Results 31 to 40 of about 260,681 (237)

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
Kenneth W. Kinzler   +5 more
openaire   +3 more sources

Association Study between Folate Pathway Gene Single Nucleotide Polymorphisms and Gastric Cancer in Koreans [PDF]

open access: yesGenomics & Informatics, 2012
Gastric cancer is ranked as the most common cancer in Koreans. A recent molecular biological study about the folate pathway gene revealed the correlation with a couple of cancer types.
Jae-Young Yoo   +6 more
doaj   +1 more source

Factor Models for Cancer Signatures [PDF]

open access: yesPhysica A 462 (2016) 527-559, 2016
We present a novel method for extracting cancer signatures by applying statistical risk models (http://ssrn.com/abstract=2732453) from quantitative finance to cancer genome data. Using 1389 whole genome sequenced samples from 14 cancers, we identify an "overall" mode of somatic mutational noise.
arxiv   +1 more source

Genomic Instability in Cancer [PDF]

open access: yesCold Spring Harbor Perspectives in Biology, 2013
One of the fundamental challenges facing the cell is to accurately copy its genetic material to daughter cells. When this process goes awry, genomic instability ensues in which genetic alterations ranging from nucleotide changes to chromosomal translocations and aneuploidy occur.
Tarek Abbas   +3 more
openaire   +3 more sources

Selective therapeutic strategy for p53-deficient cancer by targeting dysregulation in DNA repair

open access: yesCommunications Biology, 2021
Zonneville et al. show that p53 mutant cancers express high levels of the Base Excision Repair (BER) pathway and that deoxyuridine analogues induce DNA damage in p53-mutant TNBC cells.
Justin Zonneville   +10 more
doaj   +1 more source

Genomic imprinting and cancer [PDF]

open access: yesMolecular Pathology, 1998
Genomic imprinting is the phenomenon by which individual alleles of certain genes are expressed differentially according to their parent of origin. The alleles appear to be differentially marked during gametogenesis or during the early part of development. This mark is heritable but reversible from generation to generation, implying a stable epigenetic
P N Schofield, J A Joyce
openaire   +2 more sources

NCI Workshop Report: Clinical and Computational Requirements for Correlating Imaging Phenotypes with Genomics Signatures

open access: yesTranslational Oncology, 2014
The National Cancer Institute (NCI) Cancer Imaging Program organized two related workshops on June 26–27, 2013, entitled “Correlating Imaging Phenotypes with Genomics Signatures Research” and “Scalable Computational Resources as Required for Imaging ...
Rivka Colen   +15 more
doaj   +1 more source

Understanding genomic alterations in cancer genomes using an integrative network approach [PDF]

open access: yes, 2014
In recent years, cancer genome sequencing and other high-throughput studies of cancer genomes have generated many notable discoveries. In this review, Novel genomic alteration mechanisms, such as chromothripsis (chromosomal crisis) and kataegis (mutation storms), and their implications for cancer are discussed.
arxiv   +1 more source

A Clustering Approach to Integrative Analysis of Multiomic Cancer Data [PDF]

open access: yesarXiv, 2022
Rapid technological advances have allowed for molecular profiling across multiple omics domains from a single sample for clinical decision making in many diseases, especially cancer. As tumor development and progression are dynamic biological processes involving composite genomic aberrations, key challenges are to effectively assimilate information ...
arxiv  

Massively parallel digital transcriptional profiling of single cells

open access: yesNature Communications, 2017
Single-cell gene expression analysis is challenging. This work describes a new droplet-based single cell RNA-seq platform capable of processing tens of thousands of cells across 8 independent samples in minutes, and demonstrates cellular subtypes and ...
Grace X. Y. Zheng   +32 more
doaj   +1 more source

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