(Q39453584)

12 September 2017

Allele-specific copy number analysis of tumor samples with aneuploidy and tumor heterogeneity (English)

1 reference

12 September 2017

7

Bengt Glimelius

1 reference

12 September 2017

Markus Rasmussen

1

1 reference

12 September 2017

Magnus Sundström

2

1 reference

12 September 2017

Hanna Göransson Kultima

3

1 reference

12 September 2017

Johan Botling

4

1 reference

12 September 2017

Patrick Micke

5

1 reference

12 September 2017

Helgi Birgisson

6

1 reference

12 September 2017

Anders Isaksson

8

1 reference

12 September 2017

24 October 2011

1 reference

12 September 2017

1 reference

12 September 2017

12

1 reference

12 September 2017

10

1 reference

12 September 2017

R108

1 reference

https://scigraph.springernature.com/pub.10.1186/gb-2011-12-10-r108

12 September 2017

0 references

cites work

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=3333778

A statistical approach for detecting genomic aberrations in heterogeneous tumor samples from single nucleotide polymorphism genotyping data

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3333778

Allele-specific copy number analysis of tumors

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3333778

The mutation spectrum revealed by paired genome sequences from a lung cancer patient

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3333778

TumorBoost: normalization of allele-specific tumor copy numbers from a single pair of tumor-normal genotyping microarrays

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3333778

Genome remodelling in a basal-like breast cancer metastasis and xenograft

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3333778

Genome Alteration Print (GAP): a tool to visualize and mine complex cancer genomic profiles obtained by SNP arrays

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3333778

PICNIC: an algorithm to predict absolute allelic copy number variation with microarray cancer data

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3333778

Mutational evolution in a lobular breast tumour profiled at single nucleotide resolution

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3333778

Quantification of normal cell fraction and copy number neutral LOH in clinical lung cancer samples using SNP array data

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3333778

A single-array preprocessing method for estimating full-resolution raw copy numbers from all Affymetrix genotyping arrays including GenomeWideSNP 5 & 6.

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3333778

Predicting drug susceptibility of non-small cell lung cancers based on genetic lesions

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3333778

Genomic copy number determination in cancer cells from single nucleotide polymorphism microarrays based on quantitative genotyping corrected for aneuploidy.

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3333778

Ploidy status and copy number aberrations in primary glioblastomas defined by integrated analysis of allelic ratios, signal ratios and loss of heterozygosity using 500K SNP Mapping Arrays

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3333778

Major copy proportion analysis of tumor samples using SNP arrays

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3333778

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

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3333778

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

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3333778

Chromosome aberrations in solid tumors

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3333778

Chromosome abnormalities in 10 lung cancer cell lines of the NCI-H series analyzed with spectral karyotyping

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3333778

Evidence of gene amplification in the form of double minute chromosomes is frequently observed in lung cancer

15 June 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22023820

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The significance of ploidy and proliferation in the clinical and biological evaluation of bladder tumours: a study of 100 untreated cases

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22023820

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/GB-2011-12-10-R108

1 reference

Dimensions Publication ID

12 September 2017

0 references

1 reference

12 September 2017

PubMed publication ID

22023820

1 reference