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NCBI Panonychus citri Annotation Release GCF_014898815.1-RS_2023_01

The RefSeq genome records for Panonychus citri 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 "GCF_014898815.1-RS_2023_01".

Date of Entrez queries for transcripts and proteins: Jan 26 2023
Date of submission of annotation to the public databases: Jan 30 2023
Software version: 10.1

Assemblies

The following assemblies were included in this annotation run:
Assembly nameAssembly accessionSubmitterAssembly dateReference/AlternateAssembly content
ASM1489881v1GCF_014898815.1Citrus Research Institute, Southwest University/Chinese Academy of Agricultural Sciences10-20-2020Reference1 assembled chromosomes; unplaced scaffolds

Gene and feature statistics

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

Feature counts

FeatureASM1489881v1
Genes and pseudogenes help12,885
  protein-coding11,460
  non-coding1,055
  Transcribed pseudogenes1
  Non-transcribed pseudogenes369
  genes with variants2,399
  Immunoglobulin/T-cell receptor gene segments0
  other0
mRNAs14,849
  fully-supported13,777
  with > 5% ab initio help667
  partial154
  with filled gap(s) help0
  known RefSeq (NM_) help0
  model RefSeq (XM_)14,849
non-coding RNAs help2,530
  fully-supported2,340
  with > 5% ab initio help0
  partial0
  with filled gap(s) help0
  known RefSeq (NR_) help0
  model RefSeq (XR_) help2,388
pseudo transcripts help1
  fully-supported1
  with > 5% ab initio help0
  partial0
  with filled gap(s) help0
  known RefSeq (NR_) help0
  model RefSeq (XR_) help1
CDSs14,862
  fully-supported13,777
  with > 5% ab initio help718
  partial154
  with major correction(s) help1,093
  known RefSeq (NP_) help0
  model RefSeq (XP_) help14,862

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 arachnida_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 11447 coding genes, 8250 genes had a protein with an alignment covering 50% or more of the query and 1634 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
ASM1489881v1GCF_014898815.136.46%

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