Evidence map›Paper›PMID 15574829›Full record

ArticleGenome research2004

EAnnot: a genome annotation tool using experimental evidence.

Li Ding, Aniko Sabo, Nicolas Berkowicz, Rekha R Meyer, Yoram Shotland, Mark R Johnson, Kymberlie H Pepin, Richard K Wilson, John Spieth

Abstract readComparative Study
In one paragraph

Article in Genome research, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

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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

9 authors.

Li DingGenome Sequencing Center, Washington University School of Medicine, St. Louis, Missouri 63110, USA. lding@watson.wustl.edu
Aniko Sabo
Nicolas Berkowicz
Rekha R Meyer
Yoram Shotland
Mark R Johnson
Kymberlie H Pepin
Richard K Wilson
John Spieth

Funding

SEQUENCING THE HUMAN GENOMEU54HG002042 · NHGRI · WASHINGTON UNIVERSITY · PI WILSON, RICHARD K. · 1999 to 2003
$200.5M
NHGRI NIH HHS HG002042
6 · The paper itself

Abstract

The sequence of any genome becomes most useful for biological experimentation when a complete and accurate gene set is available. Gene prediction programs offer an efficient way to generate an automated gene set. Manual annotation, when performed by experienced annotators, is more accurate and complete than automated annotation. However, it is a laborious and expensive process, and by its nature, introduces a degree of variability not found with automated annotation. EAnnot (Electronic Annotation) is a program originally developed for manually annotating the human genome. It combines the latest bioinformatics tools to extract and analyze a wide range of publicly available data in order to achieve fast and reliable automatic gene prediction and annotation. EAnnot builds gene models based on mRNA, EST, and protein alignments to genomic sequence, attaches supporting evidence to the corresponding genes, identifies pseudogenes, and locates poly(A) sites and signals. Here, we compare manual annotation of human chromosome 6 with annotation performed by EAnnot in order to assess the latter's accuracy. EAnnot can readily be applied to manual annotation of other eukaryotic genomes and can be used to rapidly obtain an automated gene set.

Indexed as

AlgorithmsGenomeBase SequenceChromosomes, Human, Pair 6Computational BiologyGenomicsHumansModels, GeneticSensitivity and SpecificitySequence Alignment

Identifiers

PMID15574829
PMCPMC534675

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.