Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Christine Rozzi"'
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::55ae6db1b3c9544883c9e37af707a83e
https://doi.org/10.1158/1538-7445.am2019-3528
https://doi.org/10.1158/1538-7445.am2019-3528
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e0999222cd6bc128e1a56f7633d6078d
https://doi.org/10.1158/1538-7445.am2017-5365
https://doi.org/10.1158/1538-7445.am2017-5365
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6e8e433444e3082fce45f362b78e2732
https://doi.org/10.1158/1538-7445.am2017-5406
https://doi.org/10.1158/1538-7445.am2017-5406