Evidence map›Paper›PMID 22065437›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2011

SNP discovery and genotyping for evolutionary genetics using RAD sequencing.

Paul D Etter, Susan Bassham, Paul A Hohenlohe, Eric A Johnson, William A Cresko

Abstract read
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 173 papers.

0numbers the graph read from it
0cells of the map it votes in
173citing 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

173 citing papers in PubMed.

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113 more citing papers are in PubMed but not listed here.

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

5 authors.

Paul D EtterInstitute of Molecular Biology, University of Oregon, Eugene, OR, USA.
Susan Bassham
Paul A Hohenlohe
Eric A Johnson
William A Cresko

Funding

Advancing the Scientific Potential of Transcriptomics in Aquatic ModelsR24OD011199 · OD · UNIVERSITY OF OREGON · PI CRESKO, WILLIAM A, POSTLETHWAIT, JOHN H. · 2012 to 2014
$1.8M
Rapid and cost-efficient genotyping tools for stuides of threespine sticklebackR24GM079486 · NIGMS · UNIVERSITY OF OREGON · PI CRESKO, WILLIAM A · 2007 to 2010
$708k
Advancing the Scientific Potential of Transcriptomics in Aquatic ModelsR24RR032670 · NCRR · UNIVERSITY OF OREGON · PI CRESKO, WILLIAM A, POSTLETHWAIT, JOHN H. · 2011 to 2011
$553k
Mechanisms of dermoskeletal development in fishF32GM078949 · NIGMS · UNIVERSITY OF OREGON · PI BASSHAM, SUSAN LEE · 2007 to 2008
$112k
NCRR NIH HHS R24 RR032670NIGMS NIH HHS 1R24GM079486-01A1NIGMS NIH HHS F32 GM078949NIGMS NIH HHS R24 GM079486NIH HHS R24 OD011199
6 · The paper itself

Abstract

Next-generation sequencing technologies are revolutionizing the field of evolutionary biology, opening the possibility for genetic analysis at scales not previously possible. Research in population genetics, quantitative trait mapping, comparative genomics, and phylogeography that was unthinkable even a few years ago is now possible. More importantly, these next-generation sequencing studies can be performed in organisms for which few genomic resources presently exist. To speed this revolution in evolutionary genetics, we have developed Restriction site Associated DNA (RAD) genotyping, a method that uses Illumina next-generation sequencing to simultaneously discover and score tens to hundreds of thousands of single-nucleotide polymorphism (SNP) markers in hundreds of individuals for minimal investment of resources. In this chapter, we describe the core RAD-seq protocol, which can be modified to suit a diversity of evolutionary genetic questions. In addition, we discuss bioinformatic considerations that arise from unique aspects of next-generation sequencing data as compared to traditional marker-based approaches, and we outline some general analytical approaches for RAD-seq and similar data. Despite considerable progress, the development of analytical tools remains in its infancy, and further work is needed to fully quantify sampling variance and biases in these data types.

Indexed as

Evolution, MolecularBase SequenceDNADNA Restriction EnzymesElectrophoresis, Agar GelGene LibraryGenetics, PopulationGenomeGenotyping TechniquesHumansMolecular Sequence DataPolymerase Chain ReactionPolymorphism, Single NucleotideRestriction MappingRibonucleasesSequence AlignmentDNADNA Restriction EnzymesRibonucleases

Identifiers

PMID22065437
PMCPMC3658458

What OpenQuestion holds

Textmetadata
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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.