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NCBI Morone saxatilis Annotation Release 100

The RefSeq genome records for Morone saxatilis 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 Morone saxatilis Annotation Release 100

Annotation release ID: 100
Date of Entrez queries for transcripts and proteins: Jul 22 2020
Date of submission of annotation to the public databases: Jul 27 2020
Software version: 8.5

Assemblies

The following assemblies were included in this annotation run:
Assembly nameAssembly accessionSubmitterAssembly dateReference/AlternateAssembly content
NCSU_SB_2.0GCF_004916995.1North Carolina State University04-26-2019Reference1 assembled chromosomes; unplaced scaffolds

Gene and feature statistics

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

Feature counts

FeatureNCSU_SB_2.0
Genes and pseudogenes help23,020
  protein-coding21,640
  non-coding1,100
  transcribed pseudogenes0
  non-transcribed pseudogenes274
  genes with variants4,807
  immunoglobulin/T-cell receptor gene segments6
  other0
mRNAs30,899
  fully-supported28,013
  with > 5% ab initio help1,144
  partial4,142
  with filled gap(s) help3,887
  known RefSeq (NM_) help0
  model RefSeq (XM_)30,899
non-coding RNAs help1,437
  fully-supported982
  with > 5% ab initio help0
  partial20
  with filled gap(s) help20
  known RefSeq (NR_) help0
  model RefSeq (XR_) help1,191
pseudo transcripts help0
  fully-supported0
  with > 5% ab initio help0
  partial0
  with filled gap(s) help0
  known RefSeq (NR_) help0
  model RefSeq (XR_) help0
CDSs30,918
  fully-supported28,013
  with > 5% ab initio help1,408
  partial3,543
  with major correction(s) help2,035
  known RefSeq (NP_) help0
  model RefSeq (XP_) help30,912

Detailed reports

The counts below do not include pseudogenes.

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 21627 coding genes, 20308 genes had a protein with an alignment covering 50% or more of the query and 9548 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 for each assembly. RepeatMasker results are only used for organisms for which a comprehensive repeat library is available.

For this annotation run, transcripts and proteins were aligned to the genome masked with WindowMasker only.
Assembly nameAssembly accession% Masked with RepeatMasker% Masked with WindowMasker
NCSU_SB_2.0GCF_004916995.12.57%22.03%

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, aligned to the genome by Splign or ProSplign and passed to Gnomon, NCBI's gene prediction software.

Depending on the other evidence available, long 454 reads (with average length above 250 nt) may be aligned as traditional evidence and reported in the Transcript alignments section or aligned with RNA-Seq reads and reported in the RNA-Seq alignments section.

Transcript alignments

RNA-Seq alignments

The following RNA-Seq reads from the Sequence Read Archive 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

References