Class
vcfc:VCFRecord
One tab-delimited VCF data line. It contains the eight mandatory fixed fields CHROM, POS, ID, REF, ALT, QUAL, FILTER, and INFO; it may additionally contain a FORMAT field and one value block per sample. This is a VCF-centric representation that can link to a sequence-alteration model via vcfc:asSequenceAlteration.
Outgoing Relationships
Edges emitted from this term while building the graph and reference views.
| Relation | Target | Target Description |
|---|---|---|
| Subclass Of |
prov:Entity
|
prov:Entity |
Incoming Relationships
Terms that point at this term in the generated relationship graph.
| Relation | Source | Source Description |
|---|---|---|
| Range |
vcfc:hasRecord
|
Associates a VCF file with one of its tab-delimited data records. |
| Domain |
vcfc:hasCall
|
Associates a VCF record with its vocabulary-level call resource, which groups QUAL, FILTER, INFO, FORMAT, and per-sample call data. |
| Domain |
vcfc:chromosome
|
Links a record to the declared contig corresponding to its CHROM value. The CHROM column identifies a reference sequence (or, for breakpoint assemblies, an angle-bracketed assembly contig ID); a resolvable external reference may also be aligned to FALDO. |
| Domain |
vcfc:chrom
|
The required CHROM fixed-field value: an identifier for the reference sequence on which the record is located, or an angle-bracketed assembly-contig ID for a breakpoint assembly. Records for one CHROM occur in a contiguous block. |
| Domain |
vcfc:pos
|
The required 1-based reference position of the record. It denotes the first base of REF, is numerically ordered within CHROM, and may be 0 or N+1 to indicate a telomere for a contig of length N. |
| Domain |
vcfc:recordId
|
The ID fixed-field value: a semicolon-separated list of unique record identifiers, such as dbSNP rs identifiers. When no identifier is available, VCF uses '.', represented here as '.'^^vcfc:Null. |
| Domain |
vcfc:ref
|
The required reference allele string. It contains one or more A, C, G, T, or N bases and begins at POS. For simple insertions, deletions, and symbolic alleles, VCF uses an adjacent padding base to avoid an empty allele. |
| Domain |
vcfc:alt
|
A lossless raw ALT lexical value. The VCF source serializes ALT as an ordered comma-separated list whose items may be base strings, '*', '.', symbolic IDs, '<*>', or breakend expressions. Repeated vcfc:alt assertions are unsuitable for per-allele annotation or preserving ALT order; use hasAltAllele and alleleIndex for the structural form. |
| Domain |
vcfc:recordIndex
|
record index |
| Domain |
vcfc:chromAssemblyContig
|
Associates a record whose CHROM is an angle-bracketed assembly-contig ID with that contig. It is the structured counterpart of vcfc:chromosome, which links a record to a declared reference contig; a record uses one or the other, never both. |
| Domain |
vcfc:hasIdentifier
|
has identifier |
| Domain |
vcfc:hasAltAllele
|
has alternate allele |
| Domain |
vcfc:hasReferenceAllele
|
has reference allele |
| Domain |
vcfc:hasPaddingInterpretation
|
Associates a record with the padding interpretation derived for its alleles. At most one interpretation is asserted per record. |
