Evidence map›Paper›PMID 23494241›Full record

ArticleHuman genetics2013

Recursive organizer (ROR): an analytic framework for sequence-based association analysis.

Lue Ping Zhao, Xin Huang

Abstract read
In one paragraph

Article in Human genetics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact, top 93% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
  2. 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 2 institutions in 1 country.

Lue Ping ZhaoDivision of Public Health Sciences, Fred Hutchinson Cancer Research Center, 1100 Fairview Avenue North, Mailstop M2-B500, P.O. Box 19024, Seattle, WA 98109-1024, USA. lzhao@fhcrc.org
Xin Huang
Fred Hutch Cancer Center · USUniversity of Washington · US

Funding

Methods for Correlating SNP Haplotypes with CancerR01CA106320 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI ZHAO, LUE PING · 2004 to 2008
$1.9M
Designs and Methods for Sequence-Based Validation AnalysisR01MH084621 · NIMH · FRED HUTCHINSON CANCER RESEARCH CENTER · PI ZHAO, LUE PING · 2008 to 2012
$1.8M
Methods for Assessing Genetic Association with Time-Varying PhenotypeR01CA119225 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI ZHAO, LUE PING · 2007 to 2010
$1.3M
METHODS/PROGRAMS FOR MAPPING COMPLEX DISEASESR01HG002283 · NHGRI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI ZHAO, LUE PING NA · 2000 to 2002
$1.2M
Haplotype-Based Methods/Software for Analyzing SNP DataR43HG002877 · NHGRI · ENODAR BIOMETRIC CORPORATION · PI ZHAO, LUE PING · 2003 to 2003
$134k
NCI NIH HHS R01 CA106320NCI NIH HHS R01 CA119225NHGRI NIH HHS R01 HG002283NHGRI NIH HHS R43 HG002877NIMH NIH HHS R01 MH084621
6 · The paper itself

Abstract

The advent of next-generation sequencing technologies affords the ability to sequence thousands of subjects cost-effectively, and is revolutionizing the landscape of genetic research. With the evolving genotyping/sequencing technologies, it is not unrealistic to expect that we will soon obtain a pair of diploidic fully phased genome sequences from each subject in the near future. Here, in light of this potential, we propose an analytic framework called, recursive organizer (ROR), which recursively groups sequence variants based upon sequence similarities and their empirical disease associations, into fewer and potentially more interpretable super sequence variants (SSV). As an illustration, we applied ROR to assess an association between HLA-DRB1 and type 1 diabetes (T1D), discovering SSVs of HLA-DRB1 with sequence data from the Wellcome Trust Case Control Consortium. Specifically, ROR reduces 36 observed unique HLA-DRB1 sequences into 8 SSVs that empirically associate with T1D, a fourfold reduction of sequence complexity. Using HLA-DRB1 data from Type 1 Diabetes Genetics Consortium as cases and data from Fred Hutchinson Cancer Research Center as controls, we are able to validate associations of these SSVs with T1D. Further, SSVs consist of nine nucleotides, and each associates with its corresponding amino acids. Detailed examination of these selected amino acids reveals their potential functional roles in protein structures and possible implication to the mechanism of T1D.

Indexed as

AlgorithmsGenome, HumanDiabetes Mellitus, Type 1FemaleGenome-Wide Association StudyHLA-DRB1 ChainsHumansMaleSequence Analysis, DNAHLA-DRB1 Chains

Identifiers

PMID23494241
PMCPMC3683382
OpenAlexW1990407306

What OpenQuestion holds

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Registered trials

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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.