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Application of Cancer Genomics to Solve Unmet Clinical Needs [PDF]

open access: yesGenomics & Informatics, 2013
The large amount of data on cancer genome research has contributed to our understanding of cancer biology. Indeed, the genomics approach has a strong advantage for analyzing multi-factorial and complicated problems, such as cancer.
Se-Hoon Lee   +4 more
doaj   +1 more source

Cancer Genome Landscapes [PDF]

open access: yesScience, 2013
Over the past decade, comprehensive sequencing efforts have revealed the genomic landscapes of common forms of human cancer. For most cancer types, this landscape consists of a small number of “mountains” (genes altered in a high percentage of tumors) and a much larger number of “hills” (genes altered infrequently). To date, these studies have revealed
Bert, Vogelstein   +5 more
openaire   +2 more sources

The cancer genome [PDF]

open access: yesNature, 2009
All cancers arise as a result of changes that have occurred in the DNA sequence of the genomes of cancer cells. Over the past quarter of a century much has been learnt about these mutations and the abnormal genes that operate in human cancers. We are now, however, moving into an era in which it will be possible to obtain the complete DNA sequence of ...
Michael R, Stratton   +2 more
openaire   +2 more sources

Molecular comparison of pure ovarian fibroma with serous benign ovarian tumours

open access: yesBMC Research Notes, 2020
Objective Ovarian fibromas and adenofibromas are rare ovarian tumours. They are benign tumours composed of spindle-like stromal cells (pure fibroma) or a mixture of fibroblast and epithelial components (adenofibroma). We have previously shown that 40% of
Sally M. Hunter   +10 more
doaj   +1 more source

Improved methods for RNAseq-based alternative splicing analysis

open access: yesScientific Reports, 2021
The robust detection of disease-associated splice events from RNAseq data is challenging due to the potential confounding effect of gene expression levels and the often limited number of patients with relevant RNAseq data.
Rebecca F. Halperin   +13 more
doaj   +1 more source

Cancer and genomics [PDF]

open access: yesNature, 2001
Identification of the genes that cause oncogenesis is a central aim of cancer research. We searched the proteins predicted from the draft human genome sequence for paralogues of known tumour suppressor genes, but no novel genes were identified. We then assessed whether it was possible to search directly for oncogenic sequence changes in cancer cells by
P A, Futreal   +5 more
openaire   +2 more sources

Research and Progress of Artificial Intelligence in the Imaging Genomics of Lung Cancer

open access: yesTaiyuan Ligong Daxue xuebao, 2022
Imaging genomics based on artificial intelligence technology has shown great potential in personalized treatment and precision medicine, providing important theoretical basis and technical support for the intelligent diagnosis and prognosis prediction of
Liye JIA   +4 more
doaj   +1 more source

Cancer Genomics [PDF]

open access: yesF1000Research, 2015
Modern cancer genomics has emerged from the combination of the Human Genome Reference, massively parallel sequencing, and the comparison of tumor to normal DNA sequences, revealing novel insights into the cancer genome and its amazing diversity. Recent developments in applying our knowledge of cancer genomics have focused on the utility of these data ...
openaire   +3 more sources

Regulation of 3D Organization and Its Role in Cancer Biology

open access: yesFrontiers in Cell and Developmental Biology, 2022
Three-dimensional (3D) genomics is the frontier field in the post-genomics era, its foremost content is the relationship between chromatin spatial conformation and regulation of gene transcription.
Anghui Peng   +8 more
doaj   +1 more source

Functional Genomic Characterization of Cancer Genomes [PDF]

open access: yesCold Spring Harbor Symposia on Quantitative Biology, 2016
International efforts to sequence cancer genomes now provide an overview of the major genetic alterations that occur in most human cancers. These studies have identified many highly recurrent alterations in specific cancer subtypes but have also identified mutations that occur at lower frequency and unstudied variants of known cancer-associated genes ...
Thomas P, Howard   +7 more
openaire   +2 more sources

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