read_sequences_from_fastq | R Documentation |
read_sequences_from_fastq
read_sequences_from_fastq
get the sequences
from a fastq file, it completely ignores the quality scores
read_sequences_from_fastq(
fastq_file,
force_to_upper = TRUE,
skip_n_reads = 0,
max_n_reads = -1,
output_quality = TRUE,
quality_offset = 33,
bp = MulticoreParam()
)
fastq_file |
location of the fastq file |
force_to_upper |
whether to transform sequences to upper case, default to TRUE |
skip_n_reads |
number of reads to skip, default to 0 |
max_n_reads |
maximum number of reads to read, default to -1 (all) |
output_quality |
whether to output the quality scores, default to TRUE |
quality_offset |
the quality offset to use, default to 33 |
bp |
BiocParallel backend to use for parallelization |
will return a list of sequences, with qualities as attribute
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