Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Christine Sumner"'
Autor:
Elisabeth Ormandy, Janella C. Schwab, Samantha Suiter, Nicole Green, Janice Oakley, Pamela Osenkowski, Christine Sumner
Publikováno v:
The American Biology Teacher. 84:399-404
Animal dissection is practiced to varying degrees around the world and is particularly prevalent in North America throughout all levels of education. However, a growing number of studies suggest that non-animal teaching methods (NAMs) (e.g., virtual
Autor:
Vaishnavi Panchapakesa, Pingfang Liu, Lynne Apone, Chen Song, Fiona J. Stewart, Eileen T. Dimalanta, Timur Shtatland, Bradley W. Langhorst, Theodore B. Davis, Christine Sumner, Christine Rozzi, Karen Duggan
Publikováno v:
Cancer Research. 79:3528-3528
Next Generation Sequencing (NGS) is rapidly becoming a powerful tool, by providing a high resolution and global view of the cancer genome mainly through whole genome, whole exome and transcriptome sequencing. This knowledge is important to support dr
Autor:
Barton E. Slatko, Theodore B. Davis, Salvatore Russello, Christine L. Chater, Daniela B. Munafo, Fiona J. Stewart, Andrew F. Gardner, Christine Sumner, Deyra N. Rodriguez, John Morlan, Dominick Sinicropi, Kunbin Qu, Bradley W. Langhorst, Eileen T. Dimalanta
Publikováno v:
Current Protocols in Molecular Biology
Ribosomal RNAs (rRNAs) are extremely abundant, often constituting 80% to 90% of total RNA. Since rRNA sequences are often not of interest in genomic RNA sequencing experiments, rRNAs can be removed from the sample before the library preparation step,
Autor:
Christine Rozzi, Theodore B. Davis, Bradley W. Langhorst, Keerthana Krishnan, Joanna Bybee, Eileen T. Dimalanta, John D Murdoch, Vaishnavi Panchapakesa, Timur Shtatland, Lynne Apone, Laurie Mazzola, Christine Sumner, Pingfang Liu, Fiona J. Stewart, Danielle Rivizzigno, Deyra N. Rodriguez, Karen Duggan
Publikováno v:
Cancer Research. 77:5365-5365
The use of Next Generation Sequencing (NGS) data has been instrumental in advancing our understanding of human genetics, identifying the molecular events that contribute to human disease, and supporting drug development targeted towards precision med
Autor:
Keerthana Krishnan, Vaishnavi Panchapakesa, Lynne Apone, Theodore B. Davis, Joanna Bybee, Laurie Mazzola, Eileen T. Dimalanta, Deyra N. Rodriguez, Daniela B. Munafo, Fiona J. Stewart, Karen Duggan, Christine Sumner, Bradley W. Langhorst, Timur Shtatland, Pingfang Liu, Christine Rozzi, Mehmet Karaca, Danielle Rivizzigno, Erbay Yigit
Publikováno v:
Cancer Research. 77:5406-5406
RNA-seq has become the most popular method for transcriptome analysis and is widely used to study gene expression, detect mutations, fusion transcripts, alternative splicing, and post-transcriptional modifications. It is becoming the method of choice
Autor:
Eileen T. Dimalanta, Christine Sumner, Evans C. Thomas, Pingfang Liu, Fiona J. Stewart, Laurence Ettwiller, Lixin Chen, Theodore B. Davis
Publikováno v:
Cancer Research. 76:3628-3628
Targeted cancer therapy based on genomic alterations can be remarkably effective, and has made significant strides with the recent advances in next-generation sequencing (NGS) technology. Although samples of blood and other bodily fluids are being ac
Autor:
Joanna Bybee, Danielle Rivizzigno, Lynne Apone, Laurie Mazzola, Krishnan Keerthana, Eileen T. Dimalanta, Nicole M. Nichols, Pingfang Liu, Vaish Panchapakesa, Theodore B. Davis, Julie F. Menin, Karen Duggan, Fiona J. Stewart, Deyra N. Rodriguez, Christine L. Chater, Christine Sumner, Yanxia Bei, Brad Langhorst
Publikováno v:
Cancer Research. 76:3620-3620
Early detection and diagnosis of cancer substantially increases the likelihood for successful treatment. Tools that aid in detecting and diagnosing cancer early, therefore, have the potential to greatly impact the clinical outcome for cancer patients
Autor:
Theodore B. Davis, Erbay Yigit, Lynne Apone, Christine Sumner, Gregory J. S. Lohman, Daniela B. Munafo, Fiona J. Stewart, Thomas C. Evans, Nicole M. Nichols, Bradley W. Langhorst, Eileen T. Dimalanta, Pingfang Liu, Eric J. Cantor
Publikováno v:
BMC Proceedings, Vol 6, Iss Suppl 6, p P26 (2012)
BMC Proceedings
BMC Proceedings
Next Generation Sequencing (NGS) has significantly impacted human genetics, enabling a comprehensive characterization of the human genome as well as a better understanding of many genomic abnormalities. By delivering massive DNA sequences at unpreced
Autor:
Christine Sumner, Lynne Apone, Theodore B. Davis, Brad Langhorst, Erbay Yigit, Daniela B. Munafo, Fiona J. Stewart, Eileen T. Dimalanta, Ping Liu, Landon Merrill
Publikováno v:
BMC Proceedings, Vol 6, Iss Suppl 6, p P30 (2012)
BMC Proceedings
BMC Proceedings
Background Standard RNA sequencing approaches generally require double-stranded cDNA synthesis, which erases RNA strand information. Synthesis of a randomly primed double-stranded cDNA followed by addition of adaptors for next-generation sequencing l
Autor:
Christine Sumner, Laurence Ettwiller, Eileen T. Dimalanta, Theodore B. Davis, Fiona J. Stewart, Thomas C. Evans, Pingfang Liu, Lixin Chen
Publikováno v:
Cancer Research. 75:4886-4886
Formalin-fixed, paraffin-embedded (FFPE) clinical samples are an invaluable source of information about genetic alterations in human disease, especially cancer. Next generation sequencing is a powerful tool to mine that information. Unfortunately, se