Evidence map›Paper›PMID 21233398›Full record

ArticleGenome research2011

Multiplexed shotgun genotyping for rapid and efficient genetic mapping.

Peter Andolfatto, Dan Davison, Deniz Erezyilmaz, Tina T Hu, Joshua Mast, Tomoko Sunayama-Morita, David L Stern

Abstract read
In one paragraph

Article in Genome research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 225 papers.

0numbers the graph read from it
0cells of the map it votes in
225citing 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

225 citing papers in PubMed.

  1. DoEcology and evolution · 2026
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  11. Cis-regulatory evolution ofbioRxiv : the preprint server for biology · 2025
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  13. Conservative evolution of genetic and genomic features inbioRxiv : the preprint server for biology · 2025
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165 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

7 authors.

Peter AndolfattoDepartment of Ecology and Evolutionary Biology, Princeton University, Princeton, NJ 08544, USA. pandolfa@princeton.edu
Dan Davison
Deniz Erezyilmaz
Tina T Hu
Joshua Mast
Tomoko Sunayama-Morita
David L Stern

Funding

Spatial Patterning During DevelopmentP50GM071508 · NIGMS · PRINCETON UNIVERSITY · PI POWELL, SUSAN M · 2004 to 2013
$30.6M
The molecular basis of morphological evolutionR01GM063622 · NIGMS · PRINCETON UNIVERSITY · PI STERN, DAVID L · 2001 to 2010
$2.6M
Howard Hughes Medical InstituteNIGMS NIH HHS GM063622-06A1NIGMS NIH HHS P50 GM071508NIGMS NIH HHS R01 GM063622
6 · The paper itself

Abstract

We present a new approach to genotyping based on multiplexed shotgun sequencing that can identify recombination breakpoints in a large number of individuals simultaneously at a resolution sufficient for most mapping purposes, such as quantitative trait locus (QTL) mapping and mapping of induced mutations. We first describe a simple library construction protocol that uses just 10 ng of genomic DNA per individual and makes the approach accessible to any laboratory with standard molecular biology equipment. Sequencing this library results in a large number of sequence reads widely distributed across the genomes of multiplexed bar-coded individuals. We develop a Hidden Markov Model to estimate ancestry at all genomic locations in all individuals using these data. We demonstrate the utility of the approach by mapping a dominant marker allele in D. simulans to within 105 kb of its true position using 96 F1-backcross individuals genotyped in a single lane on an Illumina Genome Analyzer. We further demonstrate the utility of our method by genetically mapping more than 400 previously unassembled D. simulans contigs to linkage groups and by evaluating the quality of targeted introgression lines. At this level of multiplexing and divergence between strains, our method allows estimation of recombination breakpoints to a median of 38-kb intervals. Our analysis suggests that higher levels of multiplexing and/or use of strains with lower levels of divergence are practicable.

Indexed as

AnimalsChromosome BreakpointsChromosome MappingComputational BiologyDrosophilaFemaleGenes, DominantGenetic MarkersGenotypeMaleMolecular TypingPhenotypeQuantitative Trait LociRecombination, GeneticResearch DesignSequence Analysis, DNAGenetic Markers

Identifiers

PMID21233398
PMCPMC3065708

What OpenQuestion holds

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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.