Evidence map›Paper›PMID 12930977›Full record

ArticleNucleic acids research2003

Parallel gene analysis with allele-specific padlock probes and tag microarrays.

Johan Banér, Anders Isaksson, Erik Waldenström, Jonas Jarvius, Ulf Landegren, Mats Nilsson

Open access · bronzeAbstract read
In one paragraph

Article in Nucleic acids research, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
8.9field-weighted citation impact, top 2% 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

26 citing papers in PubMed, 115 citations in OpenAlex.

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  4. OligoMiner provides a rapid, flexible environment for the design of genome-scale oligonucleotide in situ hybridization probes.Proceedings of the National Academy of Sciences of the United States of America · 2018
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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.

Johan BanérThe Beijer Laboratory, Department of Genetics and Pathology, Rudbeck Laboratory, SE-751 85 Uppsala, Sweden.
Anders Isaksson
Erik Waldenström
Jonas Jarvius
Ulf Landegren
Mats Nilsson

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Parallel, highly specific analysis methods are required to take advantage of the extensive information about DNA sequence variation and of expressed sequences. We present a scalable laboratory technique suitable to analyze numerous target sequences in multiplexed assays. Sets of padlock probes were applied to analyze single nucleotide variation directly in total genomic DNA or cDNA for parallel genotyping or gene expression analysis. All reacted probes were then co-amplified and identified by hybridization to a standard tag oligonucleotide array. The technique was illustrated by analyzing normal and pathogenic variation within the Wilson disease-related ATP7B gene, both at the level of DNA and RNA, using allele-specific padlock probes.

Indexed as

Adenosine TriphosphatasesAllelesCation Transport ProteinsCopper-Transporting ATPasesDNADNA, ComplementaryDNA Mutational AnalysisGenotypeHumansMutationOligonucleotide Array Sequence AnalysisOligonucleotide ProbesPolymorphism, Single NucleotideReproducibility of ResultsSensitivity and SpecificitySequence Analysis, DNAAdenosine TriphosphatasesATP7B protein, humanCation Transport ProteinsCopper-Transporting ATPasesDNADNA, ComplementaryOligonucleotide Probes

Identifiers

PMID12930977
PMCPMC212823
OpenAlexW2111435467

What OpenQuestion holds

Textmetadata
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.