Evidence map›Paper›PMID 27882922›Full record

ArticleNature communications2016

An ethnically relevant consensus Korean reference genome is a step towards personal reference genomes.

Yun Sung Cho, Hyunho Kim, Hak-Min Kim, Sungwoong Jho, JeHoon Jun, Yong Joo Lee, Kyun Shik Chae, Chang Geun Kim, Sangsoo Kim, Anders Eriksson and 7 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Nature communications, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
4.4field-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

45 citing papers in PubMed, 85 citations in OpenAlex.

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  20. LazyB: fast and cheap genome assembly.Algorithms for molecular biology : AMB · 2021
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 8 institutions in 4 countries.

Yun Sung ChoThe Genomics Institute (TGI), Ulsan National Institute of Science and Technology (UNIST), Ulsan 44919, Korea.
Hyunho KimGeromics Inc., Ulsan National Institute of Science and Technology (UNIST), Ulsan 44919, Korea.
Hak-Min KimThe Genomics Institute (TGI), Ulsan National Institute of Science and Technology (UNIST), Ulsan 44919, Korea.
Sungwoong JhoPersonal Genomics Institute, Genome Research Foundation, Cheongju 28160, Korea.
JeHoon JunPersonal Genomics Institute, Genome Research Foundation, Cheongju 28160, Korea.
Yong Joo LeeGeromics Inc., Ulsan National Institute of Science and Technology (UNIST), Ulsan 44919, Korea.
Kyun Shik ChaeNational Standard Reference Center, Korea Research Institute of Standards and Science, Daejeon 34113, Korea.
Chang Geun KimNational Standard Reference Center, Korea Research Institute of Standards and Science, Daejeon 34113, Korea.
Sangsoo KimSchool of Systems Biomedical Science, Soongsil University, Seoul 06978, Korea.
Anders ErikssonDepartment of Zoology, University of Cambridge, Downing Street, Cambridge CB2 3EJ, UK.ORCID 0000-0003-3436-3726
Jeremy S EdwardsChemistry and Chemical Biology, UNM Comprehensive Cancer Center, University of New Mexico, Albuquerque, New Mexico 87131, USA.
Semin LeeThe Genomics Institute (TGI), Ulsan National Institute of Science and Technology (UNIST), Ulsan 44919, Korea.
Byung Chul KimThe Genomics Institute (TGI), Ulsan National Institute of Science and Technology (UNIST), Ulsan 44919, Korea.
Andrea ManicaDepartment of Zoology, University of Cambridge, Downing Street, Cambridge CB2 3EJ, UK.ORCID 0000-0003-1895-450X
Tae-Kwang OhInfection and Immunity Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon 34141, Korea.
George M ChurchDepartment of Genetics, New Research Building (NRB), Harvard Medical School, 77 Avenue Louis Pasteur, Room 238, Boston, Massachusetts 02115, USA.
Jong BhakThe Genomics Institute (TGI), Ulsan National Institute of Science and Technology (UNIST), Ulsan 44919, Korea.
Ulsan National Institute of Science and Technology · KRGenome Research Foundation · KRKorea Research Institute of Standards and Science · KRUniversity of Cambridge · GBHarvard University · USKorea Research Institute of Bioscience and Biotechnology · KRSoongsil University · KRUniversity of New Mexico · US

Funding

Haplotype Resolved Sequencing TechnologyR01HG006876 · NHGRI · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI EDWARDS, JEREMY S · 2013 to 2015
$1.3M
NHGRI NIH HHS R01 HG006876
6 · The paper itself

Abstract

Human genomes are routinely compared against a universal reference. However, this strategy could miss population-specific and personal genomic variations, which may be detected more efficiently using an ethnically relevant or personal reference. Here we report a hybrid assembly of a Korean reference genome (KOREF) for constructing personal and ethnic references by combining sequencing and mapping methods. We also build its consensus variome reference, providing information on millions of variants from 40 additional ethnically homogeneous genomes from the Korean Personal Genome Project. We find that the ethnically relevant consensus reference can be beneficial for efficient variant detection. Systematic comparison of human assemblies shows the importance of assembly quality, suggesting the necessity of new technologies to comprehensively map ethnic and personal genomic structure variations. In the era of large-scale population genome projects, the leveraging of ethnicity-specific genome assemblies as well as the human reference genome will accelerate mapping all human genome diversity.

Indexed as

Asian PeopleChromosome MappingConsensusGenome, HumanHigh-Throughput Nucleotide SequencingHumansRepublic of KoreaSequence Analysis, DNA

Identifiers

PMID27882922
PMCPMC5123046
OpenAlexW2552622726

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.