Evidence map›Paper›PMID 37104600›Full record

ArticleScience (New York, N.Y.)2023

Integrating gene annotation with orthology inference at scale.

Bogdan M Kirilenko, Chetan Munegowda, Ekaterina Osipova, David Jebb, Virag Sharma, Moritz Blumer, Ariadna E Morales, Alexis-Walid Ahmed, Dimitrios-Georgios Kontopoulos, Leon Hilgers and 4 more

Open access · greenAbstract read
In one paragraph

Article in Science (New York, N.Y.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 153 papers.

0numbers the graph read from it
0cells of the map it votes in
153citing papers in PubMed
28.6field-weighted citation impact, top 1% of its field
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

153 citing papers in PubMed, 186 citations in OpenAlex.

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93 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 3 institutions in 3 countries.

Bogdan M KirilenkoMax Planck Institute of Molecular Cell Biology and Genetics, 01307 Dresden, Germany.ORCID 0000-0002-9394-4275
Chetan MunegowdaMax Planck Institute of Molecular Cell Biology and Genetics, 01307 Dresden, Germany.ORCID 0000-0002-3790-2185
Ekaterina OsipovaMax Planck Institute of Molecular Cell Biology and Genetics, 01307 Dresden, Germany.ORCID 0000-0002-6769-7223
David JebbMax Planck Institute of Molecular Cell Biology and Genetics, 01307 Dresden, Germany.
Virag SharmaMax Planck Institute of Molecular Cell Biology and Genetics, 01307 Dresden, Germany.ORCID 0000-0003-4086-4105
Moritz BlumerMax Planck Institute of Molecular Cell Biology and Genetics, 01307 Dresden, Germany.ORCID 0000-0002-5775-1767
Ariadna E MoralesLOEWE Centre for Translational Biodiversity Genomics, 60325 Frankfurt, Germany.ORCID 0000-0002-0637-7349
Alexis-Walid AhmedLOEWE Centre for Translational Biodiversity Genomics, 60325 Frankfurt, Germany.
Dimitrios-Georgios KontopoulosLOEWE Centre for Translational Biodiversity Genomics, 60325 Frankfurt, Germany.ORCID 0000-0002-5082-1929
Leon HilgersLOEWE Centre for Translational Biodiversity Genomics, 60325 Frankfurt, Germany.ORCID 0000-0002-3539-2513
Kerstin Lindblad-TohScience for Life Laboratory, Department of Medical Biochemistry and Microbiology, Uppsala University, 751 32 Uppsala, Sweden.ORCID 0000-0001-8338-0253
Elinor K KarlssonBroad Institute of MIT and Harvard, Cambridge, MA 02139, USA.ORCID 0000-0002-4343-3776
Zoonomia Consortium‡
Michael HillerMax Planck Institute of Molecular Cell Biology and Genetics, 01307 Dresden, Germany.ORCID 0000-0003-3024-1449
Goethe University Frankfurt · DEBroad Institute · USMax Planck Institute for the Physics of Complex Systems · DE

Funding

GENCODE: comprehensive reference genome annotation for human and mouseU24HG007234 · NHGRI · EUROPEAN MOLECULAR BIOLOGY LABORATORY · PI Fergal James Martin · 2021 to 2026
$16.1M
The 200 mammals project: sequencing genomes by a novel cost-effective method, yielding a high resolution annotation of the human genome.R01HG008742 · NHGRI · BROAD INSTITUTE, INC. · PI BIRREN, BRUCE W., KARLSSON, ELINOR · 2016 to 2020
$2.8M
Enabling Comparative PangenomicsR01HG010485 · NHGRI · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI HAUSSLER, DAVID H, MARTIN, FERGAL JAMES · 2020 to 2023
$2.6M
NHGRI NIH HHS R01 HG008742NHGRI NIH HHS R01 HG010485NHGRI NIH HHS U24 HG007234
6 · The paper itself

Abstract

Annotating coding genes and inferring orthologs are two classical challenges in genomics and evolutionary biology that have traditionally been approached separately, limiting scalability. We present TOGA (Tool to infer Orthologs from Genome Alignments), a method that integrates structural gene annotation and orthology inference. TOGA implements a different paradigm to infer orthologous loci, improves ortholog detection and annotation of conserved genes compared with state-of-the-art methods, and handles even highly fragmented assemblies. TOGA scales to hundreds of genomes, which we demonstrate by applying it to 488 placental mammal and 501 bird assemblies, creating the largest comparative gene resources so far. Additionally, TOGA detects gene losses, enables selection screens, and automatically provides a superior measure of mammalian genome quality. TOGA is a powerful and scalable method to annotate and compare genes in the genomic era.

Indexed as

EutheriaGenomicsMolecular Sequence AnnotationAnimalsBirdsFemaleGenomeMice

Identifiers

PMID37104600
PMCPMC10193443
OpenAlexW4367173676

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.