Evidence map›Paper›PMID 23152785›Full record

ArticlePloS one2012

LDx: estimation of linkage disequilibrium from high-throughput pooled resequencing data.

Alison F Feder, Dmitri A Petrov, Alan O Bergland

Abstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed, 1 pooled it
–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

53 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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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

3 authors.

Alison F FederDepartment of Biology, Stanford University, Stanford, California, United States of America. afeder@stanford.edu
Dmitri A Petrov
Alan O Bergland

Funding

Genomic Basis of Vertebrate DiversityP50HG002568 · NHGRI · STANFORD UNIVERSITY · PI KINGSLEY, DAVID M · 2002 to 2011
$29.2M
Genomics of rapid adaptation on seasonal timescales in D. melanogasterR01GM100366 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI SCHMIDT, PAUL · 2012 to 2019
$3.3M
Population Genomics of Adaptive Transposition in DrosophilaR01GM089926 · NIGMS · STANFORD UNIVERSITY · PI PETROV, DMITRI · 2010 to 2013
$969k
Genomics of natural populationsF32GM097837 · NIGMS · STANFORD UNIVERSITY · PI BERGLAND, ALAN OLAV · 2011 to 2013
$148k
NHGRI NIH HHS P50 HG002568NHGRI NIH HHS P50HG002568NIGMS NIH HHS 1R01GM089926NIGMS NIH HHS F32 GM097837NIGMS NIH HHS F32 GM097837-01NIGMS NIH HHS R01 GM089926NIGMS NIH HHS R01 GM100366
6 · The paper itself

Abstract

High-throughput pooled resequencing offers significant potential for whole genome population sequencing. However, its main drawback is the loss of haplotype information. In order to regain some of this information, we present LDx, a computational tool for estimating linkage disequilibrium (LD) from pooled resequencing data. LDx uses an approximate maximum likelihood approach to estimate LD (r(2)) between pairs of SNPs that can be observed within and among single reads. LDx also reports r(2) estimates derived solely from observed genotype counts. We demonstrate that the LDx estimates are highly correlated with r(2) estimated from individually resequenced strains. We discuss the performance of LDx using more stringent quality conditions and infer via simulation the degree to which performance can improve based on read depth. Finally we demonstrate two possible uses of LDx with real and simulated pooled resequencing data. First, we use LDx to infer genomewide patterns of decay of LD with physical distance in D. melanogaster population resequencing data. Second, we demonstrate that r(2) estimates from LDx are capable of distinguishing alternative demographic models representing plausible demographic histories of D. melanogaster.

Indexed as

High-Throughput Nucleotide SequencingLinkage DisequilibriumSequence Analysis, DNASoftwareAlgorithmsAnimalsDrosophila melanogasterGenetic LociHaplotypesInternetPolymorphism, Single NucleotideReproducibility of Results

Identifiers

PMID23152785
PMCPMC3494690

What OpenQuestion holds

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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.