Evidence map›Paper›PMID 23718862›Full record

ArticleGenome medicine2013

Multiplex target capture with double-stranded DNA probes.

Peidong Shen, Wenyi Wang, Aung-Kyaw Chi, Yu Fan, Ronald W Davis, Curt Scharfe

Registry-linked trialAbstract read
In one paragraph

Article in Genome medicine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02036216 (Detected the Valuable Characteristic Changes Both in Circulating Cell-free DNA and Primary Tumor in the Patients With Hepatocelluar Carcinoma.), which is not on this map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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.

NCT02036216 unknown statusnot on this mapstarted 2014, after this paper: background citation

Detected the Valuable Characteristic Changes Both in Circulating Cell-free DNA and Primary Tumor in the Patients With Hepatocelluar Carcinoma.

TypeobservationalSponsorPeking Union Medical College HospitalRan2014 to 2016Enrolled200ConditionsHepatocellular Carcinoma
3 · Its place in the literature

Who cites it

13 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Transplant Virus Detection Using Multiplex Targeted Sequencing.The journal of applied laboratory medicine · 2018
    Article
  7. Article
  8. Article
  9. Article
  10. The Bottleneck in Genetic Testing.Circulation research · 2015
    Article
  11. Article
  12. Article
  13. 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

6 authors.

Peidong ShenStanford Genome Technology Center, Stanford University, Palo Alto, CA 94304, USA.
Wenyi WangDepartment of Bioinformatics and Computational Biology, UT MD Anderson Cancer Center, Houston, TX 77030, USA.
Aung-Kyaw ChiStanford Genome Technology Center, Stanford University, Palo Alto, CA 94304, USA.
Yu FanDepartment of Bioinformatics and Computational Biology, UT MD Anderson Cancer Center, Houston, TX 77030, USA.
Ronald W DavisStanford Genome Technology Center, Stanford University, Palo Alto, CA 94304, USA.
Curt ScharfeStanford Genome Technology Center, Stanford University, Palo Alto, CA 94304, USA.

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Noninvasive prenatal diagnosis using targeted DNA capture and sequencing.R21HD071446 · NICHD · STANFORD UNIVERSITY · PI DAVIS, RONALD WAYNE · 2011 to 2012
$435k
NCI NIH HHS P30 CA016672NICHD NIH HHS R21 HD071446
6 · The paper itself

Abstract

Target enrichment technologies utilize single-stranded oligonucleotide probes to capture candidate genomic regions from a DNA sample before sequencing. We describe target capture using double-stranded probes, which consist of single-stranded, complementary long padlock probes (cLPPs), each selectively capturing one strand of a genomic target through circularization. Using two probes per target increases sensitivity for variant detection and cLPPs are easily produced by PCR at low cost. Additionally, we introduce an approach for generating capture libraries with uniformly randomized template orientations. This facilitates bidirectional sequencing of both the sense and antisense template strands during one paired-end read, which maximizes target coverage.

Identifiers

PMID23718862
PMCPMC3706973

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Registered trials

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.