MutaDATABASE: a centralized and standardized DNA variation database.

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

17 citing papers in PubMed.

1. Peter Bauer, Ellen Karges, Gabriela Oprea and Arndt Rolfs.Genetics in medicine : official journal of the American College of Medical Genetics · 2018
   Article
2. A new era in the interpretation of human genomic variation.Genetics in medicine : official journal of the American College of Medical Genetics · 2017
   Article
3. Reporting incidental findings in genomic scale clinical sequencing--a clinical laboratory perspective: a report of the Association for Molecular Pathology.The Journal of molecular diagnostics : JMD · 2015
   Article
4. Cytogenomic Evaluation of Subjects with Syndromic and Nonsyndromic Conotruncal Heart Defects.BioMed research international · 2015
   Article
5. Genomic knowledge sharing: A review of the ethical and legal issues.Applied & translational genomics · 2014
   Review
6. DNA variant databases improve test accuracy and phenotype prediction in Alport syndrome.Pediatric nephrology (Berlin, Germany) · 2014
   Review
7. Human molecular cytogenetics: From cells to nucleotides.Genetics and molecular biology · 2014
   Review
8. Tumor suppressors status in cancer cell line Encyclopedia.Molecular oncology · 2013
   Article
9. Translating next generation sequencing to practice: opportunities and necessary steps.Molecular oncology · 2013
   Review
10. Molecular genetic testing and the future of clinical genomics.Nature reviews. Genetics · 2013
    Review
11. The curation of genetic variants: difficulties and possible solutions.Genomics, proteomics & bioinformatics · 2012
    Review
12. The laboratory-clinician team: a professional call to action to improve communication and collaboration for optimal patient care in chromosomal microarray testing.Journal of genetic counseling · 2012
    Article
13. Patient-controlled encrypted genomic data: an approach to advance clinical genomics.BMC medical genomics · 2012
    Article
14. Consensus: a framework for evaluation of uncertain gene variants in laboratory test reporting.Genome medicine · 2012
    Article
15. Clarity and claims in variation/mutation databasing.Nature biotechnology · 2011
    Article
16. The case for locus-specific databases.Nature reviews. Genetics · 2011
    Article
17. Genetic variations and associated pathophysiology in the management of epilepsy.The application of clinical genetics · 2011
    Article

Corrections and comments

• Commented on by
  Clarity and claims in variation/mutation databasing.2011

Authors and funding

8 authors.

Funding

No grant is acknowledged in the PubMed record.

Abstract

PubMed holds no abstract for this paper.

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