Evidence map›Paper›PMID 10449764›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1999

Sequence-tagged connectors: a sequence approach to mapping and scanning the human genome.

G G Mahairas, J C Wallace, K Smith, S Swartzell, T Holzman, A Keller, R Shaker, J Furlong, J Young, S Zhao and 2 more

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing 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

27 citing papers in PubMed.

  1. Review
  2. Review
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  5. Article
  6. Progress in understanding and sequencing the genome of Brassica rapa.International journal of plant genomics · 2008
    Article
  7. Article
  8. Article
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  13. End-sequence profiling: sequence-based analysis of aberrant genomes.Proceedings of the National Academy of Sciences of the United States of America · 2003
    Article
  14. A 1-Mb resolution radiation hybrid map of the canine genome.Proceedings of the National Academy of Sciences of the United States of America · 2003
    Article
  15. Article
  16. Article
  17. A genetic analysis of chromosome territory looping: diverse roles for distal regulatory elements.Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology · 2003
    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

12 authors.

G G MahairasUniversity of Washington High-Throughput Sequencing Center, 401 Queen Anne Avenue North, Seattle, WA 98109, USA.
J C Wallace
K Smith
S Swartzell
T Holzman
A Keller
R Shaker
J Furlong
J Young
S Zhao
M D Adams
L Hood

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The sequence-tagged connector (STC) strategy proposes to generate sequence tags densely scattered (every 3.3 kilobases) across the human genome by arraying 450,000 bacterial artificial chromosomes (BACs) with randomly cleaved inserts, sequencing both ends of each, and preparing a restriction enzyme fingerprint of each. The STC resource, containing end sequences, fingerprints, and arrayed BACs, creates a map where the interrelationships of the individual BAC clones are resolved through their STCs as overlapping BAC clones are sequenced. Once a seed or initiation BAC clone is sequenced, the minimum overlapping 5' and 3' BAC clones can be identified computationally and sequenced. By reiterating this "sequence-then-map by computer analysis against the STC database" strategy, a minimum tiling path of clones can be sequenced at a rate that is primarily limited by the sequencing throughput of individual genome centers. As of February 1999, we had deposited, together with The Institute for Genomic Research (TIGR), into GenBank 314,000 STCs ( approximately 135 megabases), or 4.5% of human genomic DNA. This genome survey reveals numerous genes, genome-wide repeats, simple sequence repeats (potential genetic markers), and CpG islands (potential gene initiation sites). It also illustrates the power of the STC strategy for creating minimum tiling paths of BAC clones for large-scale genomic sequencing. Because the STC resource permits the easy integration of genetic, physical, gene, and sequence maps for chromosomes, it will be a powerful tool for the initial analysis of the human genome and other complex genomes.

Indexed as

Sequence Tagged SitesChromosome MappingDNA FingerprintingGene LibraryHumans

Identifiers

PMID10449764
PMCPMC22280

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.