ArticleCirculation2012
DNA sequencing: clinical applications of new DNA sequencing technologies.
Article in Circulation, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.
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.
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.
Who cites it
31 citing papers in PubMed.
- Oligonucleotide Selective Detection by Levitated Optomechanics.ACS nanoscience Au · 2026Article
- Addressing data management and analysis challenges in viral genomics: The Swiss HIV cohort study viral next generation sequencing database.PLOS digital health · 2025Article
- Introduction to Special Issue: Genomic Analysis of Common Disease.Current issues in molecular biology · 2025Article
- Genetics of hypertrophic cardiomyopathy: established and emerging implications for clinical practice.European heart journal · 2024Review
- Article
- Article
- The fluorescence amplification strategy based on 3D DNA walker and CRISPR/Cas12a for the rapid detection of BRAF V600E.Analytical sciences : the international journal of the Japan Society for Analytical Chemistry · 2022Article
- A machine learning approach for accurate and real-time DNA sequence identification.BMC genomics · 2021Article
- Re-focusing on Agnathia-Otocephaly complex.Clinical oral investigations · 2021Review
- A newborn screening pilot study using methylation-sensitive high resolution melting on dried blood spots to detect Prader-Willi and Angelman syndromes.Scientific reports · 2020Article
- Review
- ctDNA Detection Based on DNA Clutch Probes and Strand Exchange Mechanism.Frontiers in chemistry · 2018Article
- "Squirrel" Primer-Based PCR Assay for Direct and Targeted Sanger Sequencing of Short Genomic Segments.Journal of biomolecular techniques : JBT · 2017Article
- Cost analysis of whole genome sequencing in German clinical practice.The European journal of health economics : HEPAC : health economics in prevention and care · 2017Article
- Comprehensive genotyping in dyslipidemia: mendelian dyslipidemias caused by rare variants and Mendelian randomization studies using common variants.Journal of human genetics · 2017Review
- Single molecule targeted sequencing for cancer gene mutation detection.Scientific reports · 2016Article
- An assessment of computational methods for estimating purity and clonality using genomic data derived from heterogeneous tumor tissue samples.Briefings in bioinformatics · 2015Review
- A review of study designs and statistical methods for genomic epidemiology studies using next generation sequencing.Frontiers in genetics · 2015Review
- High throughput exome coverage of clinically relevant cardiac genes.BMC medical genomics · 2014Article
- Conventional and genetic talent identification in sports: will recent developments trace talent?Sports medicine (Auckland, N.Z.) · 2014Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
Abstract
PubMed holds no abstract for this paper.
Indexed as
Identifiers
What OpenQuestion holds
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.