Genomic sequencing in acutely ill infants: what will it take to demonstrate clinical value?
Open accessThe claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
No agreement exists on how to assess rapid testing programs or what level of evidence should guide health care system funding.
“there is no consensus on how to evaluate rapid testing programs or what evidentiary threshold should be used for health care system funding.”
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
The citation lists haven’t been fetched yet
References 11 · Cited by 19
- Authors
- Grosse, S. D., & Farnaes, L.
- Affiliations
- Centers for Disease Control and Prevention (US)
- University of California San Diego (US)
- Corresponding author
- Grosse, Scott D.
- Venue
- Genetics in Medicine
- Publisher
- Elsevier BV
- Published
- 2019-02
- Volume
- 21
- Issue
- 2
- Pages
- 269-271
- ISSN
- 1098-3600 (ISSN-L)
- PMC
- PMC6691721
- OpenAlex
- W2887775237
- Cited by
- 19
- References
- 11
- Citations by year
- 2024: 2 · 2023: 2 · 2022: 5 · 2021: 4 · 2020: 4 · 2019: 2
- FWCI
- 1.53
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Genetics in Medicine (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health (CC999999)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genomics and Rare Diseases
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Clinical Biochemistry › Metabolism and Genetic Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Connective tissue disorders research
- Keywords
- infants, neonatal intensive care, pediatric intensive care, clinical value, diagnostic yield, reimbursement, next-generation sequencing, genomic medicine
- MeSH terms
- Chromosome Mapping, Humans, Infant, Medicine, Genomics
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review
