Provided by: subread_1.6.0+dfsg-1_amd64 
NAME
featureCounts - a highly efficient and accurate read summarization program
SYNOPSIS
featureCounts [options] -a <annotation_file> -o <output_file> input_file1 [input_file2]
...
DESCRIPTION
Version 1.6.0
## Mandatory arguments:
-a <string>
Name of an annotation file. GTF/GFF format by default. See -F option for more
format information. Inbuilt annotations (SAF format) is available in 'annotation'
directory of the package.
-o <string>
Name of the output file including read counts. A separate file including summary
statistics of counting results is also included in the output ('<string>.summary')
input_file1 [input_file2] ...
A list of SAM or BAM format files. They can be
either name or location sorted. If no files provided,
<stdin> input is expected. Location-sorted paired-end reads are automatically
sorted by read names.
## Optional arguments: # Annotation
-F <string>
Specify format of the provided annotation file. Acceptable formats include 'GTF'
(or compatible GFF format) and 'SAF'. 'GTF' by default. For SAF format, please
refer to Users Guide.
-t <string>
Specify feature type in GTF annotation. 'exon' by default. Features used for read
counting will be extracted from annotation using the provided value.
-g <string>
Specify attribute type in GTF annotation. 'gene_id' by default. Meta-features used
for read counting will be extracted from annotation using the provided value.
-A <string>
Provide a chromosome name alias file to match chr names in annotation with those in
the reads. This should be a twocolumn comma-delimited text file. Its first column
should include chr names in the annotation and its second column should include chr
names in the reads. Chr names are case sensitive. No column header should be
included in the file.
# Level of summarization
-f Perform read counting at feature level (eg. counting reads for exons rather than
genes).
# Overlap between reads and features
-O Assign reads to all their overlapping meta-features (or features if -f is
specified).
--minOverlap <int>
Minimum number of overlapping bases in a read that is required for read assignment.
1 by default. Number of overlapping bases is counted from both reads if paired end.
If a negative value is provided, then a gap of up to specified size will be allowed
between read and the feature that the read is assigned to.
--fracOverlap <float> Minimum fraction of overlapping bases in a read that is
required for read assignment. Value should be within range [0,1]. 0 by default.
Number of overlapping bases is counted from both reads if paired end. Both this
option and '--minOverlap' option need to be satisfied for read assignment.
--fracOverlapFeature <float> Minimum fraction of bases included in a feature
that is required for overlapping with a read or a readpair. Value should be within
range [0,1]. 0 by default.
--largestOverlap
Assign reads to a meta-feature/feature that has the largest number of overlapping
bases.
--readExtension5 <int> Reads are extended upstream by <int> bases from their
5' end.
--readExtension3 <int> Reads are extended upstream by <int> bases from their
3' end.
--read2pos <5:3>
Reduce reads to their 5' most base or 3' most base. Read counting is then performed
based on the single base the read is reduced to.
# Multi-mapping reads
-M Multi-mapping reads will also be counted. For a multimapping read, all its reported
alignments will be counted. The 'NH' tag in BAM/SAM input is used to detect
multi-mapping reads.
# Fractional counting
--fraction
Assign fractional counts to features. This option must be used together with '-M'
or '-O' or both. When '-M' is specified, each reported alignment from a
multi-mapping read (identified via 'NH' tag) will carry a fractional count of 1/x,
instead of 1 (one), where x is the total number of alignments reported for the same
read. When '-O' is specified, each overlapping feature will receive a fractional
count of 1/y, where y is the total number of features overlapping with the read.
When both '-M' and '-O' are specified, each alignment will carry a fractional count
of 1/(x*y).
# Read filtering
-Q <int>
The minimum mapping quality score a read must satisfy in order to be counted. For
paired-end reads, at least one end should satisfy this criteria. 0 by default.
--splitOnly
Count split alignments only (ie. alignments with CIGAR string containing 'N'). An
example of split alignments is exon-spanning reads in RNA-seq data.
--nonSplitOnly
If specified, only non-split alignments (CIGAR strings do not contain letter 'N')
will be counted. All the other alignments will be ignored.
--primary
Count primary alignments only. Primary alignments are identified using bit 0x100 in
SAM/BAM FLAG field.
--ignoreDup
Ignore duplicate reads in read counting. Duplicate reads are identified using bit
Ox400 in BAM/SAM FLAG field. The whole read pair is ignored if one of the reads is
a duplicate read for paired end data.
# Strandness
-s <int>
Perform strand-specific read counting. Acceptable values: 0 (unstranded), 1
(stranded) and 2 (reversely stranded). 0 by default.
# Exon-exon junctions
-J Count number of reads supporting each exon-exon junction. Junctions were
identified from those exon-spanning reads in the input (containing 'N' in CIGAR
string). Counting results are saved to a file named '<output_file>.jcounts'
-G <string>
Provide the name of a FASTA-format file that contains the reference sequences used
in read mapping that produced the provided SAM/BAM files. This optional argument
can be used with '-J' option to improve read counting for junctions.
# Parameters specific to paired end reads
-p If specified, fragments (or templates) will be counted instead of reads. This
option is only applicable for paired-end reads.
-B Only count read pairs that have both ends aligned.
-P Check validity of paired-end distance when counting read pairs. Use -d and -D to
set thresholds.
-d <int>
Minimum fragment/template length, 50 by default.
-D <int>
Maximum fragment/template length, 600 by default.
-C Do not count read pairs that have their two ends mapping to different chromosomes
or mapping to same chromosome but on different strands.
--donotsort
Do not sort reads in BAM/SAM input. Note that reads from the same pair are required
to be located next to each other in the input.
# Number of CPU threads
-T <int>
Number of the threads. 1 by default.
# Read groups
--byReadGroup
Assign reads by read group. "RG" tag is required to be present in the input BAM/SAM
files.
# Long reads
-L Count long reads such as Nanopore and PacBio reads. Long read counting can only run
in one thread and only reads (not read-pairs) can be counted. There is no
limitation on the number of 'M' operations allowed in a CIGAR string in long read
counting.
# Miscellaneous
-R <format>
Output detailed assignment results for each read or readpair. Results are saved to
a file that is in one of the following formats: CORE, SAM and BAM. See Users Guide
for more info about these formats.
--tmpDir <string>
Directory under which intermediate files are saved (later removed). By default,
intermediate files will be saved to the directory specified in '-o' argument.
--maxMOp <int>
Maximum number of 'M' operations allowed in a CIGAR string. 10 by default. Both 'X'
and '=' are treated as 'M' and adjacent 'M' operations are merged in the CIGAR
string.
--verbose
Output verbose information for debugging, such as unmatched chromosome/contig
names.
-v Output version of the program.