(Q41821680)

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Detection of Clonal and Subclonal Copy-Number Variants in Cell-Free DNA from Patients with Breast Cancer Using a Massively Multiplexed PCR Methodology

scientific article published on October 2015

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scholarly article

1 reference

Europe PubMed Central

12 October 2017

Detection of Clonal and Subclonal Copy-Number Variants in Cell-Free DNA from Patients with Breast Cancer Using a Massively Multiplexed PCR Methodology (English)

1 reference

Europe PubMed Central

12 October 2017

Tudor Constantin

object named as

Tudor Constantin

3

0 references

Alexander L Simon

object named as

Alexander L Simon

11

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author name string

Eser Kirkizlar

1

1 reference

Europe PubMed Central

12 October 2017

Bernhard Zimmermann

2

1 reference

Europe PubMed Central

12 October 2017

Ryan Swenerton

4

1 reference

Europe PubMed Central

12 October 2017

Bin Hoang

5

1 reference

Europe PubMed Central

12 October 2017

Nicholas Wayham

6

1 reference

Europe PubMed Central

12 October 2017

Joshua E Babiarz

7

1 reference

Europe PubMed Central

12 October 2017

Zachary Demko

8

1 reference

Europe PubMed Central

12 October 2017

Robert J Pelham

9

1 reference

Europe PubMed Central

12 October 2017

Stephanie Kareht

10

1 reference

Europe PubMed Central

12 October 2017

Kristine N Jinnett

12

1 reference

Europe PubMed Central

12 October 2017

Matthew Rabinowitz

13

1 reference

Europe PubMed Central

12 October 2017

Styrmir Sigurjonsson

14

1 reference

Europe PubMed Central

12 October 2017

Matthew Hill

15

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Europe PubMed Central

12 October 2017

publication date

1 October 2015

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Europe PubMed Central

12 October 2017

Translational Oncology

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Europe PubMed Central

12 October 2017

8

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Europe PubMed Central

12 October 2017

5

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Europe PubMed Central

12 October 2017

407-416

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Europe PubMed Central

12 October 2017

Haplotype-resolved genome sequencing: experimental methods and applications

1 reference

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1 reference

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1 reference

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1 reference

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1 reference

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Cancer: evolution within a lifetime

1 reference

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The dynamic range of circulating tumor DNA in metastatic breast cancer

1 reference

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Capturing intra-tumor genetic heterogeneity by de novo mutation profiling of circulating cell-free tumor DNA: a proof-of-principle.

1 reference

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Single-nucleotide polymorphism-based noninvasive prenatal screening in a high-risk and low-risk cohort

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Genomic imbalance in products of conception: single-nucleotide polymorphism chromosomal microarray analysis

1 reference

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1 reference

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Whole-genome haplotyping using long reads and statistical methods

1 reference

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Detection of circulating tumor DNA in early- and late-stage human malignancies

1 reference

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Liquid biopsies: genotyping circulating tumor DNA

1 reference

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Quantitative identification of mutant alleles derived from lung cancer in plasma cell-free DNA via anomaly detection using deep sequencing data

1 reference

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Pan-cancer patterns of somatic copy number alteration

1 reference

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Emerging landscape of oncogenic signatures across human cancers

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Tumour heterogeneity in the clinic

1 reference

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The causes and consequences of genetic heterogeneity in cancer evolution

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Tumour heterogeneity and cancer cell plasticity

1 reference

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6 June 2018

Distinct evolutionary trajectories of primary high-grade serous ovarian cancers revealed through spatial mutational profiling

1 reference

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6 June 2018

SNP-based non-invasive prenatal testing detects sex chromosome aneuploidies with high accuracy

1 reference

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6 June 2018

Circulating tumour cells and cell-free DNA as tools for managing breast cancer

1 reference

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6 June 2018

Validation of targeted sequencing of single-nucleotide polymorphisms for non-invasive prenatal detection of aneuploidy of chromosomes 13, 18, 21, X, and Y.

1 reference

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6 June 2018

Tumor-associated copy number changes in the circulation of patients with prostate cancer identified through whole-genome sequencing.

1 reference

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6 June 2018

Cancer genome landscapes

1 reference

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6 June 2018

Whole-genome haplotyping by dilution, amplification, and sequencing

1 reference

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Analysis of circulating tumor DNA to monitor metastatic breast cancer

1 reference

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Cancer heterogeneity: implications for targeted therapeutics

1 reference

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Detection of chromosomal alterations in the circulation of cancer patients with whole-genome sequencing

1 reference

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Multi-purpose utility of circulating plasma DNA testing in patients with advanced cancers

1 reference

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Functional genomic analysis of chromosomal aberrations in a compendium of 8000 cancer genomes

1 reference

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6 June 2018

Noninvasive prenatal aneuploidy testing of chromosomes 13, 18, 21, X, and Y, using targeted sequencing of polymorphic loci

1 reference

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Intratumor heterogeneity: evolution through space and time

1 reference

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Comprehensive molecular portraits of human breast tumours

1 reference

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Comprehensive molecular characterization of human colon and rectal cancer

1 reference

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The landscape of cancer genes and mutational processes in breast cancer

1 reference

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1 reference

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1 reference

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1 reference

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The landscape of somatic copy-number alteration across human cancers

1 reference

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1 reference

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1 reference

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The cancer genome

1 reference

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Primer3Plus, an enhanced web interface to Primer3

1 reference

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1 reference

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18 August 2018

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1 reference

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18 August 2018

Identifiers

10.1016/J.TRANON.2015.08.004

1 reference

Europe PubMed Central

12 October 2017

1 reference

Europe PubMed Central

12 October 2017

1 reference

Europe PubMed Central

12 October 2017

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