Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Matthew Falkowski"'
Autor:
Malek Faham, Victoria Carlton, Ayca Erbilgin, Paul Hardenbol, Ron Fitzgerald, Francisco Useche, Karen Tran, Martin Moorhead, James S. Ireland, Matthew Falkowski, Thomas D. Willis
Publikováno v:
Human Genetics. 119:75-83
Single nucleotide polymorphisms (SNPs) that lead to non-synonymous changes in proteins may have functional effects and be subject to selection. Hence they are of particular interest in the study of genetic diseases. We have genotyped approximately 28
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6322675d46fef7ea79ca14c6c7625cf7
https://doi.org/10.1007/s00439-005-0105-x
https://doi.org/10.1007/s00439-005-0105-x
Autor:
Maneesh Jain, Hywel B. Jones, Farooq Siddiqui, Martin Moorhead, Carsten Bruckner, Paul Hardenbol, Malek Faham, James S. Ireland, Matthew Falkowski, Thomas D. Willis
Publikováno v:
European journal of human genetics : EJHG. 14(2)
High-throughput genotyping technologies that enable large association studies are already available. Tools for genotype determination starting from raw signal intensities need to be automated, robust, and flexible to provide optimal genotype determin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::343366995ead9fd08d32e15d067c9cfb
https://pubmed.ncbi.nlm.nih.gov/16306880
https://pubmed.ncbi.nlm.nih.gov/16306880
Autor:
Rebecca Pask, Martin Moorhead, Lisa M. Maier, David Clayton, Joanna M. M. Howson, Paul Hardenbol, Deborah J. Smyth, Helen Stevens, John A. Todd, Malek Faham, Thomas D. Willis, Hywel B. Jones, Nigel R. Ovington, Alex C. Lam, Jason D. Cooper, Sarah Nutland, Neil Walker, Luc J. Smink, Matthew Falkowski
Publikováno v:
Nature genetics. 37(11)
The main problems in drawing causal inferences from epidemiological case-control studies are confounding by unmeasured extraneous factors, selection bias and differential misclassification of exposure. In genetics the first of these, in the form of p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a11cec6204b2b19d4249e72291c0f7ee
https://pubmed.ncbi.nlm.nih.gov/16228001
https://pubmed.ncbi.nlm.nih.gov/16228001
Autor:
Thomas D. Willis, Malek Faham, Martin Moorhead, Matthew Falkowski, Maneesh Jain, Carsten Bruckner, Paul Hardenbol, Farooq Siddiqui, James S. Ireland, Hywel B. Jones
Publikováno v:
European Journal of Human Genetics. 14:976-976
Correction to: European Journal of Human Genetics (2006) 14, 207–215. doi: 10.1038/sj.ejhg.5201528 Since publication of the above paper, the authors have identified an error in one of the equations. In the following equation, published on p 208
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f8a359904ef8c9eeffbf87b50f2a9a67
https://doi.org/10.1038/sj.ejhg.5201655
https://doi.org/10.1038/sj.ejhg.5201655
Autor:
Malek Faham, Yuker Wang, Ronald W. Davis, Martin Moorhead, Matthew Falkowski, Thomas D. Willis, Chunnuan Chen, George Karlin-Neumann, Farooq Siddiqui
Publikováno v:
Nucleic Acids Research
Detection of genomic copy number changes has been an important research area, especially in cancer. Several high-throughput technologies have been developed to detect these changes. Features that are important for the utility of technologies assessin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26ef3507173dc917e9203acd48618224
https://doi.org/10.1093/nar/gni177
https://doi.org/10.1093/nar/gni177