ArticleNature biotechnology2013
Next-generation sequencing in the clinic.
Article in Nature biotechnology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 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
24 citing papers in PubMed.
- Article
- Nrf2, A Target for Precision Oncology in Cancer Prognosis and Treatment.Journal of cancer prevention · 2023Review
- Article
- Transcription factor network analysis based on single cell RNA-seq identifies that Trichostatin-a reverses docetaxel resistance in prostate Cancer.BMC cancer · 2021Article
- Precision Oncology in Metastatic Uterine Cancer; Croatian First-Year Experience of the Comprehensive Genomic Profiling in Everyday Clinical Practice.Pathology oncology research : POR · 2021Article
- CopyDetective: Detection threshold-aware copy number variant calling in whole-exome sequencing data.GigaScience · 2020Article
- appreci8: a pipeline for precise variant calling integrating 8 tools.Bioinformatics (Oxford, England) · 2018Article
- Comparing the performance of selected variant callers using synthetic data and genome segmentation.BMC bioinformatics · 2018Article
- ToTem: a tool for variant calling pipeline optimization.BMC bioinformatics · 2018Article
- Article
- Personalized and precision medicine: integrating genomics into treatment decisions in gastrointestinal malignancies.Journal of gastrointestinal oncology · 2017Review
- Evaluating Variant Calling Tools for Non-Matched Next-Generation Sequencing Data.Scientific reports · 2017Article
- Versatile ion S5XL sequencer for targeted next generation sequencing of solid tumors in a clinical laboratory.PloS one · 2017Article
- NRAS germline variant G138R and multiple rare somatic mutations on APC in colorectal cancer patients in Taiwan by next generation sequencing.Oncotarget · 2016Article
- VarDict: a novel and versatile variant caller for next-generation sequencing in cancer research.Nucleic acids research · 2016Article
- Article
- The new world of the urinary microbiota in women.American journal of obstetrics and gynecology · 2015Article
- Merkel Cell Carcinoma with a Suppressor of Fused (SUFU) Mutation: Case Report and Potential Therapeutic Implications.Dermatology and therapy · 2015Article
- 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 · 2015Article
- A case study for cloud based high throughput analysis of NGS data using the globus genomics system.Computational and structural biotechnology journal · 2015Article
Corrections and comments
- Comment on
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
PubMed holds no abstract for this paper.
Indexed as
Identifiers
24213773What 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.