(Q41725200)

Statements

scholarly article

1 reference

Europe PubMed Central

PMC publication ID

8 October 2017

Allele-specific copy number profiling by next-generation DNA sequencing (English)

1 reference

Europe PubMed Central

PMC publication ID

8 October 2017

1 reference

based on heuristic

inferred from title

author name string

Hao Chen

1

1 reference

Europe PubMed Central

PMC publication ID

8 October 2017

John M Bell

2

1 reference

Europe PubMed Central

PMC publication ID

8 October 2017

Nicolas A Zavala

3

1 reference

Europe PubMed Central

PMC publication ID

8 October 2017

Hanlee P Ji

4

1 reference

Europe PubMed Central

PMC publication ID

8 October 2017

Nancy R Zhang

5

1 reference

Europe PubMed Central

PMC publication ID

8 October 2017

publication date

3 December 2014

1 reference

Europe PubMed Central

PMC publication ID

8 October 2017

Nucleic Acids Research

1 reference

Europe PubMed Central

PMC publication ID

8 October 2017

43

1 reference

Europe PubMed Central

PMC publication ID

8 October 2017

4

1 reference

Europe PubMed Central

PMC publication ID

8 October 2017

e23

1 reference

Europe PubMed Central

PMC publication ID

8 October 2017

copyright license

Creative Commons Attribution 4.0 International

7 November 2016

1 reference

April 2022 Public Data File from Crossref

copyright status

0 references

High sensitivity detection and quantitation of DNA copy number and single nucleotide variants with single color droplet digital PCR.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4344483

6 June 2018

Patchwork: allele-specific copy number analysis of whole-genome sequenced tumor tissue.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4344483

6 June 2018

Absolute quantification of somatic DNA alterations in human cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4344483

6 June 2018

Estimation of parent specific DNA copy number in tumors using high-density genotyping arrays

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4344483

6 June 2018

Computational methods for discovering structural variation with next-generation sequencing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4344483

6 June 2018

Segmentation-based detection of allelic imbalance and loss-of-heterozygosity in cancer cells using whole genome SNP arrays

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4344483

6 June 2018

Major copy proportion analysis of tumor samples using SNP arrays

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4344483

6 June 2018

SNP arrays in heterogeneous tissue: highly accurate collection of both germline and somatic genetic information from unpaired single tumor samples.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4344483

6 June 2018

PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4344483

6 June 2018

A modified Bayes information criterion with applications to the analysis of comparative genomic hybridization data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4344483

6 June 2018

QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4344483

6 June 2018

A faster circular binary segmentation algorithm for the analysis of array CGH data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4344483

6 June 2018

Inferring loss-of-heterozygosity from unpaired tumors using high-density oligonucleotide SNP arrays

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4344483

6 June 2018

Allele-specific amplification in cancer revealed by SNP array analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4344483

6 June 2018

A comparison study: applying segmentation to array CGH data for downstream analyses

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4344483

6 June 2018

Comparative analysis of algorithms for identifying amplifications and deletions in array CGH data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4344483

6 June 2018

Circular binary segmentation for the analysis of array-based DNA copy number data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4344483

6 June 2018

dChipSNP: significance curve and clustering of SNP-array-based loss-of-heterozygosity data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4344483

6 June 2018

Identifiers

10.1093/NAR/GKU1252

1 reference

Europe PubMed Central

PMC publication ID

8 October 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

8 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

8 October 2017

ResearchGate publication ID

0 references

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