Evidence map›Paper›PMID 23852418›Full record

ArticleCirculation. Cardiovascular genetics2013

Short read (next-generation) sequencing: a tutorial with cardiomyopathy diagnostics as an exemplar.

Jaya Punetha, Eric P Hoffman

Abstract read
In one paragraph

Article in Circulation. Cardiovascular genetics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Artificial intelligence (AI) and big data in cancer and precision oncology.Computational and structural biotechnology journal · 2020
    Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. GermlineNPJ genomic medicine · 2017
    Article
  13. Diagnostic yield of molecular autopsy in patients with sudden arrhythmic death syndrome using targeted exome sequencing.Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology · 2016
    Article
  14. Article
  15. Genetic Variation in Cardiomyopathy and Cardiovascular Disorders.Circulation journal : official journal of the Japanese Circulation Society · 2015
    Review
  16. 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

2 authors.

Jaya PunethaDepartment of Integrative Systems Biology, The George Washington University School of Medicine, Washington, DC, USA.
Eric P Hoffman

Funding

Improved Diagnostic of the Muscular DystrophiesR01NS029525 · NINDS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI HOFFMAN, ERIC P. · 1991 to 2015
$6.5M
NINDS NIH HHS 3R01 NS29525NINDS NIH HHS R01 NS029525
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

High-Throughput Nucleotide SequencingCardiomyopathiesConnectinDNA Copy Number VariationsDystrophinExomeHumansMutationConnectinDystrophinTTN protein, humancardiomyopathiescardiomyopathy, dilatedconnectinexomegeneticshumansMassively-Parallel Sequencing

Identifiers

PMID23852418
PMCPMC4116683

What OpenQuestion holds

Textmetadata
LicenceTDM
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.