GA4GH: International policies and standards for data sharing across genomic research and healthcare HL Rehm, AJH Page, L Smith, JB Adams, G Alterovitz, LJ Babb, ... Cell Genomics 1 (2), 100029, 2021 | 148 | 2021 |
DNAmod: the DNA modification database AJ Sood*, C Viner*, MM Hoffman Journal of Cheminformatics 11, 30, 2019 | 85 | 2019 |
Splicing mutation analysis reveals previously unrecognized pathways in lymph node-invasive breast cancer SN Dorman, C Viner, PK Rogan Scientific Reports 4, 7063, 2014 | 36 | 2014 |
Modeling methyl-sensitive transcription factor motifs with an expanded epigenetic alphabet C Viner, CA Ishak, J Johnson, NJ Walker, H Shi, MK Sjöberg-Herrera, ... Genome Biology 25, 11, 2024 | 27 | 2024 |
Validation of predicted mRNA splicing mutations using high-throughput transcriptome data C Viner, SN Dorman, BC Shirley, PK Rogan F1000Research 3, 8, 2014 | 18* | 2014 |
Method of validating mRNA splicing mutations in complete transcriptomes PK Rogan, SN Dorman, C Viner, EJ Mucaki US Patent App. 16/448,064, 2019 | 2* | 2019 |
Semi-automated genome annotation using epigenomic data and Segway EG Roberts, M Mendez, C Viner, M Karimzadeh, RCW Chan, R Ancar, ... bioRxiv, 080382, 2016 | 2 | 2016 |
Noncoding mutation analysis reveals previously unrecognized pathways in lymph node-invasive breast cancer SN Dorman, C Viner, BC Shirley, PK Rogan Cancer Research 74 (19 Supplement), 4172, 2014 | 1 | 2014 |
Motif elucidation in ChIP-seq datasets with a knockout control D Denisko*, C Viner*, MM Hoffman Bioinformatics Advances 3 (1), vbad031, 2023 | | 2023 |
Determining the epigenome using DNA alone C Viner, MM Hoffman Nature Methods 12 (3), 191-192, 2015 | | 2015 |
Transcription factor motif discovery and prediction in an expanded epigenetic alphabet C Viner, J Johnson, CE Grant, TL Bailey, WS Noble, MM Hoffman Genome 57 (7), 378-379, 2014 | | 2014 |