Evidence map›Paper›PMID 12537574›Full record

ArticleGenome biology2002

Heterochromatic sequences in a Drosophila whole-genome shotgun assembly.

Roger A Hoskins, Christopher D Smith, Joseph W Carlson, A Bernardo Carvalho, Aaron Halpern, Joshua S Kaminker, Cameron Kennedy, Chris J Mungall, Beth A Sullivan, Granger G Sutton and 6 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in Genome biology, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 153 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
153citing papers in PubMed, 1 pooled it
29.6field-weighted citation impact, top 1% 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

153 citing papers in PubMed, 1 synthesis or guideline pooled it, 281 citations in OpenAlex.

  1. Pooled it
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  16. Centromere-Proximal Suppression of Meiotic Crossovers inbioRxiv : the preprint server for biology · 2023
    Article
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  20. Article

93 more citing papers are in PubMed but not listed here.

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

16 authors at 6 institutions in 2 countries.

Roger A HoskinsDepartment of Genome Sciences, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA. rhoskins@lbl.gov
Christopher D Smith
Joseph W Carlson
A Bernardo Carvalho
Aaron Halpern
Joshua S Kaminker
Cameron Kennedy
Chris J Mungall
Beth A Sullivan
Granger G Sutton
Jiro C Yasuhara
Barbara T Wakimoto
Eugene W Myers
Susan E Celniker
Gerald M Rubin
Gary H Karpen
Lawrence Berkeley National Laboratory · USSalk Institute for Biological Studies · USUniversity of California, Berkeley · USUniversity of Washington · USHoward Hughes Medical Institute · USUniversidade Federal do Rio de Janeiro · BR

Funding

TECHNICAL COREP50HG000750 · NHGRI · UNIVERSITY OF CALIFORNIA BERKELEY · PI RUBIN, GERALD M. · 1992 to 2002
$25.5M
The Drosophila Heterochromatin Genome ProjectR01HG000747 · NHGRI · UNIVERSITY OF CALIF-LAWRENC BERKELEY LAB · PI KARPEN, GARY H · 1992 to 2008
$9.3M
NHGRI NIH HHS P50 HG00750NHGRI NIH HHS R01 HG000747NHGRI NIH HHS R01 HG00747
6 · The paper itself

Abstract

backgroundMost eukaryotic genomes include a substantial repeat-rich fraction termed heterochromatin, which is concentrated in centric and telomeric regions. The repetitive nature of heterochromatic sequence makes it difficult to assemble and analyze. To better understand the heterochromatic component of the Drosophila melanogaster genome, we characterized and annotated portions of a whole-genome shotgun sequence assembly.

resultsWGS3, an improved whole-genome shotgun assembly, includes 20.7 Mb of draft-quality sequence not represented in the Release 3 sequence spanning the euchromatin. We annotated this sequence using the methods employed in the re-annotation of the Release 3 euchromatic sequence. This analysis predicted 297 protein-coding genes and six non-protein-coding genes, including known heterochromatic genes, and regions of similarity to known transposable elements. Bacterial artificial chromosome (BAC)-based fluorescence in situ hybridization analysis was used to correlate the genomic sequence with the cytogenetic map in order to refine the genomic definition of the centric heterochromatin; on the basis of our cytological definition, the annotated Release 3 euchromatic sequence extends into the centric heterochromatin on each chromosome arm.

conclusionsWhole-genome shotgun assembly produced a reliable draft-quality sequence of a significant part of the Drosophila heterochromatin. Annotation of this sequence defined the intron-exon structures of 30 known protein-coding genes and 267 protein-coding gene models. The cytogenetic mapping suggests that an additional 150 predicted genes are located in heterochromatin at the base of the Release 3 euchromatic sequence. Our analysis suggests strategies for improving the sequence and annotation of the heterochromatic portions of the Drosophila and other complex genomes.

Indexed as

GenomeAlgorithmsAnimalsContig MappingDatabases, GeneticDNA Transposable ElementsDrosophila melanogasterHeterochromatinSequence Analysis, DNASoftwareDNA Transposable ElementsHeterochromatin

Identifiers

PMID12537574
PMCPMC151187
OpenAlexW2102385769

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.