A collection of scripts useful for working with PacBio-based assemblies.
The pacbio-util script requires BioPerl and samtools >= 0.1.19.
We have noticed that PacBio assemblies can show single-base deletions, in most cases, in proximity to even fairly short homopolymer runs. This does not occur at all homopolymer runs, and in our limited samples incidence rate is perhaps 1 in 10kbp. Single-base insertions and longer insertions may occur but are much rarer.
There are three steps to applying this correction. First, map a set of Illumina reads to the PacBio assembly to generate sorted BAM file(s). Reads from multiple BAMs will be combined. These reads should be from the same individual/strain from which the assembly was created. Reads from other sequencing technologies, or from another individual/strain, will reduce the effectiveness of the correction and may introduce further errors. In all subsequent steps it is required that the order of the sequences in the assembly and the BAMs is identical.
Second, use the pacbio-util script here to generate a set of indel targets
for correction. The command is pacbio-util indel-targets, and the criteria
for determining targets may be modified via options. Use the -h option to
see available options and current defaults.
The third and final step is to use the command pacbio-util indel-apply to
apply the targets generated in the second step to the assembly to create a
corrected assembly. Options may also be used here to restrict the set of
targets applied; use the -h option to see available options and current
defaults.
For an assembly pacbio_assembly.fasta, and mappings of Illumina paired-end
and single-end reads to this assembly in BAM files pe.sorted.bam and
se.sorted.bam, the following will generated the list of indel targets to
targets.txt and a corrected assembly to corrected_assembly.fasta.
pacbio-util indel-targets -f pacbio_assembly.fasta pe.sorted.bam se.sorted.bam > targets.txt
pacbio-util indel-apply -f pacbio_assembly.fasta -t targets.txt > corrected_assembly.fastaThe indel-apply command can find the assembly used for determining the
targets by using the first line of the list of targets. This provides a useful
shortcut for combining both commands into a one-line piped command. The tee
is in place to save the list of targets as they pass through to indel-apply.
pacbio-util indel-targets -f pacbio_assembly.fasta pe.sorted.bam se.sorted.bam \
| tee targets.txt \
| pacbio-util indel-apply > corrected_assembly.fastaHere is example tool output (with -v) and scaffold size results before and
after correction.
$ pacbio-util indel-targets -v -f pacbio_assembly.fasta pe.sorted.bam se.sorted.bam | tee targets.txt | pacbio-util indel-apply -v > corrected_assembly.fasta
samtools pipe command: 'samtools mpileup -s -B -d 10000 -L 10000 --ff 1280 -q 1 -Q 13 -f pacbio_assembly.fasta pe.sorted.bam se.sorted.bam |'
[mpileup] 2 samples in 2 input files
Merging columns from 2 BAM files ...
pacbio-util indel-targets: 1281 targets generated for assembly pacbio_assembly.fasta
pacbio-util indel-apply: Opening target assembly 'pacbio_assembly.fasta'
pacbio-util indel-apply: unitig_7, no targets
pacbio-util indel-apply: unitig_52, no targets
pacbio-util indel-apply: unitig_46, no targets
pacbio-util indel-apply: unitig_14, no targets
pacbio-util indel-apply: unitig_54, no targets
pacbio-util indel-apply: unitig_44, no targets
pacbio-util indel-apply: unitig_13, no targets
pacbio-util indel-apply: unitig_56, no targets
pacbio-util indel-apply: unitig_55, no targets
pacbio-util indel-apply: unitig_43, no targets
pacbio-util indel-apply: unitig_48, no targets
pacbio-util indel-apply: unitig_45, no targets
pacbio-util indel-apply: unitig_15, no targets
pacbio-util indel-apply: unitig_47, no targets
pacbio-util indel-apply: unitig_60, no targets
pacbio-util indel-apply: unitig_61, no targets
pacbio-util indel-apply: unitig_51, no targets
pacbio-util indel-apply: unitig_59, no targets
pacbio-util indel-apply: unitig_4, no targets
pacbio-util indel-apply: 1281 targets applied to assembly pacbio_assembly.fasta
$
| Scaffold | bp before | bp after |
|---|---|---|
| unitig_1 | 6250549 | 6250752 |
| unitig_10 | 1811588 | 1811655 |
| unitig_7 | 15299 | 15299 |
| unitig_52 | 7932 | 7932 |
| unitig_46 | 8606 | 8606 |
| unitig_14 | 1884 | 1884 |
| unitig_0 | 10120325 | 10120600 |
| unitig_8 | 3934972 | 3935082 |
| unitig_12 | 240123 | 240143 |
| unitig_3 | 16252 | 16253 |
| unitig_54 | 22065 | 22065 |
| unitig_44 | 12520 | 12520 |
| unitig_53 | 5951772 | 5951911 |
| unitig_13 | 86224 | 86224 |
| unitig_56 | 30475 | 30475 |
| unitig_55 | 15275 | 15275 |
| unitig_41 | 19231 | 19232 |
| unitig_43 | 9344 | 9344 |
| unitig_58 | 6608738 | 6608943 |
| unitig_9 | 2363594 | 2363680 |
| unitig_48 | 30325 | 30325 |
| unitig_45 | 14763 | 14763 |
| unitig_57 | 18691 | 18685 |
| unitig_15 | 2004 | 2004 |
| unitig_47 | 15558 | 15558 |
| unitig_6 | 4486498 | 4486633 |
| unitig_60 | 26006 | 26006 |
| unitig_61 | 16086 | 16086 |
| unitig_51 | 9410 | 9410 |
| unitig_59 | 14740 | 14740 |
| unitig_4 | 19898 | 19898 |
Generate indel targets for correction. Uses samtools mpileup for
indel detection. Targets are written to standard output.
Targets will only be generated where all read mappings containing an indel agree on the size and sequence of the indel. Further criteria for minimum indel fraction, minimum coverage, and maximum indel size may be adjusted via options.
pacbio-util indel-targets -f FASTA FILE1.bam [ FILE2.bam ... ]
OPTIONS
-f FILE, --fasta FILE PacBio assembly in Fasta format
FILE1.bam [ FILE2.bam ] BAM files of reads mapped to
- Read mpileup from stdin rather than running
samtools. Note that mapping qualities
(option `-s`) are expected in the mpileup input.
--indel-frac FLOAT Do not report indels at a position if the
fraction of reads containing them is below FLOAT
[default 0.8]
--indel-min-cov INT Minimum read coverage to consider an indel
[default 10]
--include-bad-indels Include indels in target set that do not pass
our criteria, these lines are marked 'bad' in
the sixth column
--max-indel-size INT Maximum indel size to accept, beyond this the
position is considered in error [default 1000]
--mapping-quality FLOAT Minimum mean mapping quality of reads covering a
target site. Note that a value of 0 means no
minimum applied; reads with 0 mapQ are still
excluded by default (see --all-reads) [default 0]
--all-reads Include all reads. Default is to exclude
multiply-mapped reads (mapQ < 1), alignments
that are not the primary (SAM flag 256), and
duplicate alignments (flag 1024).
--all-bases Include all bases. Default is to exclude bases
below quality 13.
--samtools FILE Location of samtools executable
[default samtools]
--verbose Print informational messages
--help, -? help message
Below is an example subset of targets generated with this command. The first
line of the targets output is the name of the assembly Fasta file against which
the targets were generated. Following that, the columns are scaffold name,
target position, reference base, total read coverage, type of target (always
indel for this command), whether the target passed quality criteria (good
or bad), the frequency of coverage supporting the indel, the size of the
indel (positive for insertion, negative for deletion), a string describing the
indel size and sequence, the number of reads supporting the indel, and the mean
mapping quality of reads.
#assembly:pacbio_assembly.fasta
unitig_1 101522 C 72 indel good 0.9444 1 +1A 68 60
unitig_1 119319 G 127 indel good 0.8110 1 +1A 103 60
unitig_1 120891 A 104 indel good 0.9231 1 +1T 96 60
unitig_1 122801 A 93 indel good 0.9032 1 +1C 84 60
unitig_1 125303 G 84 indel good 0.9286 1 +1A 78 60
unitig_1 131734 T 67 indel good 0.8657 1 +1A 58 60
unitig_1 136434 A 28 indel good 0.8214 1 +1C 23 60
unitig_1 170949 A 40 indel good 0.9500 1 +1G 38 60
unitig_1 171182 A 80 indel good 0.9500 1 +1G 76 60
unitig_1 172016 A 67 indel good 0.9403 1 +1C 63 60
unitig_1 190068 A 18 indel good 1.0000 1 +1G 18 60
unitig_1 190154 T 11 indel good 0.9091 1 +1G 10 60
unitig_1 191027 C 104 indel good 0.9231 1 +1G 96 60
unitig_1 191173 C 96 indel good 0.9167 1 +1T 88 60
unitig_1 230981 T 63 indel good 0.9683 1 +1C 61 60
unitig_1 270949 G 100 indel good 0.9800 1 +1C 98 60
unitig_1 307836 A 38 indel good 0.8947 1 +1C 34 60
unitig_1 310152 C 105 indel good 0.8857 1 +1A 93 60
unitig_1 326536 G 105 indel good 0.9143 1 +1A 96 60
unitig_1 360786 G 39 indel good 0.8205 1 +1A 32 58.5
unitig_1 369367 C 98 indel good 0.9592 1 +1A 94 60
unitig_1 371657 T 48 indel good 0.9375 1 +1G 45 60
unitig_1 371776 G 43 indel good 1.0000 1 +1T 43 60
unitig_1 373159 C 113 indel good 0.9469 1 +1A 107 60
Apply indel targets to correct an assembly. The corrected assembly is written to standard output. The order of sequences in the assembly must be the same as that in the targets.
pacbio-util indel-apply [ -f FASTA ] [ -t TARGETS ]
OPTIONS
-f | --fasta FILE PacBio assembly in Fasta format, to be corrected.
Must be the same assembly used for
'./pacbio-util indel-targets'.
If the assembly is not specified, it is determined
from the first line of the target list.
-t | --targets TARGETS List of indel targets to apply, standard output
from './pacbio-util indel-targets -f FILE ...'. If no
targets are specified, they are read from stdin.
--include-bad-indels Apply indels in target set that are marked 'bad'
--max-indel-size INT Maximum indel size to apply [default 1000]
--min-indel-frac FLOAT Minimim indel fraction to apply, a value of 0
means apply all indels in target set [default 0]
--skip-deletion-verify Do not verify that a deletion matches the
sequence at that position in the assembly
[default 0]
--skip-softmasked Do not apply targets to softmasked regions of the
assembly, as determined by use of lowercase
[default 0]
--verbose Print informational messages
--help, -? help message
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