U.S. flag

An official website of the United States government

NCBI Chaetura pelagica Annotation Release 100

The RefSeq genome records for Chaetura pelagica 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 Chaetura pelagica Annotation Release 100

Annotation release ID: 100
Date of Entrez queries for transcripts and proteins: Oct 29 2014
Date of submission of annotation to the public databases: Oct 31 2014
Software version: 6.1

Assemblies

The following assemblies were included in this annotation run:
Assembly nameAssembly accessionSubmitterAssembly dateReference/AlternateAssembly content
ChaPel_1.0GCF_000747805.1BGI09-04-2014Referenceunplaced scaffolds

Gene and feature statistics

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

Feature counts

FeatureChaPel_1.0
Genes and pseudogenes help14,275
  protein-coding14,123
  non-coding67
  pseudogenes85
  genes with variants1,082
mRNAs15,942
  fully-supported8,820
  with > 5% ab initio help3,266
  partial1,412
  with filled gap(s) help0
  known RefSeq (NM_) help0
  model RefSeq (XM_)15,942
Other RNAs help167
  fully-supported33
  with > 5% ab initio help0
  partial0
  with filled gap(s) help0
  known RefSeq (NR_) help0
  model RefSeq (XR_) help33
CDSs15,954
  fully-supported8,820
  with > 5% ab initio help3,621
  partial1,416
  with major correction(s) help966
  known RefSeq (NP_) help0
  model RefSeq (XP_) help15,942

Detailed reports

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
ChaPel_1.0GCF_000747805.17.01%19.20%

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 short reads and reported in the Short read transcript alignments section.

Transcript alignments

Short read transcript alignments

No short read transcripts were used in this annotation

Protein alignments

References