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NCBI Nipponia nippon Annotation Release 100

The RefSeq genome records for Nipponia nippon 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 Nipponia nippon Annotation Release 100

Annotation release ID: 100
Date of Entrez queries for transcripts and proteins: Oct 3 2014
Date of submission of annotation to the public databases: Oct 7 2014
Software version: 6.1

Assemblies

The following assemblies were included in this annotation run:
Assembly nameAssembly accessionSubmitterAssembly dateReference/AlternateAssembly content
ASM70822v1GCF_000708225.1College of Medicine and Forensics, Xi'an Jiaotong University06-16-2014Reference1 assembled chromosomes; unplaced scaffolds

Gene and feature statistics

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

Feature counts

FeatureASM70822v1
Genes and pseudogenes help15,241
  protein-coding15,032
  non-coding83
  pseudogenes126
  genes with variants1,287
mRNAs17,076
  fully-supported10,196
  with > 5% ab initio help3,714
  partial1,128
  with filled gap(s) help0
  known RefSeq (NM_) help0
  model RefSeq (XM_)17,076
Other RNAs help240
  fully-supported51
  with > 5% ab initio help0
  partial0
  with filled gap(s) help0
  known RefSeq (NR_) help0
  model RefSeq (XR_) help52
CDSs17,090
  fully-supported10,196
  with > 5% ab initio help4,114
  partial1,134
  with major correction(s) help1,166
  known RefSeq (NP_) help0
  model RefSeq (XP_) help17,076

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
ASM70822v1GCF_000708225.14.41%18.22%

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