Comprehensive comparative homeobox gene annotation in human and mouse

por Wilming, Laurens G., Boychenko, Veronika, Harrow, Jennifer L.
Publicado 2015

Meeting report: a workshop on Best Practices in Genome Annotation

por Madupu, Ramana, Brinkac, Lauren M., Harrow, Jennifer, Wilming, Laurens G., Böhme, Ulrike, Lamesch, Philippe, Hannick, Linda I.
Publicado 2010

Sequencing and characterization of the FVB/NJ mouse genome

por Wong, Kim, Bumpstead, Suzannah, Van Der Weyden, Louise, Reinholdt, Laura G, Wilming, Laurens G, Adams, David J, Keane, Thomas M
Publicado 2012

Dynamic instability of the major urinary protein gene family revealed by genomic and phenotypic comparisons between C57 and 129 strain mice

por Mudge, Jonathan M, Armstrong, Stuart D, McLaren, Karen, Beynon, Robert J, Hurst, Jane L, Nicholson, Christine, Robertson, Duncan H, Wilming, Laurens G, Harrow, Jennifer L
Publicado 2008

The Vertebrate Genome Annotation browser 10 years on

por Harrow, Jennifer L., Steward, Charles A., Frankish, Adam, Gilbert, James G., Gonzalez, Jose M., Loveland, Jane E., Mudge, Jonathan, Sheppard, Dan, Thomas, Mark, Trevanion, Stephen, Wilming, Laurens G.
Publicado 2014

Pseudo–Messenger RNA: Phantoms of the Transcriptome

por Frith, Martin C, Wilming, Laurens G, Forrest, Alistair, Kawaji, Hideya, Tan, Sin Lam, Wahlestedt, Claes, Bajic, Vladimir B, Kai, Chikatoshi, Kawai, Jun, Carninci, Piero, Hayashizaki, Yoshihide, Bailey, Timothy L, Huminiecki, Lukasz
Publicado 2006

Sequencing and comparative analysis of the gorilla MHC genomic sequence

por Wilming, Laurens G., Hart, Elizabeth A., Coggill, Penny C., Horton, Roger, Gilbert, James G. R., Clee, Chris, Jones, Matt, Lloyd, Christine, Palmer, Sophie, Sims, Sarah, Whitehead, Siobhan, Wiley, David, Beck, Stephan, Harrow, Jennifer L.
Publicado 2013

Genetic Analysis of Completely Sequenced Disease-Associated MHC Haplotypes Identifies Shuffling of Segments in Recent Human History

por Traherne, James A, Horton, Roger, Roberts, Anne N, Miretti, Marcos M, Hurles, Matthew E, Stewart, C. Andrew, Ashurst, Jennifer L, Atrazhev, Alexey M, Coggill, Penny, Palmer, Sophie, Almeida, Jeff, Sims, Sarah, Wilming, Laurens G, Rogers, Jane, de Jong, Pieter J., Carrington, Mary, Elliott, John F, Sawcer, Stephen, Todd, John A, Trowsdale, John, Beck, Stephan
Publicado 2006

Discovery of Candidate Disease Genes in ENU–Induced Mouse Mutants by Large-Scale Sequencing, Including a Splice-Site Mutation in Nucleoredoxin

por Boles, Melissa K., Wilkinson, Bonney M., Wilming, Laurens G., Liu, Bin, Probst, Frank J., Harrow, Jennifer, Grafham, Darren, Hentges, Kathryn E., Woodward, Lanette P., Maxwell, Andrea, Mitchell, Karen, Risley, Michael D., Johnson, Randy, Hirschi, Karen, Lupski, James R., Funato, Yosuke, Miki, Hiroaki, Marin-Garcia, Pablo, Matthews, Lucy, Coffey, Alison J., Parker, Anne, Hubbard, Tim J., Rogers, Jane, Bradley, Allan, Adams, David J., Justice, Monica J.
Publicado 2009

Current status and new features of the Consensus Coding Sequence database

por Farrell, Catherine M., O’Leary, Nuala A., Harte, Rachel A., Loveland, Jane E., Wilming, Laurens G., Wallin, Craig, Diekhans, Mark, Barrell, Daniel, Searle, Stephen M. J., Aken, Bronwen, Hiatt, Susan M., Frankish, Adam, Suner, Marie-Marthe, Rajput, Bhanu, Steward, Charles A., Brown, Garth R., Bennett, Ruth, Murphy, Michael, Wu, Wendy, Kay, Mike P., Hart, Jennifer, Rajan, Jeena, Weber, Janet, Snow, Catherine, Riddick, Lillian D., Hunt, Toby, Webb, David, Thomas, Mark, Tamez, Pamela, Rangwala, Sanjida H., McGarvey, Kelly M., Pujar, Shashikant, Shkeda, Andrei, Mudge, Jonathan M., Gonzalez, Jose M., Gilbert, James G. R., Trevanion, Stephen J., Baertsch, Robert, Harrow, Jennifer L., Hubbard, Tim, Ostell, James M., Haussler, David, Pruitt, Kim D.
Publicado 2014