Evidence map›Paper›PMID 29145861›Full record

ArticleBMC biology2017

Hybrid de novo genome assembly and centromere characterization of the gray mouse lemur (Microcebus murinus).

Peter A Larsen, R Alan Harris, Yue Liu, Shwetha C Murali, C Ryan Campbell, Adam D Brown, Beth A Sullivan, Jennifer Shelton, Susan J Brown, Muthuswamy Raveendran and 10 more

Open access · goldAbstract read
In one paragraph

Article in BMC biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
3.9field-weighted citation impact, top 5% 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

38 citing papers in PubMed, 78 citations in OpenAlex.

  1. Rapid centromere turnover and the adaptive radiation of lemurs.bioRxiv : the preprint server for biology · 2026
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  9. Ecology and evolution · 2025
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  11. eLemur: A cellular-resolution 3D atlas of the mouse lemur brain.Proceedings of the National Academy of Sciences of the United States of America · 2024
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  16. CebidaeLife (Basel, Switzerland) · 2022
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  17. Functional genomics analysis reveals the evolutionary adaptation and demographic history of pygmy lorises.Proceedings of the National Academy of Sciences of the United States of America · 2022
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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

20 authors at 4 institutions in 2 countries.

Peter A LarsenDepartment of Biology, Duke University, Durham, NC, 27708, USA. peter.larsen@duke.edu.ORCID http://orcid.org/0000-0002-3634-3625
R Alan HarrisHuman Genome Sequencing Center, Baylor College of Medicine, Houston, TX, 77030, USA.
Yue LiuHuman Genome Sequencing Center, Baylor College of Medicine, Houston, TX, 77030, USA.
Shwetha C MuraliHuman Genome Sequencing Center, Baylor College of Medicine, Houston, TX, 77030, USA.
C Ryan CampbellDepartment of Biology, Duke University, Durham, NC, 27708, USA.
Adam D BrownDepartment of Pharmacology and Cancer Biology, Duke University, Durham, NC, 27710, USA.
Beth A SullivanDepartment of Molecular Genetics and Microbiology, Duke University, Durham, NC, 27710, USA.
Jennifer SheltonKansas State University Bioinformatics Center, Division of Biology, Kansas State University, Manhattan, KS, 66506, USA.
Susan J BrownKansas State University Bioinformatics Center, Division of Biology, Kansas State University, Manhattan, KS, 66506, USA.
Muthuswamy RaveendranHuman Genome Sequencing Center, Baylor College of Medicine, Houston, TX, 77030, USA.
Olga DudchenkoDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.
Ido MacholDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.
Neva C DurandDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.
Muhammad S ShamimDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.
Erez Lieberman AidenDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, 77030, USA.
Donna M MuznyHuman Genome Sequencing Center, Baylor College of Medicine, Houston, TX, 77030, USA.
Richard A GibbsHuman Genome Sequencing Center, Baylor College of Medicine, Houston, TX, 77030, USA.
Anne D YoderDepartment of Biology, Duke University, Durham, NC, 27708, USA.
Jeffrey RogersHuman Genome Sequencing Center, Baylor College of Medicine, Houston, TX, 77030, USA.
Kim C WorleyHuman Genome Sequencing Center, Baylor College of Medicine, Houston, TX, 77030, USA.
Baylor College of Medicine · USDuke University · USKansas State University · USBristol-Myers Squibb (Germany) · DE

Funding

The Human Genome Sequencing CenterU54HG003273 · NHGRI · BAYLOR COLLEGE OF MEDICINE · PI GIBBS, RICHARD A · 2004 to 2015
$341.3M
Mentoring CoreP20GM103418 · NIGMS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI SUSAN J. BROWN · 2012 to 2026
$63.0M
Genomic Analysis of Centromere Assembly and FunctionR01GM124041 · NIGMS · DUKE UNIVERSITY · PI SULLIVAN, BETH A · 2017 to 2025
$2.8M
Data commons for 'omic, microscopy and analysis core facilitiesS10OD018164 · OD · DUKE UNIVERSITY · PI WRAY, GREGORY A. · 2014 to 2014
$598k
NHGRI NIH HHS U54 HG003273NIGMS NIH HHS P20 GM103418NIGMS NIH HHS R01 GM124041NIH HHS S10 OD018164
6 · The paper itself

Abstract

backgroundThe de novo assembly of repeat-rich mammalian genomes using only high-throughput short read sequencing data typically results in highly fragmented genome assemblies that limit downstream applications. Here, we present an iterative approach to hybrid de novo genome assembly that incorporates datasets stemming from multiple genomic technologies and methods. We used this approach to improve the gray mouse lemur (Microcebus murinus) genome from early draft status to a near chromosome-scale assembly.

methodsWe used a combination of advanced genomic technologies to iteratively resolve conflicts and super-scaffold the M. murinus genome.

resultsWe improved the M. murinus genome assembly to a scaffold N50 of 93.32 Mb. Whole genome alignments between our primary super-scaffolds and 23 human chromosomes revealed patterns that are congruent with historical comparative cytogenetic data, thus demonstrating the accuracy of our de novo scaffolding approach and allowing assignment of scaffolds to M. murinus chromosomes. Moreover, we utilized our independent datasets to discover and characterize sequences associated with centromeres across the mouse lemur genome. Quality assessment of the final assembly found 96% of mouse lemur canonical transcripts nearly complete, comparable to other published high-quality reference genome assemblies.

conclusionsWe describe a new assembly of the gray mouse lemur (Microcebus murinus) genome with chromosome-scale scaffolds produced using a hybrid bioinformatic and sequencing approach. The approach is cost effective and produces superior results based on metrics of contiguity and completeness. Our results show that emerging genomic technologies can be used in combination to characterize centromeres of non-model species and to produce accurate de novo chromosome-scale genome assemblies of complex mammalian genomes.

Indexed as

GenomeAnimalsCentromereCheirogaleidaeComputational BiologyFemaleHigh-Throughput Nucleotide SequencingSequence Analysis, DNACentromeresde novo assemblyHi-COptical mapsPhysical mapsStrepsirrhine primateSuper-scaffolding

Identifiers

PMID29145861
PMCPMC5689209
OpenAlexW2770815541

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.