Evidence map›Paper›PMID 17705864›Full record

ArticleGenome biology2007

Lessons learned from the initial sequencing of the pig genome: comparative analysis of an 8 Mb region of pig chromosome 17.

Elizabeth A Hart, Mario Caccamo, Jennifer L Harrow, Sean J Humphray, James G R Gilbert, Steve Trevanion, Tim Hubbard, Jane Rogers, Max F Rothschild

Open access · goldAbstract read
In one paragraph

Article in Genome biology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.2field-weighted citation impact, top 11% 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

29 citing papers in PubMed, 47 citations in OpenAlex.

  1. Article
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  6. Review
  7. Intermuscular adipose tissue in metabolic disease.Nature reviews. Endocrinology · 2023
    Review
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  9. Article
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  11. Article
  12. Article
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  17. Large Animal Models: The Key to Translational Discovery in Digestive Disease Research.Cellular and molecular gastroenterology and hepatology · 2016
    Article
  18. Large animal models of cardiovascular disease.Cell biochemistry and function · 2016
    Review
  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

9 authors at 2 institutions in 2 countries.

Elizabeth A HartWellcome Trust Sanger Institute, Wellcome Tust Genome Campus, Hinxton, Cambridge CB10 1SA, UK. eah@sanger.ac.uk
Mario Caccamo
Jennifer L Harrow
Sean J Humphray
James G R Gilbert
Steve Trevanion
Tim Hubbard
Jane Rogers
Max F Rothschild
Wellcome Sanger Institute · GBIowa State University · US

Funding

Biotechnology and Biological Sciences Research Council BBE0116401Wellcome Trust 077198
6 · The paper itself

Abstract

backgroundWe describe here the sequencing, annotation and comparative analysis of an 8 Mb region of pig chromosome 17, which provides a useful test region to assess coverage and quality for the pig genome sequencing project. We report our findings comparing the annotation of draft sequence assembled at different depths of coverage.

resultsWithin this region we annotated 71 loci, of which 53 are orthologous to human known coding genes. When compared to the syntenic regions in human (20q13.13-q13.33) and mouse (chromosome 2, 167.5 Mb-178.3 Mb), this region was found to be highly conserved with respect to gene order. The most notable difference between the three species is the presence of a large expansion of zinc finger coding genes and pseudogenes on mouse chromosome 2 between Edn3 and Phactr3 that is absent from pig and human. All of our annotation has been made publicly available in the Vertebrate Genome Annotation browser, VEGA. We assessed the impact of coverage on sequence assembly across this region and found, as expected, that increased sequence depth resulted in fewer, longer contigs. One-third of our annotated loci could not be fully re-aligned back to the low coverage version of the sequence, principally because the transcripts are fragmented over several contigs.

conclusionWe have demonstrated the considerable advantages of sequencing at increased read depths and discuss the implications that lower coverage sequence may have on subsequent comparative and functional studies, particularly those involving complex loci such as GNAS.

Indexed as

GenomeAnimalsBase SequenceChromosomes, Artificial, BacterialChromosomes, MammalianConserved SequenceCytochrome P-450 Enzyme SystemGene OrderGenome, HumanHumansMiceMolecular ChaperonesMolecular Sequence DataProtein Tyrosine Phosphatase, Non-Receptor Type 1Sequence Analysis, DNASus scrofaCytochrome P-450 Enzyme SystemMolecular ChaperonesprefoldinProtein Tyrosine Phosphatase, Non-Receptor Type 1Vesicular Transport Proteins

Identifiers

PMID17705864
PMCPMC2374978
OpenAlexW2156813592

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.