GFF3 features (C. briggsae)
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Jump to navigationJump to searchThis article describes features included in the C. briggsae GFF3 files. For introduction information on the GFF3 files, please see [[GFF3_features GFF3 features] article.
The WormBase C. briggsae GFF3 files can be downloaded from:
ftp://ftp.wormbase.org/pub/wormbase/genomes/briggsae/genome_feature_tables/GFF3
The attribute tags (column 9) for each feature group are listed in parenthesis. Some attributes listed for a feature group may not be available for each feature within the group.
FEATURES
- The source field for coding gene features is "Coding_transcript". CDS, mRNA, exon and introns are available.
CDS:Coding_transcript (ID,Note,brigpep,ortholog,predicted_once,supported_by_multiple_predictions, supported_by_ortholog,supported_by_paralogs) mRNA:Coding_transcript (ID) exon:Coding_transcript (Parent) intron:Coding_transcript (Parent,cds)
- Retired genes: a CDS feature is included. The CDS features consist of multiple parts and are unified by a common ID atribute.
CDS:history (ID)
- Non-coding genes: ncRNA and exons are available.
ncRNA:ncRNA (ID) exon:ncRNA (Parent)
- Alignment features: These features consist of multiple parts unified by a common ID attribute.
nucleotide_match:BLAT_BAC_END (ID,Target) nucleotide_match:BLAT_EST_BEST (ID,Target) nucleotide_match:BLAT_EST_OTHER (ID,Target) nucleotide_match:BLAT_NEMATODE (ID,Target) nucleotide_match:BLAT_OST_BEST (ID,Target) nucleotide_match:BLAT_OST_OTHER (ID,Target) nucleotide_match:BLAT_WASHU (ID,Target) nucleotide_match:BLAT_briggsae_est (ID,Target) nucleotide_match:BLAT_elegans_est (ID,Target) nucleotide_match:BLAT_elegans_mrna (ID,Target) nucleotide_match:BLAT_elegans_ost (ID,Target) nucleotide_match:BLAT_mRNA_BEST (ID,Target) nucleotide_match:BLAT_mRNA_OTHER (ID,Target) nucleotide_match:waba_coding (ID,Target) nucleotide_match:waba_strong (ID,Target) nucleotide_match:waba_weak (ID,Target) nucleotide_match:wublastx (ID,Target)
- Other: The remaining features are listed below.
RFLP_fragment:predicted (methods,num_reads,polymorphism) SNP:Allele (variation) chromosome:Reference (ID,Name) region:Genomic_canonical (Name,sequence) region:contig (Name,sequence)
CHANGES
WS176 - initial GFF3 and start documentation