Evidence map›Paper›PMID 12508121›Full record

ArticleNature2003

The DNA sequence and analysis of human chromosome 14.

Roland Heilig, Ralph Eckenberg, Jean-Louis Petit, Núria Fonknechten, Corinne Da Silva, Laurence Cattolico, Michaël Levy, Valérie Barbe, Véronique de Berardinis, Abel Ureta-Vidal and 89 more

Erratum issuedOpen access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Nature, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
5.8field-weighted citation impact, top 3% 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

34 citing papers in PubMed, 1 synthesis or guideline pooled it, 104 citations in OpenAlex.

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  15. Chromosome duplication (14q) and the genotype phenotype correlation.International journal of fertility & sterility · 2014
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

99 authors at 6 institutions in 2 countries.

Roland HeiligGenoscope-Centre National de Séquençage, 91000, Evry, France. heilig@genoscope.cns.fr
Ralph Eckenberg
Jean-Louis Petit
Núria Fonknechten
Corinne Da Silva
Laurence Cattolico
Michaël Levy
Valérie Barbe
Véronique de Berardinis
Abel Ureta-Vidal
Eric Pelletier
Virginie Vico
Véronique Anthouard
Lee Rowen
Anup Madan
Shizhen Qin
Hui Sun
Hui Du
Kymberlie Pepin
François Artiguenave
Catherine Robert
Corinne Cruaud
Thomas Brüls
Olivier Jaillon
Lucie Friedlander
Gaelle Samson
Philippe Brottier
Susan Cure
Béatrice Ségurens
Franck Anière
Sylvie Samain
Hervé Crespeau
Nissa Abbasi
Nathalie Aiach
Didier Boscus
Rachel Dickhoff
Monica Dors
Ivan Dubois
Cynthia Friedman
Michel Gouyvenoux
Rose James
Anuradha Madan
Barbara Mairey-Estrada
Sophie Mangenot
Nathalie Martins
Manuela Ménard
Sophie Oztas
Amber Ratcliffe
Tristan Shaffer
Barbara Trask
Benoit Vacherie
Chadia Bellemere
Caroline Belser
Marielle Besnard-Gonnet
Delphine Bartol-Mavel
Magali Boutard
Stéphanie Briez-Silla
Stephane Combette
Virginie Dufossé-Laurent
Carolyne Ferron
Christophe Lechaplais
Claudine Louesse
Delphine Muselet
Ghislaine Magdelenat
Emilie Pateau
Emmanuelle Petit
Peggy Sirvain-Trukniewicz
Arnaud Trybou
Nathalie Vega-Czarny
Elodie Bataille
Elodie Bluet
Isabelle Bordelais
Maria Dubois
Corinne Dumont
Thomas Guérin
Sébastien Haffray
Rachid Hammadi
Jacqueline Muanga
Virginie Pellouin
Dominique Robert
Edith Wunderle
Gilbert Gauguet
Alice Roy
Laurent Sainte-Marthe
Jean Verdier
Claude Verdier-Discala
LaDeana Hillier
Lucinda Fulton
John McPherson
Fumihiko Matsuda
Richard Wilson
Claude Scarpelli
Gábor Gyapay
Patrick Wincker
William Saurin
Francis Quétier
Robert Waterston
Leroy Hood
Jean Weissenbach
Genoscope · FRInstitute for Systems Biology · USWashington University in St. Louis · USUniversité d'Évry Val-d'Essonne · FRCentre National de la Recherche Scientifique · FRCentre National de Recherche en Génomique Humaine · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chromosome 14 is one of five acrocentric chromosomes in the human genome. These chromosomes are characterized by a heterochromatic short arm that contains essentially ribosomal RNA genes, and a euchromatic long arm in which most, if not all, of the protein-coding genes are located. The finished sequence of human chromosome 14 comprises 87,410,661 base pairs, representing 100% of its euchromatic portion, in a single continuous segment covering the entire long arm with no gaps. Two loci of crucial importance for the immune system, as well as more than 60 disease genes, have been localized so far on chromosome 14. We identified 1,050 genes and gene fragments, and 393 pseudogenes. On the basis of comparisons with other vertebrate genomes, we estimate that more than 96% of the chromosome 14 genes have been annotated. From an analysis of the CpG island occurrences, we estimate that 70% of these annotated genes are complete at their 5' end.

Indexed as

Physical Chromosome MappingSequence Analysis, DNA5' Untranslated RegionsAnimalsBase CompositionChromosomes, ArtificialChromosomes, Human, Pair 14CpG IslandsDNA, MitochondrialDNA, RibosomalGenesGenomicsHumansImmunityMiceMicrosatellite Repeats5' Untranslated RegionsDNA, MitochondrialDNA, Ribosomal

Identifiers

PMID12508121
OpenAlexW4242932535

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.