Evidence map›Paper›PMID 28609193›Full record

ArticleGenetic testing and molecular biomarkers2017

DNA Methylome Profiling on the Infinium HumanMethylation450 Array from Limiting Quantities of Genomic DNA from a Single, Small Archived Bloodspot.

Kripa Asrani, Gary M Shaw, Jasper Rine, Nicholas J Marini

Abstract read
In one paragraph

Article in Genetic testing and molecular biomarkers, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Association of Epigenetic Markers of Aging With Prevalent and Incident Type 2 Diabetes.The journals of gerontology. Series A, Biological sciences and medical sciences · 2025
    Article
  2. Article
  3. Article
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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

4 authors.

Kripa Asrani1 California Institute for Quantitative Biosciences, University of California , Berkeley, California.
Gary M Shaw2 Department of Pediatrics, Stanford University School of Medicine , Stanford, California.
Jasper Rine1 California Institute for Quantitative Biosciences, University of California , Berkeley, California.
Nicholas J Marini1 California Institute for Quantitative Biosciences, University of California , Berkeley, California.

Funding

Impact of Genetic Variation on Folate Metabolsim: Etiology of Neural Tube DefectsR01GM072859 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI RINE, JASPER D · 2007 to 2015
$4.4M
Genetic Risk for Orofacial Clefts in the Folate/Homocysteine PathwayR01HD074695 · NICHD · UNIVERSITY OF CALIFORNIA BERKELEY · PI MARINI, NICHOLAS · 2013 to 2016
$2.0M
NICHD NIH HHS R01 HD074695NIGMS NIH HHS R01 GM072859
6 · The paper itself

Abstract

aimsArchived newborn bloodspots are valuable sample collections for genetic and epigenetic disease research. However, they have often been stored for long periods of time, under less than ideal circumstances, and nucleic acid yields can be low, particularly when samples become limiting. We wished to determine whether the quantity and quality of genomic DNA (gDNA) isolated from a single, surgical bloodspot punch (2 mm dia.) was adequate for accurate and reliable DNA methylome profiling on the Illumina HumanMethylation450 array.

methodsA total of 25-750 ng of archived bloodspot or Jurkat cell gDNA were bisulfite converted and analyzed on the array without any additional DNA amplification steps. Methylation profiles were assessed for call rate, call confidence (detection p-value), and reproducibility.

resultsUsing 25 ng gDNA from either Jurkat cells or dried bloodspots, array-wide call rates (∼99.9%) and detection p-values (99.9% with p < 5 × 10

conclusionsTwenty-five nanograms of gDNA, isolated from a single, surgical punch (2 mm dia.) of an archived newborn bloodspot, generate a genome-wide methylation profile on the Illumina HumanMethylation450 array that is robust, reproducible, and suitable for differential methylation studies.

Indexed as

CpG IslandsDNADNA FingerprintingDNA MethylationEpigenesis, GeneticEpigenomicsHumansInfant, NewbornNucleic Acid Amplification TechniquesOligonucleotide Array Sequence AnalysisPolymorphism, Single NucleotideReproducibility of ResultsSpecimen HandlingDNAbloodspotDNA methylationepigenetics

Identifiers

PMID28609193
PMCPMC5568181

What OpenQuestion holds

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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.