Normalization of Illumina Infinium whole-genome SNP data improves copy number estimates and allelic intensity ratios (Q33373518)

26 July 2017

title

Normalization of Illumina Infinium whole-genome SNP data improves copy number estimates and allelic intensity ratios (English)

1 reference

Johan Vallon-Christersson

26 July 2017

main subject

whole genome sequencing

1 reference

based on heuristic

inferred from title

author

series ordinal

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26 July 2017

Markus Ringnér

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Mattias Höglund

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Johan Staaf

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26 July 2017

Ake Borg

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26 July 2017

David Lindgren

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26 July 2017

Gunnar Juliusson

series ordinal

1 reference

26 July 2017

Richard Rosenquist

series ordinal

1 reference

26 July 2017

publication date

2 October 2008

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26 July 2017

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26 July 2017

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26 July 2017

page(s)

409

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describes a project that uses

26 July 2017

limma

object named as

limma

2 references

22 June 2022

https://europepmc.org/article/PMC/2572624

based on heuristic

inferred from PubMed Central ID database lookup

CZ Software Mentions: A large dataset of software mentions in the biomedical literature

cites work

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=2572624

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

21 June 2018

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Statistical issues in the analysis of Illumina data

21 June 2018

1 reference

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21 June 2018

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A comparison of DNA copy number profiling platforms

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2572624

Normalization of array-CGH data: influence of copy number imbalances

21 June 2018

1 reference

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

21 June 2018

1 reference

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High-resolution copy number analysis of paraffin-embedded archival tissue using SNP BeadArrays.

21 June 2018

1 reference

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2572624

Exploration, normalization, and genotype calls of high-density oligonucleotide SNP array data

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2572624

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2572624

Spatial normalization of array-CGH data

21 June 2018

1 reference

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A stepwise framework for the normalization of array CGH data

21 June 2018

1 reference

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Experimental comparison and cross-validation of the Affymetrix and Illumina gene expression analysis platforms

21 June 2018

1 reference

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Comparative genomic hybridization

21 June 2018

1 reference

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

21 June 2018

1 reference

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Normalization of cDNA microarray data

21 June 2018

1 reference

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A comparison of normalization methods for high density oligonucleotide array data based on variance and bias

21 June 2018

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Microarray data normalization and transformation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2572624

Normalization for cDNA microarray data: a robust composite method addressing single and multiple slide systematic variation

21 June 2018

1 reference

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Whole-genome genotyping with the single-base extension assay

21 June 2018

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A genome-wide scalable SNP genotyping assay using microarray technology

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2572624

Genotyping over 100,000 SNPs on a pair of oligonucleotide arrays.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2572624

31 October 2018

Aneuploidy and cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2572624

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

31 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/18831757

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1471-2105-9-409

1 reference

journals/bmcbi/StaafVLJRHBR08

26 July 2017

DBLP publication ID

1 reference

DBLP Dataset 2021-01-02

Dimensions Publication ID

28 January 2021

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26 July 2017

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