Patterns and functional implications of rare germline variants across 12 cancer types
出版年份 2015 全文链接
标题
Patterns and functional implications of rare germline variants across 12 cancer types
作者
关键词
-
出版物
Nature Communications
Volume 6, Issue 1, Pages -
出版商
Springer Nature
发表日期
2015-12-22
DOI
10.1038/ncomms10086
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Multiplatform Analysis of 12 Cancer Types Reveals Molecular Classification within and across Tissues of Origin
- (2014) Katherine A. Hoadley et al. CELL
- Most common ‘sporadic’ cancers have a significant germline genetic component
- (2014) Yi Lu et al. HUMAN MOLECULAR GENETICS
- Realizing the promise of cancer predisposition genes
- (2014) Nazneen Rahman NATURE
- Discovery and saturation analysis of cancer genes across 21 tumour types
- (2014) Michael S. Lawrence et al. NATURE
- Age-related mutations associated with clonal hematopoietic expansion and malignancies
- (2014) Mingchao Xie et al. NATURE MEDICINE
- Integrated analysis of germline and somatic variants in ovarian cancer
- (2014) Krishna L. Kanchi et al. Nature Communications
- ACMG clinical laboratory standards for next-generation sequencing
- (2013) Heidi L. Rehm et al. GENETICS IN MEDICINE
- Validation and Implementation of Targeted Capture and Sequencing for the Detection of Actionable Mutation, Copy Number Variation, and Gene Rearrangement in Clinical Cancer Specimens
- (2013) Colin C. Pritchard et al. JOURNAL OF MOLECULAR DIAGNOSTICS
- Mutational landscape and significance across 12 major cancer types
- (2013) Cyriac Kandoth et al. NATURE
- Development and validation of a clinical cancer genomic profiling test based on massively parallel DNA sequencing
- (2013) Garrett M Frampton et al. NATURE BIOTECHNOLOGY
- Cancer Genome Landscapes
- (2013) B. Vogelstein et al. SCIENCE
- MuSiC: Identifying mutational significance in cancer genomes
- (2012) N. D. Dees et al. GENOME RESEARCH
- VarScan 2: Somatic mutation and copy number alteration discovery in cancer by exome sequencing
- (2012) D. C. Koboldt et al. GENOME RESEARCH
- Comprehensive molecular portraits of human breast tumours
- (2012) Daniel C. Koboldt et al. NATURE
- GWAS Integrator: a bioinformatics tool to explore human genetic associations reported in published genome-wide association studies
- (2011) Wei Yu et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Comparison of statistical tests for disease association with rare variants
- (2011) Saonli Basu et al. GENETIC EPIDEMIOLOGY
- Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing
- (2011) T. Walsh et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Identification of Breast Tumor Mutations in BRCA1 That Abolish Its Function in Homologous DNA Recombination
- (2010) D. J.R. Ransburgh et al. CANCER RESEARCH
- Rare genetic variants and the risk of cancer
- (2010) Walter Bodmer et al. CURRENT OPINION IN GENETICS & DEVELOPMENT
- The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
- (2010) A. McKenna et al. GENOME RESEARCH
- Significant Effect of Polymorphisms inCYP2D6andABCC2on Clinical Outcomes of Adjuvant Tamoxifen Therapy for Breast Cancer Patients
- (2010) Kazuma Kiyotani et al. JOURNAL OF CLINICAL ONCOLOGY
- Allelic Selection of Amplicons in Glioblastoma Revealed by Combining Somatic and Germline Analysis
- (2010) Thomas LaFramboise et al. PLoS Genetics
- Pindel: a pattern growth approach to detect break points of large deletions and medium sized insertions from paired-end short reads
- (2009) K. Ye et al. BIOINFORMATICS
- ATM activates p53 by regulating MDM2 oligomerization and E3 processivity
- (2009) Qian Cheng et al. EMBO JOURNAL
- Four novel germline mutations in the MLH1 and PMS2 mismatch repair genes in patients with hereditary nonpolyposis colorectal cancer
- (2009) Mahdi Montazer Haghighi et al. INTERNATIONAL JOURNAL OF COLORECTAL DISEASE
- PALB2 is an integral component of the BRCA complex required for homologous recombination repair
- (2009) S. M. H. Sy et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- The Fanconi Anemia Protein FANCM Can Promote Branch Migration of Holliday Junctions and Replication Forks
- (2008) Kerstin Gari et al. MOLECULAR CELL
- Oncogenic CARD11 Mutations in Human Diffuse Large B Cell Lymphoma
- (2008) G. Lenz et al. SCIENCE
Add your recorded webinar
Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.
Upload NowBecome a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get Started