Evidence map›Paper›PMID 15574820›Full record

ArticleGenome research2004

Reconstructing large regions of an ancestral mammalian genome in silico.

Mathieu Blanchette, Eric D Green, Webb Miller, David Haussler

Erratum issuedAbstract 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. An erratum has been issued. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing 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

63 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Complete sequencing of ape genomes.bioRxiv : the preprint server for biology · 2024
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Ancestral Sequence Reconstruction for Exploring Alkaloid Evolution.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Solving the master equation for Indels.BMC bioinformatics · 2017
    Article

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

4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

4 authors.

Mathieu BlanchetteHoward Hughes Medical Institute, University of California, Santa Cruz, California 95064, USA. blanchem@mcb.mcgill.ca
Eric D Green
Webb Miller
David Haussler

Funding

UCSC Center for Genomic Science, and Minority Outreach ProgramP41HG002371 · NHGRI · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI HAUSSLER, DAVID H · 2001 to 2011
$34.8M
Multi-Species Comparative Sequencing of Targeted GenomicZ01HG000196 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI GREEN, ERIC · 2001 to 2008
$19.1M
SOFTWARE FOR ANALYZING BIOSEQUENCE DATAR01HG002238 · NHGRI · PENNSYLVANIA STATE UNIVERSITY-UNIV PARK · PI MILLER, WEBB COLBY · 2000 to 2010
$7.8M
Structural /Functional Analysis of Mammalian ChromosomesZ01HG000060 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI GREEN, ERIC · 1995 to 2008
$6.8M
NHGRI NIH HHS 1P41HG02371NHGRI NIH HHS HG-02238NHGRI NIH HHS P41 HG002371NHGRI NIH HHS R01 HG002238
6 · The paper itself

Abstract

It is believed that most modern mammalian lineages arose from a series of rapid speciation events near the Cretaceous-Tertiary boundary. It is shown that such a phylogeny makes the common ancestral genome sequence an ideal target for reconstruction. Simulations suggest that with methods currently available, we can expect to get 98% of the bases correct in reconstructing megabase-scale euchromatic regions of an eutherian ancestral genome from the genomes of approximately 20 optimally chosen modern mammals. Using actual genomic sequences from 19 extant mammals, we reconstruct 1.1 Mb of ancient genome sequence around the CFTR locus. Detailed examination suggests the reconstruction is accurate and that it allows us to identify features in modern species, such as remnants of ancient transposon insertions, that were not identified by direct analysis. Tracing the predicted evolutionary history of the bases in the reconstructed region, estimates are made of the amount of DNA turnover due to insertion, deletion, and substitution in the different placental mammalian lineages since the common eutherian ancestor, showing considerable variation between lineages. In coming years, such reconstructions may help in identifying and understanding the genetic features common to eutherian mammals and may shed light on the evolution of human or primate-specific traits.

Indexed as

Evolution, MolecularGenetic VariationGenomePhylogenyAnimalsBase SequenceComputer SimulationCystic Fibrosis Transmembrane Conductance RegulatorLikelihood FunctionsMammalsModels, GeneticMolecular Sequence DataSequence AlignmentSequence Analysis, DNACystic Fibrosis Transmembrane Conductance Regulator

Identifiers

PMID15574820
PMCPMC534665

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.