amplicanPipelineConservative: Wraps main package functionality into one function.
In amplican: Automated analysis of CRISPR experiments

Description Usage Arguments Details Value See Also

amplicanPipelineIndexHopping is identical as amplicanPipeline except that default min_freq threshold is set to 0.15. Setting this threshold higher will decrease risks of inadequate normalization in cases of potential Index Hopping, potentially decreasing precision of true editing rate calling. Index Hopping can be mitigated with use of unique dual indexing pooling combinations. However, in cases when you might expect Index Hopping to occur you should use this function instead of amplicanPipeline.

amplicanPipelineConservative(config, fastq_folder, results_folder,
  knit_reports = TRUE, write_alignments_format = "txt",
  average_quality = 30, min_quality = 0, use_parallel = FALSE,
  scoring_matrix = Biostrings::nucleotideSubstitutionMatrix(match = 5,
  mismatch = -4, baseOnly = TRUE, type = "DNA"), gap_opening = 25,
  gap_extension = 0, fastqfiles = 0.5, primer_mismatch = 0,
  donor_mismatch = 3, PRIMER_DIMER = 30, event_filter = TRUE,
  cut_buffer = 5, promiscuous_consensus = TRUE,
  normalize = c("guideRNA", "Group"), min_freq = min_freq_default)

`config`	(string) The path to your configuration file. For example: `system.file("extdata", "config.txt", package = "amplican")`. Configuration file can contain additional columns, but first 11 columns have to follow the example config specification.
`fastq_folder`	(string) Path to FASTQ files. If not specified, FASTQ files should be in the same directory as config file.
`results_folder`	(string) Where do you want to store results? The package will create files in that folder so make sure you have writing permissions.
`knit_reports`	(boolean) whether function should "knit" all reports automatically for you (it is time consuming, be patient), when false reports will be prepared, but not knitted
`write_alignments_format`	(character vector) Whether `amplicanPipeline` should write alignments results to separate files. Alignments are also always saved as .rds object of `AlignmentsExperimentSet` class. Possible options are: "fasta" outputs alignments in fasta format where header indicates experiment ID, read id and number of reads "txt" simple format, read information followed by forward read and amplicon sequence followed by reverse read with its amplicon sequence eg.: ID: ID_1 Count: 7 ACTGAAAAA-------- ACTG-----ACTGACTG ------G-ACTG ACTGACTGACTG "None" Don't write any alignments to files. c("fasta", "txt") There are also possible combinations of above formats, pass a vector to get alignments in multiple formats.
`average_quality`	(numeric) The FASTQ file have a quality for each nucleotide, depending on sequencing technology there exist many formats. This package uses `readFastq` to parse the reads. If the average quality of the reads fall below value of `average_quality` then sequence is filtered. Default is 0.
`min_quality`	(numeric) Similar as in average_quality, but depicts the minimum quality for ALL nucleotides in given read. If one of nucleotides has quality BELLOW `min_quality`, then the sequence is filtered. Default is 20.
`use_parallel`	(boolean) Set to TRUE, if you have registered multicore back-end.
`scoring_matrix`	(matrix) Default is 'NUC44'. Pass desired matrix using `nucleotideSubstitutionMatrix`.
`gap_opening`	(numeric) The opening gap score.
`gap_extension`	(numeric) The gap extension score.
`fastqfiles`	(numeric) Normally you want to use both FASTQ files. But in some special cases, you may want to use only the forward file, or only the reverse file. Possible options: 0 Use both FASTQ files. 0.5 Use both FASTQ files, but only for one of the reads (forward or reverse) is required to have primer perfectly matched to sequence - eg. use when reverse reads are trimmed of primers, but forward reads have forward primer in the sequence. 1 Use only the forward FASTQ file. 2 Use only the reverse FASTQ file.
`primer_mismatch`	(numeric) Decide how many mismatches are allowed during primer matching of the reads, that groups reads by experiments. When `primer_mismatch = 0` no mismatches are allowed, which can increase number of unasssigned read.
`donor_mismatch`	(numeric) How many events of length 1 (mismatches, deletions and insertions of length 1) are allowed when aligning toward the donor template. This parameter is only used when donor template is specified. The higher the parameter the less strict will be algorithm accepting read as HDR. Set to 0 if only perfect alignments to the donor template marked as HDR, unadvised due to error rate of the sequencers.
`PRIMER_DIMER`	(numeric) Value specifying buffer for PRIMER DIMER detection. For a given read it will be recognized as PRIMER DIMER when alignment will introduce gap of size bigger than: `length of amplicon - (lengths of PRIMERS + PRIMER_DIMER value)`
`event_filter`	(logical) Whether detection of offtarget reads, should be enabled.
`cut_buffer`	The number of bases by which extend expected cut sites (specified as UPPER case letters in the amplicon) in 5' and 3' directions.
`promiscuous_consensus`	(boolean) Whether rules of `amplicanConsensus` should be `promiscuous`. When promiscuous, we allow indels that have no confirmation on the other strand.
`normalize`	(character vector) If column 'Control' in config table has all FALSE/0 values then normalization is skipped. Otherwise, normalization is strict, which means events that are found in 'Control' TRUE group will be removed in 'Control' FALSE group. This parameter by default uses columns 'guideRNA' and 'Group' to impose additional restrictions on normalized events eg. only events created by the same 'guideRNA' in the same 'Group' will be normalized.
`min_freq`	(numeric) All events below this frequency are treated as sequencing errors and rejected. This parameter is used during normalization through `amplicanNormalize`.