Evidence map›Paper›PMID 31915011›Full record

ArticleBMC biology2020

Long live the king: chromosome-level assembly of the lion (Panthera leo) using linked-read, Hi-C, and long-read data.

Ellie E Armstrong, Ryan W Taylor, Danny E Miller, Christopher B Kaelin, Gregory S Barsh, Elizabeth A Hadly, Dmitri Petrov

Open access · goldAbstract read
In one paragraph

Article in BMC biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

27 citing papers in PubMed, 66 citations in OpenAlex.

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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

7 authors at 4 institutions in 1 country.

Ellie E ArmstrongDepartment of Biology, Stanford University, Stanford, CA, USA. elliea@stanford.edu.ORCID 0000-0001-7107-6318
Ryan W TaylorDepartment of Biology, Stanford University, Stanford, CA, USA.
Danny E MillerDepartment of Pediatrics, Seattle Children's Hospital and The University of Washington, Seattle, WA, USA.
Christopher B KaelinHudsonAlpha Institute for Biotechnology, Huntsville, AL, USA.
Gregory S BarshHudsonAlpha Institute for Biotechnology, Huntsville, AL, USA.
Elizabeth A HadlyDepartment of Biology, Stanford University, Stanford, CA, USA.
Dmitri PetrovDepartment of Biology, Stanford University, Stanford, CA, USA.
Stanford University · USHudsonAlpha Institute for Biotechnology · USSeattle Children's Hospital · USUniversity of California, Davis · US

Funding

Genomics of rapid adaptation in the lab and in the wildR35GM118165 · NIGMS · STANFORD UNIVERSITY · PI Dmitri Petrov · 2016 to 2026
$8.3M
Melanocortin signaling: genetic insight from X-linked color mutations in non-model organismsR01AR067925 · NIAMS · HUDSON-ALPHA INSTITUTE FOR BIOTECHNOLOGY · PI BARSH, GREGORY STEFAN · 2015 to 2019
$1.6M
NIAMS NIH HHS R01 AR067925NIGMS NIH HHS R35 GM118165
6 · The paper itself

Abstract

backgroundThe lion (Panthera leo) is one of the most popular and iconic feline species on the planet, yet in spite of its popularity, the last century has seen massive declines for lion populations worldwide. Genomic resources for endangered species represent an important way forward for the field of conservation, enabling high-resolution studies of demography, disease, and population dynamics. Here, we present a chromosome-level assembly from a captive African lion from the Exotic Feline Rescue Center (Center Point, IN) as a resource for current and subsequent genetic work of the sole social species of the Panthera clade.

resultsOur assembly is composed of 10x Genomics Chromium data, Dovetail Hi-C, and Oxford Nanopore long-read data. Synteny is highly conserved between the lion, other Panthera genomes, and the domestic cat. We find variability in the length of runs of homozygosity across lion genomes, indicating contrasting histories of recent and possibly intense inbreeding and bottleneck events. Demographic analyses reveal similar ancient histories across all individuals during the Pleistocene except the Asiatic lion, which shows a more rapid decline in population size. We show a substantial influence on the reference genome choice in the inference of demographic history and heterozygosity.

conclusionsWe demonstrate that the choice of reference genome is important when comparing heterozygosity estimates across species and those inferred from different references should not be compared to each other. In addition, estimates of heterozygosity or the amount or length of runs of homozygosity should not be taken as reflective of a species, as these can differ substantially among individuals. This high-quality genome will greatly aid in the continuing research and conservation efforts for the lion, which is rapidly moving towards becoming a species in danger of extinction.

Indexed as

GenomeAnimalsFemaleLionsSynteny10x Genomics ChromiumAfrican lionConservation genomicsDovetail Hi-CGenome assemblyOxford NanoporePanthera leoReference bias

Identifiers

PMID31915011
PMCPMC6950864
OpenAlexW3000431709

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.