentation

Codon analysis for ORFik experiment

Description

Per AA / codon, analyse the coverage, get a multitude of features. For both A sites and P-sites (Input reads must be P-sites for now) This function takes inspiration from the codonDT paper, and among others returns the negative binomial estimates, but in addition many other features.

Usage

codon_usage_exp(
  df,
  reads,
  cds = loadRegion(df, "cds", filterTranscripts(df)),
  mrna = loadRegion(df, "mrna", names(cds)),
  filter_cds_mod3 = TRUE,
  filter_table = assay(countTable(df, type = "summarized")[names(cds)]),
  faFile = df@fafile,
  min_counts_cds_filter = max(min(quantile(filter_table, 0.5), 1000), 1000),
  with_A_sites = TRUE,
  code = GENETIC_CODE,
  aligned_position = "center"
)

Arguments

df

an ORFik experiment

reads

either a single library (GRanges, GAlignment, GAlignmentPairs), or a list of libraries returned from outputLibs(df) with p-sites. If list, the list must have names coresponding to the library names.

cds

a GRangesList, the coding sequences, default: loadRegion(df, "cds", filterTranscripts(df)), longest isoform per gene.

mrna

a GRangesList, the full mRNA sequences (matching by names the cds sequences), default: loadRegion(df, "mrna", names(cds)).

filter_cds_mod3

logical, default TRUE. Remove all ORFs that are not mod3, this speeds up the computation a lot, and usually removes malformed ORFs you would not want anyway.

filter_table

an numeric(integer) matrix, where rownames are the names of the full set of mRNA transcripts. This will be subsetted to the cds subset you use. Then CDSs are filtered from this table by the 'min_counts_cds_filter' argument.

faFile

FaFile, BSgenome, fasta/index file path or an ORFik experiment. This file is usually used to find the transcript sequences from some GRangesList.

min_counts_cds_filter

numeric, default: max(min(quantile(filter_table, 0.50), 100), 100). Minimum number of counts from the 'filter_table' argument.

with_A_sites

logical, default TRUE. Not used yet, will also return A site scores.

code

a named character vector of size 64. Default: GENETIC_CODE. Change if organism does not use the standard code.

aligned_position

what positions should be taken to calculate per-codon coverage. By default: "center", meaning that positions -1,0,1 will be taken. Alternative: "left", then positions 0,1,2 are taken.

Details

The primary column to use is "mean_txNorm", this is the fair normalized score.

Value

a data.table of rows per codon / AA. All values are given per library, per site (A or P), sorted by the mean_txNorm_percentage column of the first library in the set, the columns are:

  • variable (character)Library name

  • seq (character)Amino acid:codon

  • sum (integer)total counts per seq

  • sum_txNorm (integer)total counts per seq normalized per tx

  • var (numeric)variance of total counts per seq

  • N (integer)total number of codons of that type

  • mean_txNorm (numeric)Default use output, the fair codon usage, normalized both for gene and genome level for codon and read counts

  • ...

  • alpha (numeric)dirichlet alpha MOM estimator (imagine mean and variance of probability in 1 value, the lower the value, the higher the variance, mean is decided by the relative value between samples)

  • sum_txNorm (integer)total counts per seq normalized per tx

  • relative_to_max_score (integer)Percentage use of codon

  • type (factor(character))Either "P" or "A"

References

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7196831/

See Also

Other codon: codon_usage(), codon_usage_plot()

Examples

df <- ORFik.template.experiment()[9:10,] # Subset to 2 Ribo-seq libs
## For single library
res <- codon_usage_exp(df, fimport(filepath(df[1,], "pshifted")),
                 min_counts_cds_filter = 10)
# mean_txNorm is adviced scoring column
# codon_usage_plot(res, res$mean_txNorm)
# Default for plot function is the percentage scaled version of mean_txNorm
# codon_usage_plot(res) # This gives check error
## For multiple libs
res2 <- codon_usage_exp(df, outputLibs(df, type = "pshifted", output.mode = "list"),
                 min_counts_cds_filter = 10)
# codon_usage_plot(res2)

Roleren/ORFik documentation built on Oct. 19, 2024, 7:37 a.m.