variant-extractor 4.0.6

Deterministic and standard extractor of indels, SNVs and structural variants (SVs) from VCF files

VariantExtractor

Deterministic and standard extractor of indels, SNVs and structural variants (SVs) from VCF files built under the frame of EUCANCan's second work package. VariantExtractor is a Python package (requires Python version 3.6 or higher) and provides a set of data structures and functions to extract variants from VCF files in a deterministic and standard way while adding information to facilitate afterwards processing. It homogenizes multiallelic variants, MNPs and SVs (including imprecise paired breakends and single breakends). The package is designed to be used in a pipeline, where the variants are ingested from VCF files and then used in downstream analysis. Check the available documentation for more information.

While there is somewhat of an agreement on how to label the SNVs and indels variants, this is not the case for the structural variants. In the current scenario, different labeling between variant callers makes comparisons between structural variants difficult. This package provides an unified interface to extract variants (included structural variants) from VCFs generated by different variant callers. Apart from reading the VCF file, VariantExtractor adds a preprocessing layer to homogenize the variants extracted from the file. This way, the variants can be used in downstream analysis in a consistent way. For more information about the homogenization process, check the homogenization rules section.

Table of contents

• Getting started
  • Installation
• Usage
• VariantRecord
  • VariantType
  • BreakendSVRecord
  • ShorthandSVRecord
• Homogenization rules
  • Multiallelic variants
  • SNVs
  • Structural variants
    • Breakend vs shorthand notation
    • Paired breakends
    • Inferred breakend pairs
    • Imprecise paired breakends
    • Single breakends
• Dependencies

Getting started

Installation

VariantExtractor is available on PyPI and can be installed using pip:

pip install variant-extractor

Usage

# Import the package
from variant_extractor import VariantExtractor

# Create a new instance of the class
extractor = VariantExtractor('/path/to/file.vcf')
# Iterate through the variants
for variant_record in extractor:
    print(f'Found variant of type {variant_record.variant_type.name}: {variant_record.contig}:{variant_record.pos}')

# Import the package
from variant_extractor import VariantExtractor

# Create a new instance of the class
extractor = VariantExtractor('/path/to/file.vcf')

# Save variants to a CSV file
extractor.to_dataframe().drop(['variant_record_obj'], axis=1).to_csv('/path/to/output.csv', index=False)

For a more complete list of examples, check the examples directory. This folder also includes an example of a script for normalizing VCF files following the homogenization rules.

VariantRecord

The VariantExtractor constructor returns a generator of VariantRecord instances. The VariantRecord class is a container for the information contained in a VCF record plus some extra useful information.

Property	Type	Description
contig	str	Contig name
pos	int	Position on the contig
end	int	End position of the variant in the contig (same as pos for TRN and SNV)
length	int	Length of the variant
id	Optional[str]	Record identifier
ref	str	Reference sequence
alt	str	Alternative sequence
qual	Optional[float]	Quality score for the assertion made in ALT
filter	List[str]	Filter status. PASS if this position has passed all filters. Otherwise, it contains the filters that failed
info	Dict[str, Any]	Additional information
format	List[str]	Specifies data types and order of the genotype information
samples	Dict[str, Dict[str, Any]]	Genotype information for each sample
variant_type	VariantType	Variant type inferred
alt_sv_breakend	Optional[BreakendSVRecord]	Breakend SV info, present only for SVs with breakend notation. For example, G]17:198982]
alt_sv_shorthand	Optional[ShorthandSVRecord]	Shorthand SV info, present only for SVs with shorthand notation. For example, <DUP:TANDEM>

VariantType

The VariantType enum describes the type of the variant. For structural variants, it is inferred only from the breakend notation (or shorthand notation). It does not take into account any INFO field (SVTYPE nor EVENTYPE) that might be added by the variant caller afterwards.

REF	ALT	Variant name	Description
A	G	SNV	Single nucleotide variant
AGTG	A	DEL	Deletion
A	A[1:20[ or <DEL>	DEL	Deletion
A	ACCT or <INS>	INS	Insertion
A	]1:20]A or <DUP>	DUP	Duplication
A	A]1:20] or [1:20[A	INV	Inversion. <INV> is a special case
A	<CNV>	CNV	Copy number variation
A	A]X:20] or A[X:20[ or ]X:20]A or [X:20[A	TRN	Translocation
A	A. or .A	SGL	Single breakend

BreakendSVRecord

The BreakendSVRecord class is a container for the information contained in a VCF record for SVs with breakend notation.

Property	Type	Description
prefix	Optional[str]	Prefix of the SV record with breakend notation. For example, for G]17:198982] the prefix will be G
bracket	str	Bracket of the SV record with breakend notation. For example, for G]17:198982] the bracket will be ]
contig	str	Contig of the SV record with breakend notation. For example, for G]17:198982] the contig will be 17
pos	int	Position of the SV record with breakend notation. For example, for G]17:198982] the position will be 198982
suffix	Optional[str]	Suffix of the SV record with breakend notation. For example, for G]17:198982] the suffix will be None

ShorthandSVRecord

The ShorthandSVRecord class is a container for the information contained in a VCF record for SVs with shorthand notation.

Property	Type	Description
type	str	Type of the SV record with shorthand notation. One of the following, 'DEL', 'INS', 'DUP', 'INV' or 'CNV'. For example, for <DUP:TANDEM> the type will be DUP
extra	List[str]	Extra information of the SV. For example, for <DUP:TANDEM:AA> the extra will be ['TANDEM', 'AA']

Homogenization rules

VariantExtractor provides a unified interface to extract variants (included structural variants) from VCF files generated by different variant callers. The variants are homogenized and returned applying the following rules:

Multiallelic variants

An entry with multiple ALT sequences (multiallelic) is divided into multiple entries with a single ALT field. This entries with a single ALT field are then processed with the rest of the homogeneization rules. For example:

CHROM	POS	ID	REF	ALT	FILTER
2	1	multiallelic_1	G	C,T	PASS

is returned as:

CHROM	POS	ID	REF	ALT	FILTER	VariantType
2	1	multiallelic_1_0	G	C	PASS	SNV
2	1	multiallelic_1_1	G	T	PASS	SNV

SNVs

Entries with REF/ALT of the same lenghts are treated like SNVs. If the REF/ALT sequences are more than one nucleotide (MNPs), they are divided into multiple atomic SNVs. For example:

CHROM	POS	ID	REF	ALT	FILTER
2	1	snv_1	C	G	PASS
2	3	mnp_1	TAG	AGT	PASS

are returned as:

CHROM	POS	ID	REF	ALT	FILTER	VariantType
2	3	snv_1	C	G	PASS	SNV
2	3	mnp_1_0	T	A	PASS	SNV
2	4	mnp_1_1	A	G	PASS	SNV
2	5	mnp_1_2	G	T	PASS	SNV

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Structural variants

VariantExtractor returns one entry per structural variant (one entry per breakend pair). This helps to avoid the ambiguity of the notation and keeps the process deterministic. For this reason, in case of paired breakends, the breakend with the lowest chromosome and/or position is returned. If a breakend is not the lowest chromosome and/or position and is missing its pair, its pair is inferred and returned.

Breakend vs shorthand notation

Entries with the same information, either described with shorthand or breakend notation, will be returned the same way. Here is an example for a DEL entry:

CHROM	POS	ID	REF	ALT	FILTER	INFO
1	3000	event_1_o	A	A[1:5000[	PASS	SVTYPE=BND
1	5000	event_1_h	A	]1:3000]A	PASS	SVTYPE=BND
1	3000	event_1	A	A[1:5000[	PASS	SVTYPE=DEL
1	3000	event_1	A	<DEL>	PASS	SVTYPE=DEL; END=5000
1	3000	event_1	AGTCACAA...	A	PASS

are returned as one entry (each one of them with their own ALT field), but with the same VariantRecord.end and VariantType:

CHROM	POS	ID	REF	ALT	FILTER	INFO	VariantType	VariantRecord.end
1	3000	event_1	A	...	PASS	...	DEL	5000

The special case of INV

<INV> is a special case of shorthand notation because it represents two paired breakends. For example, the following shorthand notation:

CHROM	POS	ID	REF	ALT	FILTER	INFO
2	321682	event_1	T	<INV>	PASS	SVTYPE=INV;END=421681

is equivalent to the following breakends:

CHROM	POS	ID	REF	ALT	FILTER	INFO	VariantType
2	321681	event_1_0	N	N]2:421681]	PASS	SVTYPE=INV	INV
2	321682	event_1_1	T	[2:421682[T	PASS	SVTYPE=INV	INV

In this case, VariantExtractor converts internally <INV> to two entries with breakend notation (one for each breakend pair). Note that the N will be replaced with the correct nucleotide if fasta_ref is provided to VariantExtractor.

Paired breakends

For paired breakends, breakends are paired using the INFO fields MATEID or PARID. If these fields are not available, they are paired using their coordinates (contig+position). The breakend with the lowest chromosome and/or position is returned. For example:

CHROM	POS	ID	REF	ALT	FILTER	INFO
2	3000	event_1_o	T	]3:5000]T	PASS	SVTYPE=BND
3	5000	event_1_h	G	G[2:3000[	PASS	SVTYPE=BND
1	3000	event_2_o	A	A[1:5000[	PASS	SVTYPE=BND
1	5000	event_2_h	A	]1:3000]A	PASS	SVTYPE=BND

are returned as one entry per variant:

CHROM	POS	ID	REF	ALT	FILTER	INFO	VariantType
2	3000	event_1_o	T	]3:5000]T	PASS	SVTYPE=BND	TRN
1	3000	event_2_o	A	A[1:5000[	PASS	SVTYPE=BND	DEL

Inferred breakend pairs

If all breakends are missing their pair, the breakends with the lowest chromosome and/or position are inferred and returned. For example:

CHROM	POS	ID	REF	ALT	FILTER	INFO
3	5000	event_1_h	G	G[2:3000[	PASS	SVTYPE=BND
1	5000	event_2_h	A	]1:3000]A	PASS	SVTYPE=BND

are returned as their inferred breakend pair with the lowest chromosome and/or position:

CHROM	POS	ID	REF	ALT	FILTER	INFO	VariantType
2	3000	event_1_h	N	]3:5000]N	PASS	SVTYPE=BND	TRN
1	3000	event_2_h	A	A[1:5000[	PASS	SVTYPE=BND	DEL

Note that the N will be replaced with the correct nucleotide if fasta_ref is provided to VariantExtractor. The following equivalencies are applied:

CHROM1	POS1	REF1	ALT1	CHROM2	POS2	REF2	ALT2
1	500	N	N[7:800[	7	800	N	]1:500]N
1	500	N	]7:800]N	7	800	N	N[1:500[
1	500	N	[7:800[N	7	800	N	[1:500[N
1	500	N	N]7:800]	7	800	N	N]1:500]

Imprecise paired breakends

Imprecise breakends do not match exactly with their pair in coordinates. In this case, they are paired using the INFO fields MATEID or PARID. As with the rest of variants, for each breakend pair, only the breakend with the lowest chromosome and/or position is returned. However, it is important to notice that the CIPOS field is lost for the other breakend. For example:

CHROM	POS	ID	REF	ALT	FILTER	INFO
2	3010	event_1_o	T	T[3:5000[	PASS	SVTYPE=BND;CIPOS=0,50;PARID=event_1_h
3	5050	event_1_h	A	]2:3050]A	PASS	SVTYPE=BND;CIPOS=0,100;PARID=event_1_o

are paired and the entry with the lowest chromosome and/or position is returned:

CHROM	POS	ID	REF	ALT	FILTER	INFO	VariantType
2	3010	event_1_o	T	T[3:5000[	PASS	SVTYPE=BND;CIPOS=0,50;PARID=a_h	TRN

Single breakends

Single breakends cannot be matched with other breakends because they lack a mate. They may be able to be matched later in downstream analysis. That is why each one is kept as a different variant. For example:

CHROM	POS	ID	REF	ALT	FILTER	INFO
2	3000	event_s	T	T.	PASS	SVTYPE=BND
3	5000	event_m	G	.G	PASS	SVTYPE=BND

are returned as two entries:

CHROM	POS	ID	REF	ALT	FILTER	INFO	VariantType
2	3000	event_s	T	T.	PASS	SVTYPE=BND	SGL
3	5000	event_m	G	.G	PASS	SVTYPE=BND	SGL

Dependencies

The dependencies are covered by their own respective licenses as follows:

• Python/Pysam package (MIT license)