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NCBI Falco peregrinus Annotation Release 102

The RefSeq genome records for Falco peregrinus 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 Falco peregrinus Annotation Release 102

Annotation release ID: 102
Date of Entrez queries for transcripts and proteins: Jan 18 2019
Date of submission of annotation to the public databases: Jan 24 2019
Software version: 8.1

Assemblies

The following assemblies were included in this annotation run:
Assembly nameAssembly accessionSubmitterAssembly dateReference/AlternateAssembly content
F_peregrinus_v1.0GCF_000337955.1BGI02-05-2013Reference1 assembled chromosomes; unplaced scaffolds

Gene and feature statistics

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

Feature counts

FeatureF_peregrinus_v1.0
Genes and pseudogenes help18,971
  protein-coding15,230
  non-coding3,632
  transcribed pseudogenes6
  non-transcribed pseudogenes91
  genes with variants6,260
  immunoglobulin/T-cell receptor gene segments12
  other0
mRNAs31,127
  fully-supported28,354
  with > 5% ab initio help855
  partial1,354
  with filled gap(s) help0
  known RefSeq (NM_) help11
  model RefSeq (XM_)31,116
non-coding RNAs help6,594
  fully-supported6,130
  with > 5% ab initio help0
  partial2
  with filled gap(s) help0
  known RefSeq (NR_) help0
  model RefSeq (XR_) help6,373
pseudo transcripts help6
  fully-supported4
  with > 5% ab initio help0
  partial0
  with filled gap(s) help0
  known RefSeq (NR_) help0
  model RefSeq (XR_) help6
CDSs31,152
  fully-supported28,354
  with > 5% ab initio help1,310
  partial1,355
  with major correction(s) help1,220
  known RefSeq (NP_) help24
  model RefSeq (XP_) help31,116

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 15217 coding genes, 14828 genes had a protein with an alignment covering 50% or more of the query and 9487 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
F_peregrinus_v1.0GCF_000337955.15.23%17.91%

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

Comparison of the current and previous annotations

The annotation produced for this release (102) was compared to the annotation in the previous release (101) 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 links to the details of the comparison in tabular format and in a Genome Workbench project.

F_peregrinus_v1.0 (Current) to F_peregrinus_v1.0 (Previous)
Identical help2%
Minor changes help58%
Major changes help18%
New help20%
Deprecated help2%
Other help2%
Download the reporttabular, Genome Workbench

References