Evidence map›Paper›PMID 30899333›Full record

ArticleMobile DNA2019

Transposon insertion profiling by sequencing (TIPseq) for mapping LINE-1 insertions in the human genome.

Jared P Steranka, Zuojian Tang, Mark Grivainis, Cheng Ran Lisa Huang, Lindsay M Payer, Fernanda O R Rego, Thiago Luiz Araujo Miller, Pedro A F Galante, Sitharam Ramaswami, Adriana Heguy and 3 more

Abstract read
In one paragraph

Article in Mobile DNA, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Regulation and function of transposable elements in cancer genomes.Cellular and molecular life sciences : CMLS · 2024
    Review
  7. Article
  8. Article
  9. Transposable element polymorphisms improve prediction of complex agronomic traits in rice.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2022
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. The genetics of ductal adenocarcinoma of the pancreas in the year 2020: dramatic progress, but far to go.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2020
    Review
  17. Article
  18. Human transposon insertion profiling by sequencing (TIPseq) to map LINE-1 insertions in single cells.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2020
    Article
  19. Article
  20. 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

13 authors.

Jared P Steranka1Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD 21205 USA.
Zuojian Tang3Department for Biochemistry and Molecular Pharmacology, NYU Langone Health, New York, NY 10016 USA.
Mark Grivainis3Department for Biochemistry and Molecular Pharmacology, NYU Langone Health, New York, NY 10016 USA.
Cheng Ran Lisa Huang2McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205 USA.
Lindsay M Payer1Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD 21205 USA.
Fernanda O R Rego5Centro de Oncologia Molecular, Hospital Sírio-Libanês, São Paulo, Brazil.
Thiago Luiz Araujo Miller5Centro de Oncologia Molecular, Hospital Sírio-Libanês, São Paulo, Brazil.
Pedro A F Galante5Centro de Oncologia Molecular, Hospital Sírio-Libanês, São Paulo, Brazil.
Sitharam Ramaswami7Genome Technology Center, Division of Advanced Research Technologies, NYU Langone Health, New York, NY USA.
Adriana Heguy7Genome Technology Center, Division of Advanced Research Technologies, NYU Langone Health, New York, NY USA.
David Fenyö3Department for Biochemistry and Molecular Pharmacology, NYU Langone Health, New York, NY 10016 USA.
Jef D Boeke4Institute for Systems Genetics, NYU Langone Health, New York, NY 10016 USA.
Kathleen H Burns1Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD 21205 USA.

Funding

Somatic Activation of Retrotransposition: A New Molecular Mechanism of Aging?P01AG051449 · NIA · BROWN UNIVERSITY · PI Jef D BOEKE · 2016 to 2026
$30.4M
Training CoreP50GM107632 · NIGMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI BOEKE, JEF D · 2013 to 2017
$10.0M
Transposon Insertion Polymorphisms in Predispositions to Hematopoietic NeoplasiaR01CA163705 · NCI · JOHNS HOPKINS UNIVERSITY · PI BURNS, KATHLEEN H · 2013 to 2017
$1.7M
Exonizaton of Alu Insertion PolymorphismsR01GM124531 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI BURNS, KATHLEEN H, FLOREA, LILIANA D · 2017 to 2020
$1.3M
NCI NIH HHS R01 CA163705NIA NIH HHS P01 AG051449NIGMS NIH HHS P50 GM107632NIGMS NIH HHS R01 GM124531
6 · The paper itself

Abstract

backgroundTransposable elements make up a significant portion of the human genome. Accurately locating these mobile DNAs is vital to understand their role as a source of structural variation and somatic mutation. To this end, laboratories have developed strategies to selectively amplify or otherwise enrich transposable element insertion sites in genomic DNA.

resultsHere we describe a technique, Transposon Insertion Profiling by sequencing (TIPseq), to map Long INterspersed Element 1 (LINE-1, L1) retrotransposon insertions in the human genome. This method uses vectorette PCR to amplify species-specific L1 (L1PA1) insertion sites followed by paired-end Illumina sequencing. In addition to providing a step-by-step molecular biology protocol, we offer users a guide to our pipeline for data analysis, TIPseqHunter. Our recent studies in pancreatic and ovarian cancer demonstrate the ability of TIPseq to identify invariant (fixed), polymorphic (inherited variants), as well as somatically-acquired L1 insertions that distinguish cancer genomes from a patient's constitutional make-up.

conclusionsTIPseq provides an approach for amplifying evolutionarily young, active transposable element insertion sites from genomic DNA. Our rationale and variations on this protocol may be useful to those mapping L1 and other mobile elements in complex genomes.

Indexed as

LINE-1Next generation sequencingTargeted PCR

Identifiers

PMID30899333
PMCPMC6407172

What OpenQuestion holds

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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.