Provided by: fastp_0.23.4+dfsg-1_amd64 bug

NAME

       fastp - Ultra-fast all-in-one FASTQ preprocessor

DESCRIPTION

       fastp: an ultra-fast all-in-one FASTQ preprocessor version 0.23.0 usage: fastp [options] ...  options:

       -i, --in1
              read1 input file name (string [=])

       -o, --out1
              read1 output file name (string [=])

       -I, --in2
              read2 input file name (string [=])

       -O, --out2
              read2 output file name (string [=])

       --unpaired1
              for  PE  input,  if  read1 passed QC but read2 not, it will be written to unpaired1. Default is to
              discard it. (string [=])

       --unpaired2
              for PE input, if read2 passed QC but read1 not, it will be written to unpaired2. If --unpaired2 is
              same as --unpaired1 (default mode), both unpaired reads will be written to this same file. (string
              [=])

       --overlapped_out
              for each read pair, output the overlapped region if it has no any mismatched base. (string [=])

       --failed_out
              specify the file to store reads that cannot pass the filters. (string [=])

       -m, --merge
              for paired-end input, merge each pair of reads into a single read  if  they  are  overlapped.  The
              merged reads will be written to the file given by --merged_out, the unmerged reads will be written
              to the files specified by --out1 and --out2. The merging mode is disabled by default.

       --merged_out
              in  the  merging mode, specify the file name to store merged output, or specify --stdout to stream
              the merged output (string [=])

       --include_unmerged
              in the merging mode, write the unmerged or unpaired  reads  to  the  file  specified  by  --merge.
              Disabled by default.

       -6, --phred64
              indicate  the  input  is  using phred64 scoring (it'll be converted to phred33, so the output will
              still be phred33)

       -z, --compression
              compression level for gzip output (1 ~ 9). 1 is fastest, 9 is smallest, default is 4. (int [=4])

       --stdin
              input from STDIN. If the STDIN is interleaved paired-end FASTQ, please also add --interleaved_in.

       --stdout
              stream passing-filters reads to STDOUT. This option will result in interleaved  FASTQ  output  for
              paired-end output. Disabled by default.

       --interleaved_in
              indicate  that  <in1>  is  an  interleaved  FASTQ which contains both read1 and read2. Disabled by
              default.

       --reads_to_process
              specify how many reads/pairs to be processed. Default 0 means process all reads. (int [=0])

       --dont_overwrite
              don't overwrite existing files. Overwritting is allowed by default.

       --fix_mgi_id
              the MGI FASTQ ID format is not compatible with many BAM operation tools, enable this option to fix
              it.

       -V, --verbose
              output verbose log information (i.e. when every 1M reads are processed).

       -A, --disable_adapter_trimming
              adapter trimming is enabled by default. If this option is specified, adapter trimming is disabled

       -a, --adapter_sequence
              the adapter for read1. For SE data, if not specified, the adapter will be  auto-detected.  For  PE
              data, this is used if R1/R2 are found not overlapped. (string [=auto])

       --adapter_sequence_r2
              the  adapter  for  read2  (PE  data  only). This is used if R1/R2 are found not overlapped. If not
              specified, it will be the same as <adapter_sequence> (string [=auto])

       --adapter_fasta
              specify a FASTA file to trim both read1 and read2 (if PE) by all the sequences in this FASTA  file
              (string [=])

       --detect_adapter_for_pe
              by  default,  the  auto-detection  for  adapter  is for SE data input only, turn on this option to
              enable it for PE data.

       -f, --trim_front1
              trimming how many bases in front for read1, default is 0 (int [=0])

       -t, --trim_tail1
              trimming how many bases in tail for read1, default is 0 (int [=0])

       -b, --max_len1
              if read1 is longer than max_len1, then trim read1 at its tail to make  it  as  long  as  max_len1.
              Default 0 means no limitation (int [=0])

       -F, --trim_front2
              trimming how many bases in front for read2. If it's not specified, it will follow read1's settings
              (int [=0])

       -T, --trim_tail2
              trimming  how many bases in tail for read2. If it's not specified, it will follow read1's settings
              (int [=0])

       -B, --max_len2
              if read2 is longer than max_len2, then trim read2 at its tail to make  it  as  long  as  max_len2.
              Default 0 means no limitation. If it's not specified, it will follow read1's settings (int [=0])

       -D, --dedup
              enable deduplication to drop the duplicated reads/pairs

       --dup_calc_accuracy
              accuracy level to calculate duplication (1~6), higher level uses more memory (1G, 2G, 4G, 8G, 16G,
              24G). Default 1 for no-dedup mode, and 3 for dedup mode. (int [=0])

       --dont_eval_duplication
              don't evaluate duplication rate to save time and use less memory.

       -g, --trim_poly_g
              force   polyG   tail   trimming,  by  default  trimming  is  automatically  enabled  for  Illumina
              NextSeq/NovaSeq data

       --poly_g_min_len
              the minimum length to detect polyG in the read tail. 10 by default. (int [=10])

       -G, --disable_trim_poly_g
              disable  polyG  tail  trimming,  by  default  trimming  is  automatically  enabled  for   Illumina
              NextSeq/NovaSeq data

       -x, --trim_poly_x
              enable polyX trimming in 3' ends.

       --poly_x_min_len
              the minimum length to detect polyX in the read tail. 10 by default. (int [=10])

       -5, --cut_front
              move  a sliding window from front (5') to tail, drop the bases in the window if its mean quality <
              threshold, stop otherwise.

       -3, --cut_tail
              move a sliding window from tail (3') to front, drop the bases in the window if its mean quality  <
              threshold, stop otherwise.

       -r, --cut_right
              move  a  sliding window from front to tail, if meet one window with mean quality < threshold, drop
              the bases in the window and the right part, and then stop.

       -W, --cut_window_size
              the window size option shared by cut_front, cut_tail or cut_sliding.  Range:  1~1000,  default:  4
              (int [=4])

       -M, --cut_mean_quality
              the  mean  quality  requirement  option  shared by cut_front, cut_tail or cut_sliding. Range: 1~36
              default: 20 (Q20) (int [=20])

       --cut_front_window_size
              the window size option of cut_front, default to cut_window_size if not specified (int [=4])

       --cut_front_mean_quality
              the mean quality requirement option for cut_front, default to cut_mean_quality  if  not  specified
              (int [=20])

       --cut_tail_window_size
              the window size option of cut_tail, default to cut_window_size if not specified (int [=4])

       --cut_tail_mean_quality
              the  mean  quality  requirement  option for cut_tail, default to cut_mean_quality if not specified
              (int [=20])

       --cut_right_window_size
              the window size option of cut_right, default to cut_window_size if not specified (int [=4])

       --cut_right_mean_quality
              the mean quality requirement option for cut_right, default to cut_mean_quality  if  not  specified
              (int [=20])

       -Q, --disable_quality_filtering
              quality  filtering  is  enabled  by  default.  If  this  option is specified, quality filtering is
              disabled

       -q, --qualified_quality_phred
              the quality value that a base is qualified. Default 15 means phred  quality  >=Q15  is  qualified.
              (int [=15])

       -u, --unqualified_percent_limit
              how many percents of bases are allowed to be unqualified (0~100). Default 40 means 40% (int [=40])

       -n, --n_base_limit
              if  one  read's  number of N base is >n_base_limit, then this read/pair is discarded. Default is 5
              (int [=5])

       -e, --average_qual
              if one read's average quality score <avg_qual, then this read/pair is discarded. Default  0  means
              no requirement (int [=0])

       -L, --disable_length_filtering
              length filtering is enabled by default. If this option is specified, length filtering is disabled

       -l, --length_required
              reads shorter than length_required will be discarded, default is 15. (int [=15])

       --length_limit
              reads longer than length_limit will be discarded, default 0 means no limitation. (int [=0])

       -y, --low_complexity_filter
              enable  low  complexity  filter.  The  complexity  is  defined  as  the percentage of base that is
              different from its next base (base[i] != base[i+1]).

       -Y, --complexity_threshold
              the threshold for low complexity filter (0~100). Default is 30,  which  means  30%  complexity  is
              required. (int [=30])

       --filter_by_index1
              specify  a  file  contains  a  list of barcodes of index1 to be filtered out, one barcode per line
              (string [=])

       --filter_by_index2
              specify a file contains a list of barcodes of index2 to be filtered  out,  one  barcode  per  line
              (string [=])

       --filter_by_index_threshold
              the allowed difference of index barcode for index filtering, default 0 means completely identical.
              (int [=0])

       -c, --correction
              enable base correction in overlapped regions (only for PE data), default is disabled

       --overlap_len_require
              the  minimum  length  to  detect  overlapped region of PE reads. This will affect overlap analysis
              based PE merge, adapter trimming and correction. 30 by default. (int [=30])

       --overlap_diff_limit
              the maximum number of mismatched bases to detect overlapped region of PE reads. This  will  affect
              overlap analysis based PE merge, adapter trimming and correction. 5 by default. (int [=5])

       --overlap_diff_percent_limit
              the  maximum  percentage  of  mismatched  bases to detect overlapped region of PE reads. This will
              affect overlap analysis based PE merge, adapter trimming and correction.  Default  20  means  20%.
              (int [=20])

       -U, --umi
              enable unique molecular identifier (UMI) preprocessing

       --umi_loc
              specify the location of UMI, can be (index1/index2/read1/read2/per_index/per_read, default is none
              (string [=])

       --umi_len
              if the UMI is in read1/read2, its length should be provided (int [=0])

       --umi_prefix
              if  specified,  an  underline will be used to connect prefix and UMI (i.e. prefix=UMI, UMI=AATTCG,
              final=UMI_AATTCG). No prefix by default (string [=])

       --umi_skip
              if the UMI is in read1/read2, fastp can skip several bases following UMI, default is 0 (int [=0])

       -p, --overrepresentation_analysis
              enable overrepresented sequence analysis.

       -P, --overrepresentation_sampling
              one in (--overrepresentation_sampling) reads will  be  computed  for  overrepresentation  analysis
              (1~10000), smaller is slower, default is 20. (int [=20])

       -j, --json
              the json format report file name (string [=fastp.json])

       -h, --html
              the html format report file name (string [=fastp.html])

       -R, --report_title
              should be quoted with ' or ", default is "fastp report" (string [=fastp report])

       -w, --thread
              worker thread number, default is 3 (int [=3])

       -s, --split
              split  output  by  limiting  total split file number with this option (2~999), a sequential number
              prefix will be added to output name ( 0001.out.fq, 0002.out.fq...), disabled by default (int [=0])

       -S, --split_by_lines
              split output by limiting lines of each file with this option(>=1000), a sequential  number  prefix
              will be added to output name ( 0001.out.fq, 0002.out.fq...), disabled by default (long [=0])

       -d, --split_prefix_digits
              the  digits for the sequential number padding (1~10), default is 4, so the filename will be padded
              as 0001.xxx, 0 to disable padding (int [=4])

       --cut_by_quality5
              DEPRECATED, use --cut_front instead.

       --cut_by_quality3
              DEPRECATED, use --cut_tail instead.

       --cut_by_quality_aggressive
              DEPRECATED, use --cut_right instead.

       --discard_unmerged
              DEPRECATED, no effect now, see the introduction for merging.

       -?, --help
              print this message

AUTHOR

        This manpage was written by Nilesh Patra for the Debian distribution and
        can be used for any other usage of the program.

fastp 0.23.0                                      October 2021                                          FASTP(1)