Cited by 86Genomics and Phylogenetic StudiesGenome Rearrangement AlgorithmsFractal and DNA sequence analysis

Aligning Multiple Whole Genomes with Mercator and MAVID

Dewey, Colin N.·2007·Methods in Molecular Biology

Abstract

The availability of an increasing number of whole genome sequences presents us with the need for tools to quickly put them into a nucleotide-level multiple alignment. Mercator and MAVID are two programs that can be combined to accomplish this task. Given multiple whole genomes as input, Mercator is first used to construct an orthology map, which is then used to guide nucleotide-level multiple alignments produced by MAVID. These programs are both fast and freely available, allowing researchers to perform genome alignments on a single laptop. This tutorial will guide the researcher through the steps required for whole-genome alignment with Mercator and MAVID.

Integrity signals

Registry

Crossref · 10.1007/978-1-59745-514-5_14

Cites

1 of 1 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • Memory usage determines the size of genomes or datasets that the algorithm can handle at once.

    “Memory usage determines the size of genomes or datasets that the algorithm can handle at once [45].”

Cites

Flagged first, then by citations

Cited by

Sorted by citations

Authors
Dewey, C. N.
Affiliations
University of California, Berkeley (US)
Corresponding author
Dewey, Colin N.
Venue
Methods in Molecular Biology
Publisher
Humana Press
Published
2007
Volume
395
Pages
221-235
ISSN
  • 1064-3745 (ISSN-L)
  • 1940-6029
OpenAlex
W2412439129
Cited by
86
References
1
Citations by year
2024: 1 · 2023: 1 · 2020: 7 · 2019: 4 · 2018: 4 · 2017: 1 · 2016: 6 · 2015: 6 · 2014: 6 · 2013: 9 · 2012: 8
FWCI
9.18
Type
book chapter
Language
en
Open access
closed
Locations
  • Methods in molecular biology (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genome Rearrangement Algorithms
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fractal and DNA sequence analysis
Keywords
whole-genome alignment, Mercator, comparative genomics, orthologs
MeSH terms
Sequence Alignment, Genome, Internet, Databases, Genetic

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review