Research Topics
Species | Rong ChenSummaryAffiliation: Stanford University Country: USA Publications
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Detail Information
Publications
Non-synonymous and synonymous coding SNPs show similar likelihood and effect size of human disease associationRong Chen
Department of Pediatrics, Stanford University School of Medicine, Stanford, California, United States of America
PLoS ONE 5:e13574. 2010..Our results suggest that sSNPs are just as likely to be involved in disease mechanisms, so we recommend that sSNPs discovered from GWAS should also be examined with functional studies...
FitSNPs: highly differentially expressed genes are more likely to have variants associated with diseaseRong Chen
Stanford Center for Biomedical Informatics Research, 251 Cmpus Drive, Stanford, CA 94305, USA
Genome Biol 9:R170. 2008..We propose to use the more than 200,000 microarray studies in the Gene Expression Omnibus to systematically prioritize candidate SNPs from GWASs...
GeneChaser: identifying all biological and clinical conditions in which genes of interest are differentially expressedRong Chen
Stanford Center for Biomedical Informatics Research, Department of Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA
BMC Bioinformatics 9:548. 2008....
ProfileChaser: searching microarray repositories based on genome-wide patterns of differential expressionJesse M Engreitz
Division of Systems Medicine, Department of Pediatrics, Stanford University School of Medicine, Stanford, CA 94305, USA
Bioinformatics 27:3317-8. 2011..This analysis identifies statistical links to similar expression experiments from the vast array of publicly available data on diseases, drugs, phenotypes and other experimental conditions...
Compartmental localization and clinical relevance of MICA antibodies after renal transplantationLi Li
Department of Pediatrics, Stanford University, Stanford, CA, USA 2 Department of Pathology, Stanford University, Stanford, CA 94304, USA
Transplantation 89:312-9. 2010..Antibodies (Ab) responses to major and minor human leukocyte antigen loci may impact graft survival after organ transplantation...
Phased whole-genome genetic risk in a family quartet using a major allele reference sequenceFrederick E Dewey
Center for Inherited Cardiovascular Disease, Division of Cardiovascular Medicine, Stanford University, Stanford, California, USA
PLoS Genet 7:e1002280. 2011..These ethnicity-specific, family-based approaches to interpretation of genetic variation are emblematic of the next generation of genetic risk assessment using whole-genome sequencing...
Network-based elucidation of human disease similarities reveals common functional modules enriched for pluripotent drug targetsSilpa Suthram
Stanford Center for Biomedical Informatics Research, Stanford University, Stanford, California, USA
PLoS Comput Biol 6:e1000662. 2010....
Content-based microarray search using differential expression profilesJesse M Engreitz
Department of Bioengineering, Stanford University School of Medicine, CA, USA
BMC Bioinformatics 11:603. 2010....
Ontology-driven indexing of public datasets for translational bioinformaticsNigam H Shah
Centre for Biomedical Informatics, School of Medicine, Stanford University, Stanford, CA 94305, USA
BMC Bioinformatics 10:S1. 2009..The key functionality of this system is to enable users to locate biomedical data resources related to particular ontology concepts...
Identifying compartment-specific non-HLA targets after renal transplantation by integrating transcriptome and "antibodyome" measuresLi Li
Department of Pediatrics, Blood and Marrow Transplantation Division, Stanford University, 300 Pasteur Drive, Stanford, CA 94304, USA
Proc Natl Acad Sci U S A 106:4148-53. 2009..Correlation of the most significant non-HLA antibody responses with transplant health and dysfunction are currently underway...
Clinical assessment incorporating a personal genomeEuan A Ashley
Center for Inherited Cardiovascular Disease, Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA, USA
Lancet 375:1525-35. 2010..The cost of genomic information has fallen steeply, but the clinical translation of genetic risk estimates remains unclear. We aimed to undertake an integrated analysis of a complete human genome in a clinical context...
Performance comparison of whole-genome sequencing platformsHugo Y K Lam
Department of Genetics, Stanford University, Stanford, California, USA
Nat Biotechnol 30:78-82. 2012..Our results have important implications for understanding the accuracy and completeness of the genome sequencing platforms...
Progressive histological damage in renal allografts is associated with expression of innate and adaptive immunity genesMaarten Naesens
Division of Nephrology, Department of Pediatrics, Stanford University School of Medicine, Stanford, California, USA
Kidney Int 80:1364-76. 2011..Thus, measurement of specific immune gene expression in protocol biopsies may be warranted to predict the development of subsequent chronic injury in histologically quiescent grafts and as a means to titrate immunosuppressive therapy...
Personal omics profiling reveals dynamic molecular and medical phenotypesRui Chen
Department of Genetics, Stanford University School of Medicine, Stanford, CA 94305, USA
Cell 148:1293-307. 2012..This study demonstrates that longitudinal iPOP can be used to interpret healthy and diseased states by connecting genomic information with additional dynamic omics activity...
Translational bioinformatics in the cloud: an affordable alternativeJoel T Dudley
Program in Biomedical Informatics, Stanford University School of Medicine, 251 Campus Drive, Stanford, CA 94305, USA
Genome Med 2:51. 2010....
Likelihood ratios for genome medicineAlexander A Morgan
Department of Pediatrics and the Department of Medicine, Stanford University School of Medicine, 251 Campus Drive, MS 5415, Stanford, CA 94305 5479, USA
Genome Med 2:30. 2010..By using well-established methods of evidence based medicine, these very many parallel tests may be combined using likelihood ratios to report a post-test probability of disease for use in patient assessment...
Performance comparison of exome DNA sequencing technologiesMichael J Clark
Department of Genetics, Stanford University School of Medicine, Stanford, CA, USA
Nat Biotechnol 29:908-14. 2011..We also compare exome sequencing and whole genome sequencing (WGS) of the same sample, demonstrating that exome sequencing can detect additional small variants missed by WGS...
Interference of globin genes with biomarker discovery for allograft rejection in peripheral blood samplesLi Li
Pediatrics Department, Stanford University, Stanford, CA, USA
Physiol Genomics 32:190-7. 2008..Similar applications may exist for array-based biomarker discovery for other diseases associated with changes in leukocyte trafficking, activation, or function...
Family history of prostate and breast cancer and the risk of prostate cancer in the PSA eraYen Ching Chen
Department of Medicine, Channing Laboratory, Brigham and Women s Hospital, Harvard Medical School, Boston, Massachusetts 02115, USA
Prostate 68:1582-91. 2008..A family history of prostate cancer (PCa) or breast cancer (BCa) has been associated with the risk of PCa, but the risks were inconsistent in terms of the affected family members, and data in the PSA era are limited...
