LICENSE

Licensed under the Apache License, Version 2.0 (the "License"); you may not use this file except in compliance with the License. You may obtain a copy of the License at

http://www.apache.org/licenses/LICENSE-2.0

Unless required by applicable law or agreed to in writing, software distributed under the License is distributed on an "AS IS" BASIS, WITHOUT WARRANTIES OR CONDITIONS OF ANY KIND, either express or implied. See the License for the specific language governing permissions and limitations under the License.

AUTHORS

Rishi Nag <rishi@ebi.ac.uk>, original author.

Alessandro Vullo <avullo at cpan.org>, the current developer and maintainer.

NAME

Bio::DB::HTS::VCF -- Read VCF/BCF data files

DESCRIPTION

This module provides a Perl interface to the HTSlib library for reading variant calls stored in VCF and BCF file databases.

The functions provided are for opening a VCF/BCF file, reading header values, querying specific chromosome intervals and then reading row values.

A sweep set of methods allows running through rows one by one, either backwards or forwards through the file.

SYNOPSIS

use Bio::DB::HTS::VCF ;

### File Open ###
my $v = Bio::DB::HTS::VCF->new( filename => "/path/to/myfile.vcf.gz" );

# once the file has been opened, various global values can be read from the header
my $h = $v->header();

$h->get_seqnames() ;
$h->version() ;  # read the VCF file version

$h->num_samples() ;
$h->get_sample_names() ; #return an array of sample names

$h->num_seqnames() ;
$h->get_seqnames() ; # return an array of sequence names

### Individual rows can be read in and fields accessed ###
my $row = $v->next() ;

# row functions
$row->chromosome($h) ;
$row->position() ;
$row->id() ;
$row->num_filters() ;
$row->quality() ;

# retrieve alleles
my $num_alleles = $row->num_alleles();
my $alleles = $row->get_alleles();
my $allele_index = 1;
for my $a (@$alleles) {
  printf( "(%s, %s)\n", $a, $row->get_variant_type($allele_index++) ) ;
}

# query filters
$row->has_filter($h,"DP50");
$row->has_filter($h,"."); # PASS filter check

$row->get_info_type($h, "AF"); # one of "String", "Integer", "Float" or "Flag".
$info_result = $row->get_info($h, "NS"); # [3]

$row->get_format_type($h, "GT") ; # "String"
$row->get_format($h, "DP") ; # [ 1, 8, 5 ]

### free memory associated with the row
Bio::DB::HTS::VCF::Row->destroy($row);

### query specific locations
my $iter = $v->query("20:1000000-1231000");
while (my $result = $iter->next) {
  print $result->chromosome($h), $result->position(), $result->id(), $result->num_filters(), $result->quality(), "\n";
}

METHODS

`new`

Opens a VCF/BCF file for reading. If the file is indexed (i.e. tabix for VCF, csi for BCF) the index is opened and used for querying arbitrary locations on the chromosomes.

$vcf = Bio::DB::HTS::VCF->new($filepath): Returns an instance of Bio::DB::HTS::VCF.

`header`

Returns instance of Bio::DB::HTS::VCF::Header, representing the header of the file.

$header = $vcf->header()

`num_variants`

Returns the number of variants (i.e. rows) of the file.

$nv = $vcf->num_variants();

`close`

Close the VCF/BCF file, allocated memory will be released, included the index, if present.

$vcf->close()

`next`

Returns the next row (starting from the first one) read from the file.

$row = $vcf->next(): Returns an instance of Bio::DB::HTS::VCF::Row or undef if end of file is reached.

Querying an indexed VCF/BCF file

If the file is indexed, the file can be queried for variants on a specified region. Regions can be specified using either the "chr", "chr:start" or "chr:start-end" format, with start <= end.

Once an iterator is obtained, individual rows belonging to the result set can be sequentially accessed by iteratively invoking the iterator next method until it returns nothing.

`query`

$iterator = $vcf->query($region);: Returns an instance of Bio::DB::HTS::VCF::Iterator or undef if the chromosome is not found in the index or raises an exception in case the underlying HTSlib library cannot parse the region.

HEADER METHODS

Once the file has been opened, various global values can be read from the header.

`version`

Returns the VCF file version, as a string

$h->version()

`num_samples`

Returns the number of samples

$h->num_samples()

`get_sample_names`

Returns the list of sample names

$sample_names = $h->get_sample_names(): Returns an array ref of strings representing the sample names

`get_seqnames`

Returns the number of sequence names

$h->num_seqnames()

`get_seqnames`

Returns the list of sequence names

$h->get_seqnames(): Returns an array ref of strings representing the sequence names

`fmt_text`

Get header formatted text, as a string

$h->fmt_text(): Returns the text string representing the content of the header

ROW METHODS

Individual rows can be read in and fields accessed. To read a row use the next function, which returns a Bio::DB::HTS::VCF::Row instance.

Various fields can then be read from the row object. Some of the functions to read these fields will need the header object supplied.

$row->print($header): Returns a formatted textual representation of the row.
$row->chromosome($header)
$row->position()
$row->id()
$row->quality()
$row->reference()

Accessing alleles information

$row->num_alleles(): Returns the number of alleles
$row->get_alleles(): Returns the alleles as strings in an array ref

The variant type of an allele can be determined using the index of the allele. The index starts from 1 for the first allele:

$row->is_snp()

Returns a true value if the row refers to a SNP.

$row->get_variant_type($allele_index)

This will return one of the values as defined in htslib. As of v1.3.1 these are as follows.

VCF_REF 0
VCF_SNP 1
VCF_MNP 2
VCF_INDEL 4
VCF_OTHER 8

Row filters

Each row object has filters that may or may not have been applied to it.

$row->num_filters(): Returns the number of filters of the row.
$row->has_filter($header, $filter): Returns 0 if the filter is not present, 1 if it is present. The PASS filter is represented by a dot.

Accessing info fields

Each row may have additional info fields associated with each allele in the row.

$row->get_info_type($header, $info_id)

Returns the type of the info ID as specified in the VCF file header, one of "String", "Integer", "Float" or "Flag".

$row->get_info($header, $info_id) or $row->get_info($header)

If an info_id string is passed, returns an array ref of values for that particular info field, one for each allele in the row. If the row does not have an item of that info, or it does not exist in the file, a string "ID_NOT_FOUND" will be returned.

Alternatively, the get_info() method can be invoked by just passing the header. In this case, the whole info field is returned organised as a hash ref where keys are the info IDs and values are the info fields for the corresponding ID.

Accessing format fields

Formats are dealt with similarly to info fields.

$row->get_format_type($header, $format_id)

Returns the type of the format ID as specified in the VCF file header, one of "String", "Integer", "Float" or "Flag".

$row->get_format($header, $format_id) or $row->get_format($header)

If a format_id string is passed, returns an array ref of values for that particular format ID. If the row does not have an item of that format, or it does not exist in the file, a string "ID_NOT_FOUND" will be returned.

Alternatively, the get_format() method can be invoked by just passing the header. In this case, it returns the complete format specification as a hash ref of FORMAT_ID => [ FORMAT_ID_VALUE, ... ].

Accessing genotypes

Genotype records are currently returned as a series of integers, across all the samples for the row.

$row->get_genotypes($header): Returns an array reference of integers representing genotype records.

VCF SWEEP OBJECTS

Open the file and process using sweeps. Note that the two methods maintain pointers that are independant of one another. Using the next_row() will start at the first row in the file and go on to the next row in subsequent reads. This is independant of previous_row() calls. Similarly previous_row() will start at the last row and read backwards. However a call to next_row() is needed beforehand as the read fails otherwise.

At the time of writing there are issues which seem to be due to the underlying HTSlib API calls, so using the next() function is preferable to using sweeps.

use Bio::DB::HTS::VCF ;

my $sweep = Bio::DB::HTS::VCFSweep->new(filename => "data/test.vcf.gz");
$sweep->header;
my $row_forwards = $sweep->next_row(); #returns first row in file
my $row_backwards = $sweep->previous_row(); #returns last row in file
my $row_forwards = $sweep->next_row(); # returns second row in file
my $row_backwards = $sweep->previous_row(); #returns penultimate row in file

To install Bio::DB::HTS, copy and paste the appropriate command in to your terminal.

cpanm

cpanm Bio::DB::HTS

CPAN shell

perl -MCPAN -e shell
install Bio::DB::HTS

For more information on module installation, please visit the detailed CPAN module installation guide.

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LICENSE

AUTHORS

NAME

DESCRIPTION

SYNOPSIS

METHODS

new

header

num_variants

close

next

Querying an indexed VCF/BCF file

query

HEADER METHODS

version

num_samples

get_sample_names

get_seqnames

get_seqnames

fmt_text

ROW METHODS

Accessing alleles information

Row filters

Accessing info fields

Accessing format fields

Accessing genotypes

VCF SWEEP OBJECTS

Module Install Instructions

`new`

`header`

`num_variants`

`close`

`next`

`query`

`version`

`num_samples`

`get_sample_names`

`get_seqnames`

`get_seqnames`

`fmt_text`