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NCBI Gopherus flavomarginatus Annotation Release 100

The RefSeq genome records for Gopherus flavomarginatus were annotated by the NCBI Eukaryotic Genome Annotation Pipeline, an automated pipeline that annotates genes, transcripts and proteins on draft and finished genome assemblies. This report presents statistics on the annotation products, the input data used in the pipeline and intermediate alignment results.

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 NCBI Gopherus flavomarginatus Annotation Release 100

Annotation release ID: 100
Date of Entrez queries for transcripts and proteins: Sep 29 2022
Date of submission of annotation to the public databases: Oct 2 2022
Software version: 10.0

Assemblies

The following assemblies were included in this annotation run:
Assembly nameAssembly accessionSubmitterAssembly dateReference/AlternateAssembly content
rGopFla2.mat.asmGCF_025201925.1Vertebrate Genomes Project09-15-2022Reference25 assembled chromosomes; unplaced scaffolds

Gene and feature statistics

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

Feature counts

FeaturerGopFla2.mat.asm
Genes and pseudogenes help29,021
  protein-coding20,882
  non-coding6,569
  Transcribed pseudogenes0
  Non-transcribed pseudogenes1,402
  genes with variants11,115
  Immunoglobulin/T-cell receptor gene segments151
  other17
mRNAs53,745
  fully-supported51,697
  with > 5% ab initio help926
  partial97
  with filled gap(s) help0
  known RefSeq (NM_) help0
  model RefSeq (XM_)53,745
non-coding RNAs help11,077
  fully-supported7,447
  with > 5% ab initio help0
  partial0
  with filled gap(s) help0
  known RefSeq (NR_) help0
  model RefSeq (XR_) help8,262
pseudo transcripts help0
  fully-supported0
  with > 5% ab initio help0
  partial0
  with filled gap(s) help0
  known RefSeq (NR_) help0
  model RefSeq (XR_) help0
CDSs53,896
  fully-supported51,697
  with > 5% ab initio help1,067
  partial101
  with major correction(s) help517
  known RefSeq (NP_) help0
  model RefSeq (XP_) help53,745

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 sauropsida_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 20882 coding genes, 19791 genes had a protein with an alignment covering 50% or more of the query and 12915 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
rGopFla2.mat.asmGCF_025201925.134.08%

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:

No transcript evidence was used in this annotation

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