Evidence map›Paper›PMID 12096187›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2002

A deletion-generator compound element allows deletion saturation analysis for genomewide phenotypic annotation.

François Huet, Jeffrey T Lu, Kyl V Myrick, L Ryan Baugh, Madeline A Crosby, William M Gelbart

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing 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

27 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

François HuetDepartment of Molecular and Cellular Biology, Harvard University, 16 Divinity Avenue, Cambridge, MA 02138, USA.
Jeffrey T Lu
Kyl V Myrick
L Ryan Baugh
Madeline A Crosby
William M Gelbart

Funding

PATTERN FORMATION AND GENE ORGANIZATION IN DROSOPHILAR37GM028669 · NIGMS · HARVARD UNIVERSITY · PI GELBART, WILLIAM MARTIN · 1995 to 2004
$2.5M
NIGMS NIH HHS 5 R37 GM28669NIGMS NIH HHS R37 GM028669
6 · The paper itself

Abstract

With the available eukaryotic genome sequences, there are predictions of thousands of previously uncharacterized genes without known function or available mutational variant. Thus, there is an urgent need for efficient genetic tools for genomewide phenotypic analysis. Here we describe such a tool: a deletion-generator technology that exploits properties of a double transposable element to produce molecularly defined deletions at high density and with high efficiency. This double element, called P[wHy], is composed of a "deleter" element hobo, bracketed by two genetic markers and inserted into a "carrier" P element. We have used this P[wHy] element in Drosophila melanogaster to generate sets of nested deletions of sufficient coverage to discriminate among every transcription unit within 60 kb of the starting insertion site. Because these two types of mobile elements, carrier and deleter, can be found in other species, our strategy should be applicable to phenotypic analysis in a variety of model organisms.

Indexed as

Chromosome MappingGene DeletionGenomeSequence DeletionAnimalsDNA ReplicationDrosophila melanogasterMolecular Sequence DataPhenotype

Identifiers

PMID12096187
PMCPMC126605

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.