Evidence map›Paper›PMID 17202287›Full record

ReviewProceedings of the American Thoracic Society2007

Computational approaches to phenotyping: high-throughput phenomics.

Yves A Lussier, Yang Liu

Open access · greenAbstract readReview
In one paragraph

Review in Proceedings of the American Thoracic Society, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

23 citing papers in PubMed, 61 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Data Science for Child Health.The Journal of pediatrics · 2019
    Review
  6. Article
  7. Review
  8. Identifying and mitigating biases in EHR laboratory tests.Journal of biomedical informatics · 2014
    Article
  9. Article
  10. Systems Epidemiology: What's in a Name?Online journal of public health informatics · 2014
    Article
  11. Identification of homogeneous genetic architecture of multiple genetically correlated traits by block clustering of genome-wide associations.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2011
    Article
  12. Article
  13. Article
  14. Genome-wide pleiotropy of osteoporosis-related phenotypes: the Framingham Study.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2010
    Article
  15. Article
  16. Article
  17. Article
  18. Automated multidimensional phenotypic profiling using large public microarray repositories.Proceedings of the National Academy of Sciences of the United States of America · 2009
    Article
  19. Analysis of AML Genes in Dysregulated Molecular Networks.Summit on translational bioinformatics · 2009
    Article
  20. Article
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

2 authors at 1 institution in 1 country.

Yves A LussierSection of Genetic Medicine, Department of Medicine, University of Chicago,Chicago, Illinois 60637, USA. lussier@uchicago.edu
Yang Liu
University of Chicago · US

Funding

Nation Center: Multi-Scale Study- Cellular Networks(RMI)U54CA121852 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CALIFANO, ANDREA · 2005 to 2015
$37.4M
Capturing and linking genomic and clinical informationR01LM007659 · NLM · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI FRIEDMAN, CAROL · 2003 to 2006
$1.9M
Semantic Approaches to Phenotypic Databases AnalysesK22LM008308 · NLM · UNIVERSITY OF CHICAGO · PI LUSSIER, YVES A · 2004 to 2006
$468k
NCI NIH HHS U54CA121852-01A1NLM NIH HHS 1K22 LM008308-01NLM NIH HHS K22 LM008308NLM NIH HHS R01 LM007659
6 · The paper itself

Abstract

The recent completion of the Human Genome Project has made possible a high-throughput "systems approach" for accelerating the elucidation of molecular underpinnings of human diseases, and subsequent derivation of molecular-based strategies to more effectively prevent, diagnose, and treat these diseases. Although altered phenotypes are among the most reliable manifestations of altered gene functions, research using systematic analysis of phenotype relationships to study human biology is still in its infancy. This article focuses on the emerging field of high-throughput phenotyping (HTP) phenomics research, which aims to capitalize on novel high-throughput computation and informatics technology developments to derive genomewide molecular networks of genotype-phenotype associations, or "phenomic associations." The HTP phenomics research field faces the challenge of technological research and development to generate novel tools in computation and informatics that will allow researchers to amass, access, integrate, organize, and manage phenotypic databases across species and enable genomewide analysis to associate phenotypic information with genomic data at different scales of biology. Key state-of-the-art technological advancements critical for HTP phenomics research are covered in this review. In particular, we highlight the power of computational approaches to conduct large-scale phenomics studies.

Indexed as

Computational BiologyDatabases, GeneticGenomicsPhenotypeHumans

Identifiers

PMID17202287
PMCPMC2647609
OpenAlexW2074557360

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.