Evidence map›Paper›PMID 29527774›Full record

ArticleAmerican journal of human biology : the official journal of the Human Biology Council2018

A novel pooled-sample multiplex luminex assay for high-throughput measurement of relative telomere length.

Farzana Jasmine, Justin Shinkle, Mekala Sabarinathan, Habibul Ahsan, Brandon L Pierce, Muhammad G Kibriya

Open access · greenAbstract read
In one paragraph

Article in American journal of human biology : the official journal of the Human Biology Council, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.0field-weighted citation impact, top 26% of its field
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

8 citing papers in PubMed, 13 citations in OpenAlex.

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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 at 1 institution in 1 country.

Farzana JasmineDepartment of Public Health Sciences, Biological Sciences Division, University of Chicago, Chicago, Illinois.
Justin ShinkleDepartment of Public Health Sciences, Biological Sciences Division, University of Chicago, Chicago, Illinois.
Mekala SabarinathanDepartment of Public Health Sciences, Biological Sciences Division, University of Chicago, Chicago, Illinois.
Habibul AhsanDepartment of Public Health Sciences, Biological Sciences Division, University of Chicago, Chicago, Illinois.
Brandon L PierceDepartment of Public Health Sciences, Biological Sciences Division, University of Chicago, Chicago, Illinois.
Muhammad G KibriyaDepartment of Public Health Sciences, Biological Sciences Division, University of Chicago, Chicago, Illinois.ORCID 0000-0001-9784-6958
Chicago Department of Public Health · US

Funding

Chemoprevention of arsenic-induced skin cancerR01CA107431 · NCI · UNIVERSITY OF CHICAGO · PI AHSAN, HABIBUL · 2005 to 2014
$17.3M
Arsenic and the Human Genome: susceptibility and response to exposure Supplement 4R35ES028379 · NIEHS · UNIVERSITY OF CHICAGO · PI PIERCE, BRANDON LEE · 2017 to 2024
$5.6M
A Study of Telomeres in an Arsenic-Exposed Bangladesh CohortR01ES020506 · NIEHS · UNIVERSITY OF CHICAGO · PI PIERCE, BRANDON LEE · 2011 to 2015
$1.9M
Telomere length and chromosomal instability across various tissue typesU01HG007601 · NHGRI · UNIVERSITY OF CHICAGO · PI PIERCE, BRANDON LEE · 2014 to 2016
$1.4M
NCI NIH HHS R01 CA107431NHGRI NIH HHS U01 HG007601NIEHS NIH HHS R01 ES020506NIEHS NIH HHS R35 ES028379
6 · The paper itself

Abstract

objectivesRelative telomere length (RTL) is a potential biomarker of aging and risk for chronic disease. Previously, we developed a probe-based RTL assay on Luminex platform, where probes for Telomere (T) and reference gene (R) for a given DNA sample were tested in a single well. Here, we describe a method of pooling multiple samples in one well to increase the throughput and cost-effectiveness.

methodsWe used four different microbeads for the same T-probe and four different microbeads for the same R-probe. Each pair of probe sets were hybridized to DNA in separate plates and then pooled in a single plate for all the subsequent steps. We used DNA samples from 60 independent individuals and repeated in multiple batches to test the precision.

resultsThe precision was good to excellent with Intraclass correlation coefficient (ICC) of 0.908 (95% CI 0.856-0.942). More than 67% of the variation in the RTL could be explained by sample-to-sample variation; less than 0.1% variation was due to batch-to-batch variation and 0.3% variation was explained by bead-to-bead variation. We increased the throughput of RTL Luminex assay from 60 to 240 samples per run. The new assay was validated against the original Luminex assay without pooling (r = 0.79, P = 1.44 × 10

conclusionWe describe a novel high throughput pooled-sample multiplex Luminex assay for RTL with good to excellent precision suitable for large-scale studies.

Indexed as

AdultAgedHigh-Throughput Screening AssaysHumansMiddle AgedReproducibility of ResultsTelomereTelomere ShorteningYoung Adult

Identifiers

PMID29527774
PMCPMC6105449
OpenAlexW2790435333

What OpenQuestion holds

Textmetadata
LicenceTDM
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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.