.TH hifiasm 1 "19 July 2020" "hifiasm-0.9 (r289)" "Bioinformatics tools"

.SH NAME
.PP
hifiasm - haplotype-resolved de novo assembler for PacBio Hifi reads.

.SH SYNOPSIS

* Assemble HiFi reads:
.RS 4
.B hifiasm
.RB [ -o
.IR prefix ]
.RB [ -t
.IR nThreads ]
.RB [ -z
.IR endTrimLen ]
.R [options]
.I input1.fq
.RI [ input2.fq
.R [...]]
.RE

* Trio binning assembly with yak dumps:
.RS 4
.B yak count
.B -o
.I paternal.yak
.B -b37
.RB [ -t
.IR nThreads ]
.RB [ -k
.IR kmerLen ]
.I paternal.fq.gz
.br
.B yak count
.B -o
.I maternal.yak
.B -b37
.RB [ -t
.IR nThreads ]
.RB [ -k
.IR kmerLen ]
.I maternal.fq.gz
.br
.B hifiasm
.RB [ -o
.IR prefix ]
.RB [ -t
.IR nThreads ]
.R [options]
.B -1
.I paternal.yak
.B -2
.I maternal.yak
.I child.hifi.fq.gz
.RE

.SH DESCRIPTION
.PP
Hifiasm is an ultrafast haplotype-resolved de novo assembler for PacBio
Hifi reads. Unlike most existing assemblers, hifiasm starts from uncollapsed
genome. Thus, it is able to keep the haplotype information as much as possible.
The input of hifiasm is the PacBio Hifi reads in fasta/fastq format, and its
outputs consist of multiple types of assembly graph in GFA format.


.SH OPTIONS

.SS General options

.TP 10
.BI -o \ FILE
Prefix of output files [hifiasm.asm]. For detailed description of all assembly
graphs, please see the
.B OUTPUTS
section of this man-page. 

.TP 10
.BI -t \ INT
Number of CPU threads used by hifiasm [1]. 

.TP
.BI -h
Show help information.

.TP
.BI --version
Show version number. 


.SS Error correction options

.TP 10
.BI -k \ INT
K-mer length [51]. This option must be less than 64.

.TP
.BI -w \ INT
Minimizer window size [51].

.TP
.BI -f \ INT
Number of bits for bloom filter; 0 to disable [37]. This bloom filter is used
to filter out singleton k-mers when counting all k-mers. It takes
.RI 2^( INT -3)
bytes of memory. A proper setting saves memory. 37 is recommended for human
assembly.

.TP
.BI -r \ INT
Rounds of haplotype-aware error corrections [3]. This option affects all outputs of hifiasm.

.TP
.BI --min-hist-cnt \ INT
When analyzing the k-mer spectrum, ignore counts below
.IR INT .

.SS Assembly options

.TP
.BI -a \ INT
Rounds of assembly graph cleaning [4]. This option is used with
.B -x
and
.BR -y .
Note that unlike
.BR -r ,
this option does not affect error corrected reads and all-to-all overlaps.

.TP
.BI -z \ INT
Length of adapters that should be removed [0]. This option remove
.I INT
bases from both ends of each read.
Some old Hifi reads may consist of
short adapters (e.g., 20bp adapter at one end). For such data, trimming short adapters would 
significantly improve the assembly quality.

.TP
.BI -m \ INT
Maximal probing distance for bubble popping when generating primary/alternate
contig graphs [10000000]. Bubbles longer than
.I INT
bases will not be popped. For detailed description of these graphs, please see the
.B OUTPUTS
section of this man-page. 

.TP
.BI -p \ INT
Maximal probing distance for bubble popping when generating haplotype-resolved processed unitig graph
without small bubbles [100000]. Bubbles longer than
.I INT
bases will not be popped. Small bubbles might be caused by somatic mutations or noise in data, which
are not the real haplotype information. For detailed description of this graph, please see the
.B OUTPUTS
section of this man-page. 

.TP
.BI -n \ INT
A unitig is considered small if it is composed of less than 
.I INT
reads [3]. Hifiasm may try to remove small unitigs at various steps.

.TP
.BI -x \ FLOAT, -y \ FLOAT
Max and min overlap drop ratio [0.8, 0.2]. This option is used with
.BR -r .
Given a node
.I N
in the assembly graph, let max(N)
be the length of the largest overlap of
.I N.
Hifiasm iteratively drops overlaps of
.I N
if their length / max(N)
are below a threshold controlled by
.B -x
and
.BR -y .
Hifiasm applies
.B -r
rounds of short overlap removal with an increasing threshold between
.B -x
and
.BR -y .

.TP
.BI -i
Ignore error corrected reads and overlaps saved in
.IR prefix .*.bin
files.
Apart from assembly graphs, hifiasm also outputs three binary files
that save all overlap information during assembly step.
With these files, hifiasm can avoid the time-consuming all-to-all overlap calculation step,
and do the assembly directly and quickly.
This might be helpful when users want to get an optimized assembly by multiple rounds of experiments
with different parameters.

.TP
.BI --pri-range \ INT1[,INT2]
Min and max coverage cutoff of primary contigs.
Keep contigs with coverage in this range at p_ctg.gfa. 
Inferred automatically in default.
If INT2 is not specified, it is set to infinity. 
Set -1 to disable.

.TP
.BI --lowQ \ INT
Output contig regions with >=INT% inconsistency to the bed file 
with suffix
.B lowQ.bed
[70]. Set 0 to disable. 

.SS Trio-partition options

.TP 10
.BI -1 \ FILE
K-mer dump generated by
.B yak count
from the paternal/haplotype1 reads []

.TP
.BI -2 \ FILE
K-mer dump generated by
.B yak count
from the maternal/haplotype2 reads []

.TP
.BI -3 \ FILE
List of paternal/haplotype1 read names []

.TP
.BI -4 \ FILE
List of maternal/haplotype2 read names []

.TP
.BI -c \ INT
Lower bound of the binned k-mer's frequency [2]. When doing trio binning, 
a k-mer is said to be differentiating if it occurs >=
.B -d
times in one sample 
but occurs <
.B -c
times in the other sample.

.TP
.BI -d \ INT
Upper bound of the binned k-mer's frequency [5]. When doing trio binning, 
a k-mer is said to be differentiating if it occurs >=
.B -d
times in one sample 
but occurs <
.B -c
times in the other sample.


.SS Purge-dups options

.TP 10
.BI -l \ INT
Level of purge-dup. 0 to disable purge-dup, 1 to only purge contained haplotigs, 
2 to purge all types of haplotigs. In default, [2] for non-trio assembly, [0] for trio assembly.
For trio assembly, only level 0 and level 1 are allowed.

.TP
.BI -s \ FLOAT
Similarity threshold for duplicate haplotigs that should be purged [0.75].

.TP
.BI -O \ FLOAT
Min number of overlapped reads for duplicate haplotigs that should be purged [1].

.TP
.BI --purge-cov \ INT
Coverage upper bound of Purge-dups, which is inferred automatically in default.
If the coverage of a contig is higher than this bound, don't apply Purge-dups.

.TP
.BI --high-het \ INT
Enable this mode for high heterozygosity sample, which will increase running time. 
For ordinary samples, no need to enable this mode [experimental, not stable].


.SS Debugging options

.TP 10
.B --dbg-gfa
Write additional files to speed up the debugging of graph cleaning.


.SH OUTPUTS

.PP
Without trio partition options
.B -1
and
.BR -2 ,
hifiasm generates the following assembly graphs in the GFA format:

.RS 2
.TP 2
*
.IR prefix .r_utg.gfa:
haplotype-resolved raw unitig graph. This graph keeps all haplotype information.

.TP
*
.IR prefix .p_utg.gfa:
haplotype-resolved processed unitig graph without small bubbles.  Small bubbles
might be caused by somatic mutations or noise in data, which are not the real
haplotype information.  The size of popped small bubbles should be specified by
.BR -p .

.TP
*
.IR prefix .p_ctg.gfa:
assembly graph of primary contigs. This graph collapses different haplotypes.

.TP
*
.IR prefix .a_ctg.gfa:
assembly graph of alternate contigs. This graph consists of all assemblies that
are discarded in primary contig graph.

.RE

.PP
With trio partition, hifiasm outputs the following assembly graphs:

.RS 2
.TP 2
*
.IR prefix .dip.r_utg.gfa:
haplotype-resolved raw unitig graph. This graph keeps all haplotype information.

.TP
*
.IR prefix .hap1.p_ctg.gfa:
phased paternal/haplotype1 contig graph. This graph keeps the phased
paternal/haplotype1 assembly.

.TP
*
.IR prefix .hap2.p_ctg.gfa:
phased maternal/haplotype2 contig graph. This graph keeps the phased
maternal/haplotype2 assembly.
.RE

.PP
For each graph, hifiasm also outputs a simplified version without sequences for
the ease of visualization. Hifiasm keeps corrected reads and overlaps in three
binary files such as it can regenerate assembly graphs from the binary files
without redoing error correction.