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NCBI Bubalus carabanensis Annotation Release GCF_029407905.1-RS_2023_04

The genome sequence records for Bubalus carabanensis RefSeq assembly GCF_029407905.1 (PCC_UOA_SB_1v2) were annotated by the NCBI Eukaryotic Genome Annotation Pipeline, an automated pipeline that annotates genes, transcripts and proteins on draft and finished genome assemblies.

The annotation products are available in the sequence databases and on the FTP site.

This report provides:

For more information on the annotation process, please visit the NCBI Eukaryotic Genome Annotation Pipeline page.


Annotation Release information

This annotation should be referred to as "GCF_029407905.1-RS_2023_04".

Date of Entrez queries for transcripts and proteins: Apr 20 2023
Date of submission of annotation to the public databases: Apr 25 2023
Software version: 10.1

Assemblies

The following assemblies were included in this annotation run:
Assembly nameAssembly accessionSubmitterAssembly dateReference/AlternateAssembly content
PCC_UOA_SB_1v2GCF_029407905.1University of Adelaide03-31-2023Reference24 assembled chromosomes; unplaced scaffolds

Gene and feature statistics

Counts and length of annotated features are provided below for each assembly.

Feature counts

FeaturePCC_UOA_SB_1v2
Genes and pseudogenes help40,636
  protein-coding21,871
  non-coding13,688
  Transcribed pseudogenes0
  Non-transcribed pseudogenes4,726
  genes with variants12,446
  Immunoglobulin/T-cell receptor gene segments319
  other32
mRNAs56,815
  fully-supported54,730
  with > 5% ab initio help1,069
  partial97
  with filled gap(s) help0
  known RefSeq (NM_) help0
  model RefSeq (XM_)56,815
non-coding RNAs help22,968
  fully-supported18,618
  with > 5% ab initio help0
  partial0
  with filled gap(s) help0
  known RefSeq (NR_) help0
  model RefSeq (XR_) help20,464
pseudo transcripts help0
  fully-supported0
  with > 5% ab initio help0
  partial0
  with filled gap(s) help0
  known RefSeq (NR_) help0
  model RefSeq (XR_) help0
CDSs57,134
  fully-supported54,730
  with > 5% ab initio help1,220
  partial102
  with major correction(s) help586
  known RefSeq (NP_) help0
  model RefSeq (XP_) help56,815

Detailed reports

The counts below do not include pseudogenes.

BUSCO analysis of gene annotation

BUSCO v4.1.4 was run in "protein" mode on the annotated gene set picking one longest protein per gene, and run using the cetartiodactyla_odb10 lineage dataset. Results are reported for the gene set from the primary assembly unit, and presented in BUSCO notation.

Alignment of the annotated proteins to a set of high-quality proteins

The final set of annotated proteins was searched with BLASTP against the UniProtKB/Swiss-Prot curated proteins, using the annotated proteins as the query and the high-quality proteins as the target. Out of 21871 coding genes, 21410 genes had a protein with an alignment covering 50% or more of the query and 18182 had an alignment covering 95% or more of the query.

Definition of query and target coverage. The query coverage is the percentage of the annotated protein length that is included in the alignment. The target coverage is the percentage of the target length that is included in the alignment.

Below is a cumulative graph displaying the number of genes with alignments above a given query or target coverage threshold. For comparison, corresponding statistics for other organisms annotated by the NCBI eukaryotic annotation pipeline were added to the graph.

Query: annotated proteins
Target: UniProtKB/Swiss-Prot curated proteins

Masking of genomic sequence

Transcript and protein alignments are performed on the repeat-masked genome. Below are the percentages of genomic sequence masked by WindowMasker and RepeatMasker (if calculated), for each assembly. RepeatMasker results are only calculated for organisms with complete Dfam HMM model collections.

For this annotation run, transcripts and proteins were aligned to the genome masked with WindowMasker only.
Assembly nameAssembly accession% Masked with WindowMasker
PCC_UOA_SB_1v2GCF_029407905.144.70%

Transcript and protein alignments

The annotation pipeline relies heavily on alignments of experimental evidence for gene prediction. Below are the sets of transcripts and proteins that were retrieved from Entrez Nucleotide, Entrez Protein, and SRA, and aligned to the genome.

Transcript alignments

The alignments of the following transcripts with Splign were used for gene prediction:

RNA-Seq alignments

The alignments of the following RNA-Seq reads with STAR were also used for gene prediction:

  Hide alignments statistics, by sample (SAME, SAMN, SAMD, DRS)
  Show alignments statistics, by run (ERR, SRR, DRR)

Protein alignments

The alignments of the following proteins with ProSplign were used for gene prediction:

References