Evidence map›Paper›PMID 27633116›Full record

ArticleScientific reports2016

Investigation of rare and low-frequency variants using high-throughput sequencing with pooled DNA samples.

Jingwen Wang, Tiina Skoog, Elisabet Einarsdottir, Tea Kaartokallio, Hannele Laivuori, Anna Grauers, Paul Gerdhem, Marjo Hytönen, Hannes Lohi, Juha Kere and 1 more

Abstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Exome Pool-Seq in neurodevelopmental disorders.European journal of human genetics : EJHG · 2017
    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

11 authors.

Jingwen WangDepartment of Biosciences and Nutrition, Karolinska Institutet, SE-14183 Huddinge, Sweden.
Tiina SkoogDepartment of Biosciences and Nutrition, Karolinska Institutet, SE-14183 Huddinge, Sweden.
Elisabet EinarsdottirDepartment of Biosciences and Nutrition, Karolinska Institutet, SE-14183 Huddinge, Sweden.
Tea KaartokallioMedical and Clinical Genetics, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Hannele LaivuoriMedical and Clinical Genetics, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Anna GrauersDepartment of Orthopedics, Karolinska University Hospital and Department of Clinical Sciences, Intervention and Technology (CLINTEC) Karolinska Institutet, Stockholm, Sweden.
Paul GerdhemDepartment of Orthopedics, Karolinska University Hospital and Department of Clinical Sciences, Intervention and Technology (CLINTEC) Karolinska Institutet, Stockholm, Sweden.
Marjo HytönenDepartment of Veterinary Biosciences, and Research Programs Unit, Molecular Neurology, University of Helsinki and Folkhälsan Research Center, Helsinki, Finland.
Hannes LohiDepartment of Veterinary Biosciences, and Research Programs Unit, Molecular Neurology, University of Helsinki and Folkhälsan Research Center, Helsinki, Finland.
Juha KereDepartment of Biosciences and Nutrition, Karolinska Institutet, SE-14183 Huddinge, Sweden.
Hong JiaoDepartment of Biosciences and Nutrition, Karolinska Institutet, SE-14183 Huddinge, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High-throughput sequencing using pooled DNA samples can facilitate genome-wide studies on rare and low-frequency variants in a large population. Some major questions concerning the pooling sequencing strategy are whether rare and low-frequency variants can be detected reliably, and whether estimated minor allele frequencies (MAFs) can represent the actual values obtained from individually genotyped samples. In this study, we evaluated MAF estimates using three variant detection tools with two sets of pooled whole exome sequencing (WES) and one set of pooled whole genome sequencing (WGS) data. Both GATK and Freebayes displayed high sensitivity, specificity and accuracy when detecting rare or low-frequency variants. For the WGS study, 56% of the low-frequency variants in Illumina array have identical MAFs and 26% have one allele difference between sequencing and individual genotyping data. The MAF estimates from WGS correlated well (r = 0.94) with those from Illumina arrays. The MAFs from the pooled WES data also showed high concordance (r = 0.88) with those from the individual genotyping data. In conclusion, the MAFs estimated from pooled DNA sequencing data reflect the MAFs in individually genotyped samples well. The pooling strategy can thus be a rapid and cost-effective approach for the initial screening in large-scale association studies.

Indexed as

ExomeGene FrequencyGenome, HumanAlgorithmsAllelesAnimalsCompulsive BehaviorDNADog DiseasesDogsExome SequencingFemaleFinlandGenome-Wide Association StudyGenotypeHigh-Throughput Nucleotide SequencingDNA

Identifiers

PMID27633116
PMCPMC5025741

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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.