--- a +++ b/man/generator_fasta_lm.Rd @@ -0,0 +1,167 @@ +% Generated by roxygen2: do not edit by hand +% Please edit documentation in R/generator_lm.R +\name{generator_fasta_lm} +\alias{generator_fasta_lm} +\title{Language model generator for fasta/fastq files} +\usage{ +generator_fasta_lm( + path_corpus, + format = "fasta", + batch_size = 256, + maxlen = 250, + max_iter = 10000, + vocabulary = c("a", "c", "g", "t"), + verbose = FALSE, + shuffle_file_order = FALSE, + step = 1, + seed = 1234, + shuffle_input = FALSE, + file_limit = NULL, + path_file_log = NULL, + reverse_complement = FALSE, + output_format = "target_right", + ambiguous_nuc = "zeros", + use_quality_score = FALSE, + proportion_per_seq = NULL, + padding = TRUE, + added_label_path = NULL, + add_input_as_seq = NULL, + skip_amb_nuc = NULL, + max_samples = NULL, + concat_seq = NULL, + target_len = 1, + file_filter = NULL, + use_coverage = NULL, + proportion_entries = NULL, + sample_by_file_size = FALSE, + n_gram = NULL, + n_gram_stride = 1, + add_noise = NULL, + return_int = FALSE, + reshape_xy = NULL +) +} +\arguments{ +\item{path_corpus}{Input directory where fasta files are located or path to single file ending with fasta or fastq +(as specified in format argument). Can also be a list of directories and/or files.} + +\item{format}{File format, either \code{"fasta"} or \code{"fastq"}.} + +\item{batch_size}{Number of samples in one batch.} + +\item{maxlen}{Length of predictor sequence.} + +\item{max_iter}{Stop after \code{max_iter} number of iterations failed to produce a new batch.} + +\item{vocabulary}{Vector of allowed characters. Characters outside vocabulary get encoded as specified in \code{ambiguous_nuc}.} + +\item{verbose}{Whether to show messages.} + +\item{shuffle_file_order}{Logical, whether to go through files randomly or sequentially.} + +\item{step}{How often to take a sample.} + +\item{seed}{Sets seed for \code{set.seed} function for reproducible results.} + +\item{shuffle_input}{Whether to shuffle entries in every fasta/fastq file before extracting samples.} + +\item{file_limit}{Integer or \code{NULL}. If integer, use only specified number of randomly sampled files for training. Ignored if greater than number of files in \code{path}.} + +\item{path_file_log}{Write name of files to csv file if path is specified.} + +\item{reverse_complement}{Boolean, for every new file decide randomly to use original data or its reverse complement.} + +\item{output_format}{Determines shape of output tensor for language model. +Either \code{"target_right"}, \code{"target_middle_lstm"}, \code{"target_middle_cnn"} or \code{"wavenet"}. +Assume a sequence \code{"AACCGTA"}. Output correspond as follows +\itemize{ +\item \verb{"target_right": X = "AACCGT", Y = "A"} +\item \verb{"target_middle_lstm": X = (X_1 = "AAC", X_2 = "ATG"), Y = "C"} (note reversed order of X_2) +\item \verb{"target_middle_cnn": X = "AACGTA", Y = "C"} +\item \verb{"wavenet": X = "AACCGT", Y = "ACCGTA"} +}} + +\item{ambiguous_nuc}{How to handle nucleotides outside vocabulary, either \code{"zero"}, \code{"discard"}, \code{"empirical"} or \code{"equal"}. +\itemize{ +\item If \code{"zero"}, input gets encoded as zero vector. +\item If \code{"equal"}, input is repetition of \code{1/length(vocabulary)}. +\item If \code{"discard"}, samples containing nucleotides outside vocabulary get discarded. +\item If \code{"empirical"}, use nucleotide distribution of current file. +}} + +\item{use_quality_score}{Whether to use fastq quality scores. If TRUE input is not one-hot-encoding but corresponds to probabilities. +For example (0.97, 0.01, 0.01, 0.01) instead of (1, 0, 0, 0).} + +\item{proportion_per_seq}{Numerical value between 0 and 1. Proportion of sequence to take samples from (use random subsequence).} + +\item{padding}{Whether to pad sequences too short for one sample with zeros.} + +\item{added_label_path}{Path to file with additional input labels. Should be a csv file with one column named "file". Other columns should correspond to labels.} + +\item{add_input_as_seq}{Boolean vector specifying for each entry in \code{added_label_path} if rows from csv should be encoded as a sequence or used directly. +If a row in your csv file is a sequence this should be \code{TRUE}. For example you may want to add another sequence, say ACCGT. Then this would correspond to 1,2,2,3,4 in +csv file (if vocabulary = c("A", "C", "G", "T")). If \code{add_input_as_seq} is \code{TRUE}, 12234 gets one-hot encoded, so added input is a 3D tensor. If \code{add_input_as_seq} is +\code{FALSE} this will feed network just raw data (a 2D tensor).} + +\item{skip_amb_nuc}{Threshold of ambiguous nucleotides to accept in fasta entry. Complete entry will get discarded otherwise.} + +\item{max_samples}{Maximum number of samples to use from one file. If not \code{NULL} and file has more than \code{max_samples} samples, will randomly choose a +subset of \code{max_samples} samples.} + +\item{concat_seq}{Character string or \code{NULL}. If not \code{NULL} all entries from file get concatenated to one sequence with \code{concat_seq} string between them. +Example: If 1.entry AACC, 2. entry TTTG and \code{concat_seq = "ZZZ"} this becomes AACCZZZTTTG.} + +\item{target_len}{Number of nucleotides to predict at once for language model.} + +\item{file_filter}{Vector of file names to use from path_corpus.} + +\item{use_coverage}{Integer or \code{NULL}. If not \code{NULL}, use coverage as encoding rather than one-hot encoding and normalize. +Coverage information must be contained in fasta header: there must be a string \code{"cov_n"} in the header, where \code{n} is some integer.} + +\item{proportion_entries}{Proportion of fasta entries to keep. For example, if fasta file has 50 entries and \code{proportion_entries = 0.1}, +will randomly select 5 entries.} + +\item{sample_by_file_size}{Sample new file weighted by file size (bigger files more likely).} + +\item{n_gram}{Integer, encode target not nucleotide wise but combine n nucleotides at once. For example for \verb{n=2, "AA" -> (1, 0,..., 0),} +\verb{"AC" -> (0, 1, 0,..., 0), "TT" -> (0,..., 0, 1)}, where the one-hot vectors have length \code{length(vocabulary)^n}.} + +\item{n_gram_stride}{Step size for n-gram encoding. For AACCGGTT with \code{n_gram = 4} and \code{n_gram_stride = 2}, generator encodes +\verb{(AACC), (CCGG), (GGTT)}; for \code{n_gram_stride = 4} generator encodes \verb{(AACC), (GGTT)}.} + +\item{add_noise}{\code{NULL} or list of arguments. If not \code{NULL}, list must contain the following arguments: \code{noise_type} can be \code{"normal"} or \code{"uniform"}; +optional arguments \code{sd} or \code{mean} if noise_type is \code{"normal"} (default is \code{sd=1} and \code{mean=0}) or \verb{min, max} if \code{noise_type} is \code{"uniform"} +(default is \verb{min=0, max=1}).} + +\item{return_int}{Whether to return integer encoding or one-hot encoding.} + +\item{reshape_xy}{Can be a list of functions to apply to input and/or target. List elements (containing the reshape functions) +must be called x for input or y for target and each have arguments called x and y. For example: +\code{reshape_xy = list(x = function(x, y) {return(x+1)}, y = function(x, y) {return(x+y)})} . +For rds generator needs to have an additional argument called sw.} +} +\value{ +A generator function. +} +\description{ +Iterates over folder containing fasta/fastq files and produces encoding of predictor sequences +and target variables. Will take a sequence of fixed size and use some part of sequence as input and other part as target. +} +\examples{ +\dontshow{if (reticulate::py_module_available("tensorflow")) (if (getRversion() >= "3.4") withAutoprint else force)(\{ # examplesIf} +# create dummy fasta files +path_input_1 <- tempfile() +dir.create(path_input_1) +create_dummy_data(file_path = path_input_1, + num_files = 2, + seq_length = 8, + num_seq = 1, + vocabulary = c("a", "c", "g", "t")) + +gen <- generator_fasta_lm(path_corpus = path_input_1, batch_size = 2, + maxlen = 7) +z <- gen() +dim(z[[1]]) +z[[2]] +\dontshow{\}) # examplesIf} +}