Evidence map›Paper›PMID 12824405›Full record

ArticleNucleic acids research2003

DNannotator: Annotation software tool kit for regional genomic sequences.

Chunyu Liu, Tom I Bonner, Tu Nguyen, Jennifer L Lyons, Susan L Christian, Elliot S Gershon

Open access · hybridAbstract readEvaluation Study
In one paragraph

Article in Nucleic acids research, 2003. 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
0.6field-weighted citation impact, top 35% 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, 7 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

6 authors at 1 institution in 1 country.

Chunyu LiuDepartment of Psychiatry, University of Chicago, Chicago, IL, USA. cliu@yoda.bsd.uchicago.edu
Tom I Bonner
Tu Nguyen
Jennifer L Lyons
Susan L Christian
Elliot S Gershon
University of Chicago · US

Funding

Fine Genomic Mapping of 13q32 in Bipolar DisorderR01MH065560 · NIMH · UNIVERSITY OF CHICAGO · PI GERSHON, ELLIOT S · 2002 to 2006
$3.0M
COLLABORATIVE STUDY OF BIPOLAR DISORDERR01MH059535 · NIMH · UNIVERSITY OF CHICAGO · PI GERSHON, ELLIOT S · 1998 to 2007
$1.9M
Identification Of Candidate Genes For Complex DiseasesZ01MH002774 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI BONNER, TOM I · 1999 to 2005
–
NIMH NIH HHS R01 MH059535NIMH NIH HHS R01 MH065560NIMH NIH HHS R01MH59535NIMH NIH HHS R01 MH65560-01
6 · The paper itself

Abstract

Sequence annotation is essential for genomics-based research. Investigators of a specific genomic region who have developed abundant local discoveries such as genes and genetic markers, or have collected annotations from multiple resources, can be overwhelmed by the difficulty in creating local annotation and the complexity of integrating all the annotations. Presenting such integrated data in a form suitable for data mining and high-throughput experimental design is even more daunting. DNannotator, a web application, was designed to perform batch annotation on a sizeable genomic region. It takes annotation source data, such as SNPs, genes, primers, and so on, prepared by the end-user and/or a specified target of genomic DNA, and performs de novo annotation. DNannotator can also robustly migrate existing annotations in GenBank format from one sequence to another. Annotation results are provided in GenBank format and in tab-delimited text, which can be imported and managed in a database or spreadsheet and combined with existing annotation as desired. Graphic viewers, such as Genome Browser or Artemis, can display the annotation results. Reference data (reports on the process) facilitating the user's evaluation of annotation quality are optionally provided. DNannotator can be accessed at http://sky.bsd.uchicago.edu/DNannotator.htm.

Indexed as

SoftwareChromosomes, Human, Pair 13DNA PrimersGenome, HumanGenomicsHumansInternetPolymorphism, Single NucleotideSequence Analysis, DNASequence Tagged SitesUser-Computer InterfaceDNA Primers

Identifiers

PMID12824405
PMCPMC168949
OpenAlexW2137318037

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.