ArticleF1000Research2022
Manual annotation of
Article in F1000Research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 82 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
82 citing papers in PubMed, 23 citations in OpenAlex.
- Gene model for the ortholog ofbioRxiv : the preprint server for biology · 2026Article
- Gene model for the ortholog ofbioRxiv : the preprint server for biology · 2026Article
- Gene model for the ortholog ofbioRxiv : the preprint server for biology · 2026Article
- Gene model for the ortholog ofbioRxiv : the preprint server for biology · 2026Article
- Gene model for the ortholog ofbioRxiv : the preprint server for biology · 2026Article
- Gene model for the ortholog ofbioRxiv : the preprint server for biology · 2026Article
- Gene model for the ortholog ofbioRxiv : the preprint server for biology · 2026Article
- Gene model for the ortholog ofbioRxiv : the preprint server for biology · 2026Article
- Gene model for the ortholog ofbioRxiv : the preprint server for biology · 2026Article
- Gene model for the ortholog ofbioRxiv : the preprint server for biology · 2026Article
- Gene model for the ortholog ofmicroPublication biology · 2026Article
- Gene model for the ortholog ofmicroPublication biology · 2026Article
- Gene model for the ortholog ofmicroPublication biology · 2026Article
- Gene Model for the ortholog ofmicroPublication biology · 2026Article
- Gene model for the ortholog ofmicroPublication biology · 2026Article
- Gene model for the ortholog ofmicroPublication biology · 2026Article
- Gene model for the ortholog ofmicroPublication biology · 2026Article
- Gene model for the ortholog ofmicroPublication biology · 2026Article
- Gene model for the ortholog ofmicroPublication biology · 2026Article
- Gene model for the ortholog ofmicroPublication biology · 2026Article
22 more citing papers are in PubMed but not listed here.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors at 2 institutions in 1 country.
Funding
Abstract
Annotating the genomes of multiple species allows us to analyze the evolution of their genes. While many eukaryotic genome assemblies already include computational gene predictions, these predictions can benefit from review and refinement through manual gene annotation. The Genomics Education Partnership (GEP; https://thegep.org/) developed a structural annotation protocol for protein-coding genes that enables undergraduate student and faculty researchers to create high-quality gene annotations that can be utilized in subsequent scientific investigations. For example, this protocol has been utilized by the GEP faculty to engage undergraduate students in the comparative annotation of genes involved in the insulin signaling pathway in 27
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.