NCBI Humulus lupulus Annotation Release GCF_963169125.1-RS_2024_01

The genome sequence records for Humulus lupulus RefSeq assembly GCF_963169125.1 (drHumLupu1.1) were annotated by the NCBI Eukaryotic Genome Annotation Pipeline, an automated pipeline that annotates genes, transcripts and proteins on draft and finished genome assemblies.

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_963169125.1-RS_2024_01".

Date of Entrez queries for transcripts and proteins: Jan 4 2024
Date of submission of annotation to the public databases: Jan 9 2024
Software version: 10.2

Assemblies

The following assemblies were included in this annotation run:
Assembly nameAssembly accessionSubmitterAssembly dateReference/AlternateAssembly content
drHumLupu1.1GCF_963169125.1WELLCOME SANGER INSTITUTE08-19-2023Reference10 assembled chromosomes; unplaced scaffolds

Gene and feature statistics

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

Feature counts

FeaturedrHumLupu1.1
Genes and pseudogenes help57,465
  protein-coding35,582
  non-coding19,381
  Transcribed pseudogenes7
  Non-transcribed pseudogenes2,495
  genes with variants7,832
  Immunoglobulin/T-cell receptor gene segments0
  other0
mRNAs47,669
  fully-supported34,903
  with > 5% ab initio help11,664
  partial224
  with filled gap(s) help22
  known RefSeq (NM_) help0
  model RefSeq (XM_)47,669
non-coding RNAs help25,462
  fully-supported12,235
  with > 5% ab initio help0
  partial7
  with filled gap(s) help0
  known RefSeq (NR_) help0
  model RefSeq (XR_) help24,937
pseudo transcripts help7
  fully-supported6
  with > 5% ab initio help0
  partial0
  with filled gap(s) help0
  known RefSeq (NR_) help0
  model RefSeq (XR_) help7
CDSs47,669
  fully-supported34,903
  with > 5% ab initio help11,848
  partial219
  with major correction(s) help67
  known RefSeq (NP_) help0
  model RefSeq (XP_) help47,669

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 eudicots_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 Arabidopsis thaliana known RefSeq proteins, using the annotated proteins as the query and the high-quality proteins as the target. Out of 35582 coding genes, 27370 genes had a protein with an alignment covering 50% or more of the query and 10669 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: Arabidopsis thaliana known RefSeq 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
drHumLupu1.1GCF_963169125.160.68%

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)

SRA Long Read Alignment Statistics

The alignments of the following long RNA-Seq reads (PacBio, Oxford Nanopore, 454, or other long-read sequencing technologies) from the Sequence Read Archive with minimap2 were used for gene prediction:

Protein alignments

The alignments of the following proteins with ProSplign were used for gene prediction:

References