Evidence map›Paper›PMID 28079141›Full record

ArticleScientific reports2017

Development of a 690 K SNP array in catfish and its application for genetic mapping and validation of the reference genome sequence.

Qifan Zeng, Qiang Fu, Yun Li, Geoff Waldbieser, Brian Bosworth, Shikai Liu, Yujia Yang, Lisui Bao, Zihao Yuan, Ning Li and 1 more

Abstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing 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

32 citing papers in PubMed.

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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

11 authors.

Qifan ZengThe Fish Molecular Genetics and Biotechnology Laboratory, School of Fisheries, Aquaculture, and Aquatic Sciences, and Program of Cell and Molecular Biosciences, Auburn University, Auburn, Alabama 36849, United States of America.
Qiang FuThe Fish Molecular Genetics and Biotechnology Laboratory, School of Fisheries, Aquaculture, and Aquatic Sciences, and Program of Cell and Molecular Biosciences, Auburn University, Auburn, Alabama 36849, United States of America.
Yun LiThe Fish Molecular Genetics and Biotechnology Laboratory, School of Fisheries, Aquaculture, and Aquatic Sciences, and Program of Cell and Molecular Biosciences, Auburn University, Auburn, Alabama 36849, United States of America.
Geoff WaldbieserUSDA-ARS Warmwater Aquaculture Research Unit, Stoneville, Mississippi 38776, United States of America.
Brian BosworthUSDA-ARS Warmwater Aquaculture Research Unit, Stoneville, Mississippi 38776, United States of America.
Shikai LiuThe Fish Molecular Genetics and Biotechnology Laboratory, School of Fisheries, Aquaculture, and Aquatic Sciences, and Program of Cell and Molecular Biosciences, Auburn University, Auburn, Alabama 36849, United States of America.
Yujia YangThe Fish Molecular Genetics and Biotechnology Laboratory, School of Fisheries, Aquaculture, and Aquatic Sciences, and Program of Cell and Molecular Biosciences, Auburn University, Auburn, Alabama 36849, United States of America.
Lisui BaoThe Fish Molecular Genetics and Biotechnology Laboratory, School of Fisheries, Aquaculture, and Aquatic Sciences, and Program of Cell and Molecular Biosciences, Auburn University, Auburn, Alabama 36849, United States of America.
Zihao YuanThe Fish Molecular Genetics and Biotechnology Laboratory, School of Fisheries, Aquaculture, and Aquatic Sciences, and Program of Cell and Molecular Biosciences, Auburn University, Auburn, Alabama 36849, United States of America.
Ning LiThe Fish Molecular Genetics and Biotechnology Laboratory, School of Fisheries, Aquaculture, and Aquatic Sciences, and Program of Cell and Molecular Biosciences, Auburn University, Auburn, Alabama 36849, United States of America.
Zhanjiang LiuThe Fish Molecular Genetics and Biotechnology Laboratory, School of Fisheries, Aquaculture, and Aquatic Sciences, and Program of Cell and Molecular Biosciences, Auburn University, Auburn, Alabama 36849, United States of America.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Single nucleotide polymorphisms (SNPs) are capable of providing the highest level of genome coverage for genomic and genetic analysis because of their abundance and relatively even distribution in the genome. Such a capacity, however, cannot be achieved without an efficient genotyping platform such as SNP arrays. In this work, we developed a high-density SNP array with 690,662 unique SNPs (herein 690 K array) that were relatively evenly distributed across the entire genome, and covered 98.6% of the reference genome sequence. Here we also report linkage mapping using the 690 K array, which allowed mapping of over 250,000 SNPs on the linkage map, the highest marker density among all the constructed linkage maps. These markers were mapped to 29 linkage groups (LGs) with 30,591 unique marker positions. This linkage map anchored 1,602 scaffolds of the reference genome sequence to LGs, accounting for over 97% of the total genome assembly. A total of 1,007 previously unmapped scaffolds were placed to LGs, allowing validation and in few instances correction of the reference genome sequence assembly. This linkage map should serve as a valuable resource for various genetic and genomic analyses, especially for GWAS and QTL mapping for genes associated with economically important traits.

Indexed as

GenomeAnimalsBase SequenceCatfishesChromosome MappingFemaleGenetic MarkersMalePolymorphism, Single NucleotideReference StandardsReproducibility of ResultsSample SizeSelection, GeneticGenetic Markers

Identifiers

PMID28079141
PMCPMC5228154

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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.