Evidence map›Paper›PMID 15778292›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2005

An initial strategy for the systematic identification of functional elements in the human genome by low-redundancy comparative sequencing.

Elliott H Margulies, Jade P Vinson, NISC Comparative Sequencing Program, Webb Miller, David B Jaffe, Kerstin Lindblad-Toh, Jean L Chang, Eric D Green, Eric S Lander, James C Mullikin and 1 more

Abstract readComparative Study
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
10.0field-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

59 citing papers in PubMed, 118 citations in OpenAlex.

  1. Article
  2. Revised eutherian gene collections.BMC genomic data · 2022
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Comparative genomic analysis of eutherian kallikrein genes.Molecular genetics and metabolism reports · 2017
    Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Comparative genomic analysis of eutherian ribonuclease A genes.Molecular genetics and genomics : MGG · 2014
    Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

11 authors at 1 institution in 1 country.

Elliott H MarguliesGenome Technology Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Jade P Vinson
NISC Comparative Sequencing Program
Webb Miller
David B Jaffe
Kerstin Lindblad-Toh
Jean L Chang
Eric D Green
Eric S Lander
James C Mullikin
Michele Clamp
Broad Institute · US

Funding

Inter- and Intra-Species Comparative SequencingZIBHG000196 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI THOMAS, JAMES · 2009 to 2025
$177.6M
Multi-Species Comparative Sequencing of Targeted GenomicZ01HG000196 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI GREEN, ERIC · 2001 to 2008
$19.1M
Comparative Genomics Unit ResearchZIAHG200330 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI MULLIKIN, JAMES C · 2009 to 2022
$17.9M
Structural /Functional Analysis of Mammalian ChromosomesZ01HG000060 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI GREEN, ERIC · 1995 to 2008
$6.8M
Structural and Functional Analysis of Mammalian ChromosomesZIAHG000060 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI GREEN, ERIC · 2009 to 2010
$4.3M
Comparative Genomics Unit ResearchZ01HG200330 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI MULLIKIN, JAMES C · 2005 to 2008
$1.6M
6 · The paper itself

Abstract

With the recent completion of a high-quality sequence of the human genome, the challenge is now to understand the functional elements that it encodes. Comparative genomic analysis offers a powerful approach for finding such elements by identifying sequences that have been highly conserved during evolution. Here, we propose an initial strategy for detecting such regions by generating low-redundancy sequence from a collection of 16 eutherian mammals, beyond the 7 for which genome sequence data are already available. We show that such sequence can be accurately aligned to the human genome and used to identify most of the highly conserved regions. Although not a long-term substitute for generating high-quality genomic sequences from many mammalian species, this strategy represents a practical initial approach for rapidly annotating the most evolutionarily conserved sequences in the human genome, providing a key resource for the systematic study of human genome function.

Indexed as

Genome, HumanAnimalsBase SequenceComputational BiologyConserved SequenceGenomicsHumansMammalsPhylogenySequence AlignmentSequence Analysis, DNA

Identifiers

PMID15778292
PMCPMC555705
OpenAlexW2138245520

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.