Evidence map›Paper›PMID 37249392›Full record

ArticleThe Journal of heredity2023

Chromosome-length genome assembly and karyotype of the endangered black-footed ferret (Mustela nigripes).

Sergei Kliver, Marlys L Houck, Polina L Perelman, Azamat Totikov, Andrey Tomarovsky, Olga Dudchenko, Arina D Omer, Zane Colaric, David Weisz, Erez Lieberman Aiden and 11 more

Abstract read
In one paragraph

Article in The Journal of heredity, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
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

21 authors.

Sergei KliverCenter for Evolutionary Hologenomics, The Globe Institute, The University of Copenhagen, Copenhagen, Denmark.ORCID 0000-0002-2965-3617
Marlys L HouckBeckman Center for Conservation Research, San Diego Zoo Wildlife Alliance, Escondido, CA, United States.ORCID 0000-0002-3879-9511
Polina L PerelmanDepartment of the Diversity and Evolution of Genomes, Institute of Molecular and Cellular Biology SB RAS, Novosibirsk, Russia.
Azamat TotikovDepartment of the Diversity and Evolution of Genomes, Institute of Molecular and Cellular Biology SB RAS, Novosibirsk, Russia.ORCID 0000-0003-1236-631X
Andrey TomarovskyDepartment of the Diversity and Evolution of Genomes, Institute of Molecular and Cellular Biology SB RAS, Novosibirsk, Russia.ORCID 0000-0002-6414-704X
Olga DudchenkoThe Center for Genome Architecture, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, United States.ORCID 0000-0001-9163-9544
Arina D OmerThe Center for Genome Architecture, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, United States.ORCID 0000-0003-1336-2505
Zane ColaricThe Center for Genome Architecture, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, United States.ORCID 0000-0002-6275-9616
David WeiszThe Center for Genome Architecture, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, United States.
Erez Lieberman AidenThe Center for Genome Architecture, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, United States.ORCID 0000-0003-0634-6486
Saki ChanDepartment of Research and Development, Bionano Genomics, San Diego, CA, United States.ORCID 0000-0002-2772-8208
Alex HastieDepartment of Research and Development, Bionano Genomics, San Diego, CA, United States.
Aleksey KomissarovApplied Genomics Laboratory, SCAMT Institute, ITMO University, Saint Petersburg, Russia.
Oliver A RyderBeckman Center for Conservation Research, San Diego Zoo Wildlife Alliance, Escondido, CA, United States.ORCID 0000-0003-2427-763X
Alexander GraphodatskyDepartment of the Diversity and Evolution of Genomes, Institute of Molecular and Cellular Biology SB RAS, Novosibirsk, Russia.ORCID 0000-0002-8282-1085
Warren E JohnsonCenter for Species Survival, Smithsonian's National Zoo and Conservation Biology Institute, Front Royal, VA, United States.ORCID 0000-0002-5954-186X
Jesús E MaldonadoCenter for Conservation Genomics, Smithsonian's National Zoo and Conservation Biology Institute, Washington, DC, United States.ORCID 0000-0002-4282-1072
Budhan S PukazhenthiCenter for Species Survival, Smithsonian's National Zoo and Conservation Biology Institute, Front Royal, VA, United States.ORCID 0000-0003-4657-2023
Paul E MarinariCenter for Species Survival, Smithsonian's National Zoo and Conservation Biology Institute, Front Royal, VA, United States.
David E WildtCenter for Species Survival, Smithsonian's National Zoo and Conservation Biology Institute, Front Royal, VA, United States.
Klaus-Peter KoepfliCenter for Species Survival, Smithsonian's National Zoo and Conservation Biology Institute, Front Royal, VA, United States.ORCID 0000-0001-7281-0676

Funding

Center for Genome ImagingRM1HG011016 · NHGRI · HARVARD MEDICAL SCHOOL · PI WU, CHAO-TING · 2021 to 2025
$12.2M
GENOME WIDE MAPPING OF LOOPS USING IN SITU HI-CUM1HG009375 · NHGRI · BAYLOR COLLEGE OF MEDICINE · PI LIEBERMAN-AIDEN, EREZ · 2017 to 2021
$4.7M
NHGRI NIH HHS RM1 HG011016NHGRI NIH HHS UM1 HG009375
6 · The paper itself

Abstract

The black-footed ferret (Mustela nigripes) narrowly avoided extinction to become an oft-cited example of the benefits of intensive management, research, and collaboration to save a species through ex situ conservation breeding and reintroduction into its former range. However, the species remains at risk due to possible inbreeding, disease susceptibility, and multiple fertility challenges. Here, we report the de novo genome assembly of a male black-footed ferret generated through a combination of linked-read sequencing, optical mapping, and Hi-C proximity ligation. In addition, we report the karyotype for this species, which was used to anchor and assign chromosome numbers to the chromosome-length scaffolds. The draft assembly was ~2.5 Gb in length, with 95.6% of it anchored to 19 chromosome-length scaffolds, corresponding to the 2n = 38 chromosomes revealed by the karyotype. The assembly has contig and scaffold N50 values of 148.8 kbp and 145.4 Mbp, respectively, and is up to 96% complete based on BUSCO analyses. Annotation of the assembly, including evidence from RNA-seq data, identified 21,406 protein-coding genes and a repeat content of 37.35%. Phylogenomic analyses indicated that the black-footed ferret diverged from the European polecat/domestic ferret lineage 1.6 million yr ago. This assembly will enable research on the conservation genomics of black-footed ferrets and thereby aid in the further restoration of this endangered species.

Indexed as

Endangered SpeciesFerretsAnimalsFertilityKaryotypeKaryotypingMaleannotationblack-footed ferretconservationgenome assemblykaryotypeMustela nigripes

Identifiers

PMID37249392
PMCPMC10848218

What OpenQuestion holds

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Registered trials

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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.