(Q28752458)

11

0 references

Mats Lambe

9

0 references

Anders Isaksson

Anders Isaksson

14

0 references

Karolina Edlund

2

Karolina Edlund

0 references

Simon Ekman

6

Simon Ekman

0 references

Michael Bergqvist

7

Michael Bergqvist

0 references

Patrick Micke

12

Patrick Micke

0 references

Johan Botling

13

Johan Botling

0 references

author name string

Hanna Göransson

1

0 references

Maria Rydåker

3

0 references

Markus Rasmussen

4

0 references

Johan Winquist

5

0 references

Andrew Thomas

8

0 references

Richard Rosenquist

Creative Commons Attribution 4.0 International

10

0 references

language of work or name

English

0 references

publication date

26 June 2009

0 references

published in

PLOS One

0 references

volume

4

0 references

issue

6

0 references

page(s)

e6057

0 references

copyright license

start time

26 June 2009

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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1 reference

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

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2699026

CARAT: a novel method for allelic detection of DNA copy number changes using high density oligonucleotide arrays

16 March 2017

1 reference

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Allele-specific amplification in cancer revealed by SNP array analysis

16 March 2017

1 reference

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

16 March 2017

1 reference

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A Hidden Markov Model to estimate population mixture and allelic copy-numbers in cancers using Affymetrix SNP arrays

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2699026

SiDCoN: a tool to aid scoring of DNA copy number changes in SNP chip data

3 June 2018

1 reference

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Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2699026

High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2699026

PLASQ: a generalized linear model-based procedure to determine allelic dosage in cancer cells from SNP array data

3 June 2018

1 reference

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Frequent occurrence of uniparental disomy in colorectal cancer

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2699026

Exploring the tumour environment: cancer-associated fibroblasts as targets in cancer therapy

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2699026

Combined genome-wide allelotyping and copy number analysis identify frequent genetic losses without copy number reduction in medulloblastoma

3 June 2018

1 reference

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Laser-assisted cell microdissection using the PALM system

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2699026

A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2699026

Allelic dosage analysis with genotyping microarrays.

3 June 2018

1 reference

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An integrated view of copy number and allelic alterations in the cancer genome using single nucleotide polymorphism arrays

3 June 2018

1 reference

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

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2699026

Screening for copy-number alterations and loss of heterozygosity in chronic lymphocytic leukemia--a comparative study of four differently designed, high resolution microarray platforms

3 June 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19557126

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Coupled analysis of gene expression and chromosomal location

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19557126

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Association between acquired uniparental disomy and homozygous gene mutation in acute myeloid leukemias

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19557126