Cited by 30Algorithms and Data CompressionGenomics and Phylogenetic StudiesFractal and DNA sequence analysis

The DOI matches its Crossref record; 30 of the 30 references it cites were found in a registry or an index.

Application of a superword array in genome assembly

Open access
Huang, X.·2006·Nucleic Acids Research

Abstract

We introduce a data structure called a superword array for finding quickly matches between DNA sequences. The superword array possesses some desirable features of the lookup table and suffix array. We describe simple algorithms for constructing and using a superword array to find pairs of sequences that share a unique superword. The algorithms are implemented in a genome assembly program called PCAP.REP for computation of overlaps between reads. Experimental results produced by PCAP.REP and PCAP on a whole-genome dataset show that PCAP.REP produced a more accurate and contiguous assembly than PCAP.

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1093/nar/gkj419

Cites

30 of 30 references verified0 citation errors · 0 not checkable

Statistics

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

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?

  • A total of approximately 1.2 million single nucleotide polymorphisms (SNPs) were identified within the 1.84-Gb sequenced female platypus genome using two independent analyses, SSAHA2 and PCAP output.

    “We identified a total of , 1.2 million single nucleotide polymorphisms (SNPs) within the 1.84-Gb sequenced female platypus genomeusing two independent analyses, SSAHA2 (SSAHA: a fast search method for large DNA databases 72 ) and PCAP output 20 (Supplementary Notes 11).”

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

Flagged first, then by citations

Research works printed but not linked: 1

  1. [4]Batzoglou S. Jaffe D. Stanley K. Butler J. Gnerre S. Mauceli E. Berger B. Mesirov J.P. Lander E.S. ARACHNE: a whole-genome shotgun assembler Genome Res. 2002 12 177 189 11779843 PMC155255

Cited by

Sorted by citations

Metadata

Authors
Huang, X.
Affiliations
Iowa State University (US)
Corresponding author
Huang, X.
Venue
Nucleic Acids Research
Published
2006-01-08
Volume
34
Issue
1
Pages
201-205
ISSN
  • 0305-1048 (ISSN-L)
  • 1362-4962
OpenAlex
W2103052607
Cited by
30
References
30
Citations by year
2019: 1 · 2017: 1 · 2016: 1 · 2015: 2 · 2014: 5 · 2012: 1
FWCI
4.56
Type
journal article
Language
en
Open access
Licence
other-oa
Locations
  • Nucleic Acids Research (publishedVersion, other-oa)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
  • Digital Commons@Becker (Washington University School of Medicine) (submittedVersion, other-oa)
  • Iowa State University Digital Repository (Iowa State University) (submittedVersion, other-oa)
Funders
  • Iowa State University
  • National Institutes of Health
  • National Human Genome Research Institute (U54HG003079)
Topics
  • Physical Sciences › Mathematics › Theoretical Computer Science › Algorithms and Data Compression
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fractal and DNA sequence analysis
Keywords
genome assembly, sequence matching, suffix arrays, look-up table, PCAP, whole genome sequencing
MeSH terms
Algorithms, Histoplasma, Genome, Fungal, Computational Biology, Genomics

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