Evidence map›Paper›PMID 22102592›Full record

ArticleNucleic acids research2012

The Human OligoGenome Resource: a database of oligonucleotide capture probes for resequencing target regions across the human genome.

Daniel E Newburger, Georges Natsoulis, Sue Grimes, John M Bell, Ronald W Davis, Serafim Batzoglou, Hanlee P Ji

Abstract read
In one paragraph

Article in Nucleic acids research, 2012. 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
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.

  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

7 authors.

Daniel E NewburgerBiomedical Informatics Training Program, Division of Oncology, Department of Medicine, Stanford University School of Medicine, Stanford, CA 94305, Stanford Genome Technology Center, Stanford University, Palo Alto and Department of Computer Science, Stanford University, Stanford, CA 94304, USA.
Georges Natsoulis
Sue Grimes
John M Bell
Ronald W Davis
Serafim Batzoglou
Hanlee P Ji

Funding

WHOLE YEAST GENOME TRANSCRIPTIONAL AND FUNCTIONAL GENE MAPS--A FEASIBILITY STUDYP01HG000205 · NHGRI · STANFORD UNIVERSITY · PI HOWE, ROGER THOMAS, JI, HANLEE P · 1990 to 2016
$120.9M
POSTDOCTORAL TRAINING IN MEDICAL INFORMATION SCIENCEST15LM007033 · NLM · STANFORD UNIVERSITY · PI SYLVIA KATINA PLEVRITIS · 1985 to 2026
$25.5M
A Strategy for High Quality Clinical Resequencing of the Human GenomeRC2HG005570 · NHGRI · STANFORD UNIVERSITY · PI DAVIS, RONALD WAYNE · 2009 to 2010
$2.8M
Genetics/microsatellite instability in tumor suppressorsK08CA096879 · NCI · STANFORD UNIVERSITY · PI JI, HANLEE · 2002 to 2007
$614k
Development of Selectors for Cancer Mutation AnalysisR21CA128485 · NCI · STANFORD UNIVERSITY · PI DAVIS, RONALD WAYNE · 2007 to 2008
$434k
Howard Hughes Medical InstituteNCI NIH HHS 5K08CA96879-6NCI NIH HHS R21CA12848NCI NIH HHS R21 CA128485NHGRI NIH HHS 2P01HG000205NHGRI NIH HHS RC2 HG005570NHGRI NIH HHS RC2 HG005570-01NLM NIH HHS T15 LM007033NLM NIH HHS T15-LM007033
6 · The paper itself

Abstract

Recent exponential growth in the throughput of next-generation DNA sequencing platforms has dramatically spurred the use of accessible and scalable targeted resequencing approaches. This includes candidate region diagnostic resequencing and novel variant validation from whole genome or exome sequencing analysis. We have previously demonstrated that selective genomic circularization is a robust in-solution approach for capturing and resequencing thousands of target human genome loci such as exons and regulatory sequences. To facilitate the design and production of customized capture assays for any given region in the human genome, we developed the Human OligoGenome Resource (http://oligogenome.stanford.edu/). This online database contains over 21 million capture oligonucleotide sequences. It enables one to create customized and highly multiplexed resequencing assays of target regions across the human genome and is not restricted to coding regions. In total, this resource provides 92.1% in silico coverage of the human genome. The online server allows researchers to download a complete repository of oligonucleotide probes and design customized capture assays to target multiple regions throughout the human genome. The website has query tools for selecting and evaluating capture oligonucleotides from specified genomic regions.

Indexed as

Databases, Nucleic AcidGenome, HumanSequence Analysis, DNAChromosome MappingHumansMolecular Sequence AnnotationOligonucleotide ProbesOligonucleotide Probes

Identifiers

PMID22102592
PMCPMC3245143

What OpenQuestion holds

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LicenceCC BY-NC
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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.