Evidence map›Paper›PMID 24479665›Full record

ArticleBMC research notes2014

Simulating a population genomics data set using FlowSim.

Ketil Malde

Abstract read
In one paragraph

Article in BMC research notes, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

1 author.

Ketil MaldeInstitute of Marine Research, Nordnesgaten 50, Bergen, Norway. ketil.malde@imr.no.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe field of population genetics use the genetic composition of populations to study the effects of ecological and evolutionary factors, including selection, genetic drift, mating structure, and migration. Until recently, these studies were usually based upon the analysis of relatively few (typically 10-20) DNA markers on samples from multiple populations. In contrast, high-throughput sequencing provides large amounts of data and consequently very high resolution genetic information. Recent technological developments are rapidly making this a cost-effective alternative. In addition, sequencing allows both the direct study of genomic differences between population, and the discovery of single nucleotide polymorphism marker that can be subsequently used in high-throughput genotyping. Much of the analysis in population genetics was developed before large scale sequencing became feasible. Methods often do not take into account the characteristics of the different sequencing technologies, and consequently, may not always be well suited to this kind of data.

resultsAlthough the FlowSim suite of tools originally targeted simulation of de novo 454 genomics data, recent developments and enhancements makes it suitable also for simulating other kinds of data. We examine its application to population genomics, and provide examples and supplementary scripts and utilities to aid in this task.

conclusionsSimulation is an important tool to study and develop methods in many fields, and here we demonstrate how to simulate a high-throughput sequencing dataset for population genomics.

Indexed as

Computer SimulationComputational BiologyGenetics, PopulationGenomicsHigh-Throughput Nucleotide SequencingReproducibility of ResultsSequence Analysis, DNA

Identifiers

PMID24479665
PMCPMC3942619

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LicenceCC BY
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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.