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NCBI Aotus nancymaae Annotation Release GCF_030222135.1-RS_2024_04

The genome sequence records for Aotus nancymaae RefSeq assembly GCF_030222135.1 (86718_ANA_hifiasm-v0.15.2.pri) 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_030222135.1-RS_2024_04".

Date of Entrez queries for transcripts and proteins: Apr 7 2024
Date of submission of annotation to the public databases: Apr 10 2024
Software version: 10.2

Assemblies

The following assemblies were included in this annotation run:
Assembly nameAssembly accessionSubmitterAssembly dateReference/AlternateAssembly content
86718_ANA_hifiasm-v0.15.2.priGCF_030222135.1University of Washington06-07-2023Reference1 assembled chromosomes; unplaced scaffolds

Gene and feature statistics

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

Feature counts

Feature86718_ANA_hifiasm-v0.15.2.pri
Genes and pseudogenes help37,568
  protein-coding21,779
  non-coding8,248
  Transcribed pseudogenes18
  Non-transcribed pseudogenes7,431
  genes with variants11,558
  Immunoglobulin/T-cell receptor gene segments45
  other47
mRNAs56,480
  fully-supported54,991
  with > 5% ab initio help766
  partial91
  with filled gap(s) help0
  known RefSeq (NM_) help18
  model RefSeq (XM_)56,462
non-coding RNAs help12,075
  fully-supported7,448
  with > 5% ab initio help0
  partial1
  with filled gap(s) help0
  known RefSeq (NR_) help0
  model RefSeq (XR_) help11,619
pseudo transcripts help18
  fully-supported14
  with > 5% ab initio help0
  partial0
  with filled gap(s) help0
  known RefSeq (NR_) help0
  model RefSeq (XR_) help18
CDSs56,538
  fully-supported54,991
  with > 5% ab initio help885
  partial91
  with major correction(s) help1,194
  known RefSeq (NP_) help18
  model RefSeq (XP_) help56,475

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 primates_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 21766 coding genes, 21443 genes had a protein with an alignment covering 50% or more of the query and 19251 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
86718_ANA_hifiasm-v0.15.2.priGCF_030222135.143.67%

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:

Assembly-assembly alignments of current to previous assembly

When the assembly changes between two rounds of annotation, genes in the current and the previous annotation are mapped to each other using the genomic alignments of the current assembly to the previous assembly so that gene identifiers can be preserved. The success of the remapping depends largely on how well the two assembly versions align to each other.

Below are the percent coverage of one assembly by the other and the average percent identity of the alignments. The 'First pass' alignments are reciprocal best hits, while the 'Total' alignments also include 'Second pass' or non-reciprocal best alignments.

First PassTotal
86718_ANA_hifiasm-v0.15.2.pri (Current) Coverage: 82.38%86718_ANA_hifiasm-v0.15.2.pri (Current) Coverage: 83.65%
Anan_2.0 (Previous) Coverage: 94.00%Anan_2.0 (Previous) Coverage: 97.72%
Percent Identity: 93.30%Percent Identity: 93.47%

Comparison of the current and previous annotations

The annotations produced for this release were compared to the annotations in the previous release for each assembly annotated in both releases. Scores for current and previous gene and transcript features were calculated based on overlap in exon sequence and matches in exon boundaries. Pairs of current and previous features were categorized based on these scores, whether they are reciprocal best matches, and changes in attributes (gene biotype, completeness, etc.). If the assembly was updated between the two releases, alignments between the current and the previous assembly were used to match the current and previous gene and transcript features in mapped regions.

The table below summarizes the changes in the gene set for each assembly as a percent of the number of genes in the current annotation release, and provides a link to the details of the comparison in tabular format.

86718_ANA_hifiasm-v0.15.2.pri (Current) to Anan_2.0 (Previous)
Identical help7%
Minor changes help46%
Major changes help18%
New help27%
Deprecated help11%
Other help1%
Download the reporttabular

References