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  1. Article

    Open Access

    Common and distinct transcriptional signatures of mammalian embryonic lethality

    The Deciphering the Mechanisms of Developmental Disorders programme has analysed the morphological and molecular phenotypes of embryonic and perinatal lethal mouse mutant lines in order to investigate the caus...

    John E. Collins, Richard J. White, Nicole Staudt, Ian M. Sealy in Nature Communications (2019)

  2. Article

    Open Access

    High-throughput and quantitative genome-wide messenger RNA sequencing for molecular phenoty**

    We present a genome-wide messenger RNA (mRNA) sequencing technique that converts small amounts of RNA from many samples into molecular phenotypes. It encompasses all steps from sample preparation to sequence a...

    John E. Collins, Neha Wali, Ian M. Sealy, James A. Morris, Richard J. White in BMC Genomics (2015)

  3. Article

    Correction: Corrigendum: The zebrafish reference genome sequence and its relationship to the human genome

    Nature 496, 498–503 (2013); doi:10.1038/nature12111 In this Letter, five authors were inadvertently omitted: Sharmin Begum and Christine Lloyd from the Wellcome Trust Sanger Institute, and Christa Lanz, Günter...

    Kerstin Howe, Matthew D. Clark, Carlos F. Torroja, James Torrance in Nature (2014)

  4. Article

    Open Access

    The zebrafish reference genome sequence and its relationship to the human genome

    A high-quality sequence assembly of the zebrafish genome reveals the largest gene set of any vertebrate and provides information on key genomic features, and comparison to the human reference genome shows that...

    Kerstin Howe, Matthew D. Clark, Carlos F. Torroja, James Torrance in Nature (2013)

  5. No Access

    Article

    FRT-seq: amplification-free, strand-specific transcriptome sequencing

    By using a reverse transcriptase for the bridge-amplification step on the Illumina Genome Analyzer, RNA conversion to cDNA and sequencing take place directly in the flowcell and yield highly accurate strand-sp...

    Lira Mamanova, Robert M Andrews, Keith D James, Elizabeth M Sheridan in Nature Methods (2010)

  6. Article

    Open Access

    Finishing the finished human chromosome 22 sequence

    Although the human genome sequence was declared complete in 2004, the sequence was interrupted by 341 gaps of which 308 lay in an estimated approximately 28 Mb of euchromatin. While these gaps constitute only ...

    Charlotte G Cole, Owen T McCann, John E Collins, Karen Oliver in Genome Biology (2008)

  7. No Access

    Protocol

    Subcellular Localization of Intracellular Human Proteins by Construction of Tagged Fusion Proteins and Transient Expression in COS-7 Cells

    Identifying the subcellular compartment of a protein is an important step toward assigning protein function. Starting with a clone containing the open reading frame (ORF) of interest, it is possible to attach ...

    John E. Collins in Genomics Protocols (2008)

  8. Article

    Open Access

    A genome annotation-driven approach to cloning the human ORFeome

    We have developed a systematic approach to generating cDNA clones containing full-length open reading frames (ORFs), exploiting knowledge of gene structure from genomic sequence. Each ORF was amplified by PCR ...

    John E Collins, Charmain L Wright, Carol A Edwards, Matthew P Davis in Genome Biology (2004)

  9. No Access

    Protocol

    YAC Library Storage and Transport

    The development of the yeast artificial chromosome (YAC) cloning system (1) and the construction of YAC libraries with large numbers of genome equivalents (26) provided a major impetus to mammalian genome mappin...

    John E. Collins, Sheila Hassock, Ian Dunham in The Nucleic Acid Protocols Handbook (2000)

  10. No Access

    Protocol

    YAC Library Screening

    The storage of yeast artificial chromosome (YAC) libraries in ordered microtiter plates required a new approach to screening for clones containing specific DNA sequences. Screening libraries of some 60,000 clo...

    Charlotte G. Cole, John E. Collins, Ian Dunham in The Nucleic Acid Protocols Handbook (2000)

  11. No Access

    Protocol

    YAC Library Screening

    Yeast artificial chromosome (YAC) libraries stored in microtiter plates are available for screening as either complex PCR pools or hybridization filters generated from YACs gridded at high densities (see ...

    Charlotte G. Cole, John E. Collins, Ian Dunham in The Nucleic Acid Protocols Handbook (2000)

  12. No Access

    Article

    Comparative analyses of the Dominant megacolon-SOX10 genomic interval in mouse and human

    E. Michelle Southard-Smith, John E. Collins, Jane S. Ellison in Mammalian Genome (1999)

  13. No Access

    Article

    Characterization of the human synaptogyrin gene family

    Genomic sequencing was combined with searches of databases for identification of active genes on human chromosome 22. A cosmid from 22q13, located in the telomeric vicinity of the PDGFB (platelet-derived growt...

    Darek Kedra, Hua-Qin Pan, Eyal Seroussi, Ingegerd Fransson in Human Genetics (1998)

  14. No Access

    Protocol

    YAC Library Screening I

    The storage of yeast artificial chromosome (YAC) libraries in ordered microtiter plates required a new approach to screening for clones containing specific DNA sequences. Screening libraries of some 60,000 clo...

    Charlotte G. Cole, John E. Collins, Ian Dunham in YAC Protocols (1996)

  15. No Access

    Protocol

    YAC Library Screening II

    Yeast artificial chromosome (YAC) libraries stored in microtiter plates are available for screening as either complex PCR pools or hybridization filters generated from YACs gridded at high densities (see ...

    Charlotte G. Cole, John E. Collins, Ian Dunham in YAC Protocols (1996)

  16. No Access

    Protocol

    YAC Library Storage and Transport

    The large size of mammalian genomes necessitates the use of cloning vectors that will accommodate genomic DNA inserts of at least several hundred kilobases. The development of the yeast artificial chromosome (...

    John E. Collins, Sheila Hassock, Ian Dunham in YAC Protocols (1996)

  17. No Access

    Article

    Genetic map** of 14 short tandem repeat polymorphisms on human chromosome 22

    We have constructed a linkage map of 14 short tandem repeat polymorphisms (11 with heterozygosity > 70%) on the long arm of human chromosome 22 using 23 non-CEPH pedigrees. Twelve of the markers could be posit...

    Homero P. Vallada, John E. Collins, Ian Dunham, Elisabeth Dawson in Human Genetics (1994)