cdsfile2rbh: cdsfile2rbh
In kullrich/CRBHits: Conditional reciprocal best hits (CRBHits) in R

cdsfile2rbh

R Documentation

cdsfile2rbh

Description

This function calculates (conditional-)reciprocal best hit (CRBHit) pairs from two CDS fasta files. CRBHit pairs were introduced by Aubry S, Kelly S et al. (2014). Sequence searches are performed with last Kiełbasa, SM et al. (2011) [default] or with mmseqs2 Steinegger, M and Soeding, J (2017) or with diamond Buchfink, B et al. (2021). If one specifies cdsfile1 and cdsfile2 as the same input a selfblast is conducted.

Usage

cdsfile2rbh(
  cdsfile1,
  cdsfile2,
  searchtool = "last",
  lastpath = paste0(find.package("CRBHits"), "/extdata/last-1542/bin/"),
  lastD = 1e+06,
  mmseqs2path = NULL,
  mmseqs2sensitivity = 5.7,
  diamondpath = NULL,
  diamondsensitivity = "--sensitive",
  diamondmaxtargetseqs = "-k0",
  outpath = "/tmp",
  crbh = TRUE,
  keepSingleDirection = FALSE,
  eval = 0.001,
  qcov = 0,
  tcov = 0,
  pident = 0,
  alnlen = 0,
  rost1999 = FALSE,
  filter = NULL,
  plotCurve = FALSE,
  fit.type = "mean",
  fit.varweight = 0.1,
  fit.min = 5,
  longest.isoform = FALSE,
  isoform.source = "NCBI",
  threads = 1,
  remove = TRUE,
  shorten1 = FALSE,
  frame1 = 1,
  framelist1 = NULL,
  genetic.code1 = NULL,
  shorten2 = FALSE,
  frame2 = 1,
  framelist2 = NULL,
  genetic.code2 = NULL
)

Arguments

`cdsfile1`	cds1 fasta file [mandatory]
`cdsfile2`	cds2 fasta file [mandatory]
`searchtool`	specify sequence search algorithm last, mmseqs2 or diamond [default: last]
`lastpath`	specify the PATH to the last binaries [default: /extdata/last-1542/bin/]
`lastD`	last option D: query letters per random alignment [default: 1e6]
`mmseqs2path`	specify the PATH to the mmseqs2 binaries [default: NULL]
`mmseqs2sensitivity`	specify the sensitivity option of mmseqs2 [default: 5.7]
`diamondpath`	specify the PATH to the diamond binaries [default: NULL]
`diamondsensitivity`	specify the sensitivity option of diamond [default: –sensitive]
`diamondmaxtargetseqs`	specify the maximum number of target sequences per query option of diamond [default: -k0]
`outpath`	specify the output PATH [default: /tmp]
`crbh`	specify if conditional-reciprocal hit pairs should be retained as secondary hits [default: TRUE]
`keepSingleDirection`	specify if single direction secondary hit pairs should be retained [default: FALSE]
`eval`	evalue [default: 1e-3]
`qcov`	query coverage [default: 0.0]
`tcov`	target coverage [default: 0.0]
`pident`	percent identity [default: 0.0]
`alnlen`	alignment length [default: 0.0]
`rost1999`	specify if hit pairs should be filter by equation 2 of Rost 1999 [default: FALSE]
`filter`	specify additional custom filters as list to be applied on hit pairs [default: NULL]
`plotCurve`	specify if crbh fitting curve should be plotted [default: FALSE]
`fit.type`	specify if mean or median should be used for fitting [default: mean]
`fit.varweight`	factor for fitting function to consider neighborhood [default: 0.1]
`fit.min`	specify minimum neighborhood alignment length [default: 5]
`longest.isoform`	specify if cds sequences should be removed to the longest isoform (only possible if data was accessed from NCBI or ENSEMBL) [default: FALSE]
`isoform.source`	specify cds sequences source (either NCBI or ENSEMBL) [default: NCBI]
`threads`	number of parallel threads [default: 1]
`remove`	specify if last result files should be removed [default: TRUE]
`shorten1`	shorten all sequences to multiple of three [default: FALSE]
`frame1`	indicates the first base of a the first codon [default: 1]
`framelist1`	supply vector of frames for each entry [default: NULL]
`genetic.code1`	The genetic code to use for the translation of codons into Amino Acid letters [default: NULL]
`shorten2`	shorten all sequences to multiple of three [default: FALSE]
`frame2`	indicates the first base of a the first codon [default: 1]
`framelist2`	supply vector of frames for each entry [default: NULL]
`genetic.code2`	The genetic code to use for the translation of codons into Amino Acid letters [default: NULL]

Value

List of three (crbh=FALSE)
1: $crbh.pairs
2: $crbh1 matrix; query > target
3: $crbh2 matrix; target > query

List of four (crbh=TRUE)
1: $crbh.pairs
2: $crbh1 matrix; query > target
3: $crbh2 matrix; target > query
4: $rbh1_rbh2_fit; evalue fitting function

Author(s)

Kristian K Ullrich

References

Aubry S, Kelly S et al. (2014) Deep Evolutionary Comparison of Gene Expression Identifies Parallel Recruitment of Trans-Factors in Two Independent Origins of C4 Photosynthesis. PLOS Genetics, 10(6) e1004365.

Kiełbasa, SM et al. (2011) Adaptive seeds tame genomic sequence comparison. Genome research, 21(3), 487-493.

Steinegger, M and Soeding, J. (2017). MMseqs2 enables sensitive protein sequence searching for the analysis of massive data sets. Nature Biotechnology, 35, 1026-1028.

Rost B. (1999). Twilight zone of protein sequence alignments. Protein Engineering, 12(2), 85-94.

Examples

## compile last-1542 within CRBHits
CRBHits::make_last()
## load example sequence data
athfile <- system.file("fasta", "ath.cds.fasta.gz", package="CRBHits")
alyfile <- system.file("fasta", "aly.cds.fasta.gz", package="CRBHits")
## get CRBHit pairs
ath_aly_crbh <- cdsfile2rbh(
    cdsfile1=athfile,
    cdsfile2=alyfile,
    plotCurve=TRUE)
dim(ath_aly_crbh$crbh.pairs)
## get classical reciprocal best hit (RBHit) pairs
ath_aly_rbh <- cdsfile2rbh(
    cdsfile1=athfile,
    cdsfile2=alyfile,
    crbh=FALSE)
dim(ath_aly_rbh$crbh.pairs)
## selfblast
ath_selfblast_crbh <- cdsfile2rbh(
    cdsfile1=athfile,
    cdsfile2=athfile,
    plotCurve=TRUE)
## see ?cds2rbh for more examples

kullrich/CRBHits documentation built on March 29, 2024, 11:34 a.m.