Výsledky vyhledávání - David Bentley
- Zobrazuji výsledky 1 - 20 z 52
- Přejít na další stránku
-
1
-
2
-
3
Long-Range Comparison of Human and Mouse <i>SCL</i> Loci: Localized Regions of Sensitivity to Restriction Endonucleases Correspond Precisely with Peaks of Conserved Noncoding Seque... Autor Berthold Göttgens, James Gilbert, Linda Barton, Darren Grafham, Jane Rogers, David Bentley, Anthony R. Green
Vydáno 2001Artigo -
4
-
5
-
6
-
7
Transcriptional Regulation of the Stem Cell Leukemia Gene (<i>SCL</i>) — Comparative Analysis of Five Vertebrate SCL Loci Autor Berthold Göttgens, Linda Barton, Michael A. Chapman, Angus M. Sinclair, Bjarne Knudsen, Darren Grafham, James Gilbert, Jane Rogers, David Bentley, Anthony R. Green
Vydáno 2002Carta -
8
Paragraph: a graph-based structural variant genotyper for short-read sequence data Autor Sai Chen, Peter Krusche, Egor Dolzhenko, Rachel M. Sherman, Roman Petrovski, Felix Schlesinger, Melanie Kirsche, David Bentley, Michael C. Schatz, Fritz J. Sedlazeck, Michael A. Eberle
Vydáno 2019Artigo -
9
Massive transcriptional start site analysis of human genes in hypoxia cells Autor Katsuya Tsuchihara, Yutaka Suzuki, Hiroyuki Wakaguri, Takuma Irie, Kousuke Tanimoto, Shin Hashimoto, Kouji Matsushima, Junko Mizushima‐Sugano, Riu Yamashita, Kenta Nakai, David Bentley, Hiroyasu Esumi, Sumio Sugano
Vydáno 2009Artigo -
10
A High-Resolution Linkage-Disequilibrium Map of the Human Major Histocompatibility Complex and First Generation of Tag Single-Nucleotide Polymorphisms Autor Marcos Miretti, Emily C. Walsh, Xiayi Ke, Marcos Delgado, Mark Griffiths, Sarah Hunt, Jonathan J. Morrison, Pamela Whittaker, Eric S. Lander, Lon R. Cardon, David Bentley, John D. Rioux, Stephan Beck, Panos Deloukas
Vydáno 2005Artigo -
11
A reference data set of 5.4 million phased human variants validated by genetic inheritance from sequencing a three-generation 17-member pedigree Autor Michael A. Eberle, Epameinondas Fritzilas, Peter Krusche, Morten Källberg, Benjamin L. Moore, Mitchell A. Bekritsky, Zamin Iqbal, Han‐Yu Chuang, Sean Humphray, Aaron L. Halpern, Semyon Kruglyak, Elliott H. Margulies, Gil McVean, David Bentley
Vydáno 2016Artigo -
12
Spinal muscular atrophy diagnosis and carrier screening from genome sequencing data Autor Xiao Chen, Alba Sanchis‐Juan, Courtney E. French, Andrew J. Connell, Isabelle Delon, Zoya Kingsbury, Aditi Chawla, Aaron L. Halpern, Ryan J. Taft, David Bentley, Matthew E.R. Butchbach, F. Lucy Raymond, Michael A. Eberle
Vydáno 2020Artigo -
13
Chromosome 20 deletions in myeloid malignancies: reduction of the common deleted region, generation of a PAC/BAC contig and identification of candidate genes Autor Anthony J. Bench, Elisabeth P. Nacheva, Tracey L. Hood, Jane L. Holden, Lisa French, S Swanton, Kim M Champion, Juan Li, Pamela Whittaker, George Stavrides, Adrienne Hunt, Brian J.P. Huntly, Lynda J. Campbell, David Bentley, Panos Deloukas, Anthony R. Green
Vydáno 2000Artigo -
14
Monitoring chronic lymphocytic leukemia progression by whole genome sequencing reveals heterogeneous clonal evolution patterns Autor Anna Schuh, Jennifer Becq, Sean Humphray, Adrian Alexa, Adam Burns, Ruth Clifford, Stephan M. Feller, Russell Grocock, Shirley Henderson, Irina Khrebtukova, Zoya Kingsbury, Shujun Luo, David J. McBride, Lisa Murray, Toshi Menju, Adele Timbs, Mark T. Ross, Jenny C. Taylor, David Bentley
Vydáno 2012Artigo -
15
Analysis of Circulating Tumor DNA to Monitor Metastatic Breast Cancer Autor Sarah‐Jane Dawson, Dana W.Y. Tsui, Muhammed Murtaza, Heather Biggs, Oscar M. Rueda, Suet‐Feung Chin, Mark Dunning, Davina Gale, Tim Forshew, Betania Mahler‐Araujo, Sabrina Rajan, Sean Humphray, Jennifer Becq, David Halsall, Matthew Wallis, David Bentley, Carlos Caldas, Nitzan Rosenfeld
Vydáno 2013Artigo -
16
Congenital myasthenic syndromes due to mutations in<i>ALG2</i>and<i>ALG14</i> Autor Judith Cossins, Katsiaryna Belaya, Debbie Hicks, Mustafa A. Salih, Sarah Finlayson, Nicola Carboni, Weiwei Liu, Susan Maxwell, Katarzyna Marta Zoltowska, Golara Torabi Farsani, Steven H. Laval, M.Z. Seidhamed, Peter Donnelly, David Bentley, Simon J. McGowan, Juliane Müller, Jacqueline Palace, Hanns Lochmüller, David Beeson
Vydáno 2013Artigo -
17
Whole genome sequencing provides comprehensive genetic testing in childhood B-cell acute lymphoblastic leukaemia Autor Sarra L. Ryan, John F. Peden, Zoya Kingsbury, Claire Schwab, Terena James, Petri Pölönen, Martina Mijušković, Jenn Becq, Richard Yim, Ruth E. Cranston, Dale J. Hedges, Kathryn G. Roberts, Charles G. Mullighan, Ajay Vora, Lisa J. Russell, Robert Bain, Anthony V. Moorman, David Bentley, Christine J. Harrison, Mark T. Ross
Vydáno 2023Artigo -
18
Integrative genomic analysis of childhood acute lymphoblastic leukaemia lacking a genetic biomarker in the UKALL2003 clinical trial Autor Claire Schwab, Ruth E. Cranston, Sarra L. Ryan, Ellie Butler, Emily Winterman, Zoe Hawking, Matthew Bashton, Amir Enshaei, Lisa J. Russell, Zoya Kingsbury, John F. Peden, Emilio Barretta, J. C. Murray, Jude Gibson, Andrew C. Hinchliffe, Robert Bain, Ajay Vora, David Bentley, Mark T. Ross, Anthony V. Moorman, Christine J. Harrison
Vydáno 2022Artigo -
19
Multifocal clonal evolution characterized using circulating tumour DNA in a case of metastatic breast cancer Autor Muhammed Murtaza, Sarah‐Jane Dawson, Katherine Pogrebniak, Oscar M. Rueda, Elena Provenzano, John W. Grant, Suet‐Feung Chin, Dana W.Y. Tsui, Francesco Marass, Davina Gale, H. Raza Ali, Pankti Shah, Tania Contente‐Cuomo, Hossein Farahani, Karey Shumansky, Zoya Kingsbury, Sean Humphray, David Bentley, Sohrab P. Shah, Matthew Wallis, Nitzan Rosenfeld, Carlos Caldas
Vydáno 2015Artigo -
20
An Enhancer Polymorphism at the Cardiomyocyte Intercalated Disc Protein NOS1AP Locus Is a Major Regulator of the QT Interval Autor Ashish Kapoor, Rajesh B. Sekar, Nancy F. Hansen, Karen Fox-Talbot, Michael P. Morley, Vasyl Pihur, Sumantra Chatterjee, Jeffrey Brandimarto, Christine S. Moravec, Sara L. Pulit, Arne Pfeufer, Jim Mullikin, Mark T. Ross, Eric D. Green, David Bentley, Christopher Newton‐Cheh, Eric Boerwinkle, Gordon F. Tomaselli, Thomas P. Cappola, Dan E. Arking, Marc K. Halushka, Aravinda Chakravarti
Vydáno 2014Artigo
Vyhledávací nástroje:
Související témata
Biology
Genetics
Gene
Genome
Computational biology
Medicine
Genotype
Internal medicine
Mutation
Single-nucleotide polymorphism
Whole genome sequencing
Cancer
DNA sequencing
Human genome
Cancer research
Haplotype
1000 Genomes Project
Allele
Bioinformatics
Computer science
Population
Reference genome
Evolutionary biology
Gene expression
Genetic variation
Genotyping
Sequence (biology)
Chromosome
DNA
Exome sequencing