cn.FARMS: a latent variable model to detect copy number variations in microarray data with a low false discovery rate (Q33870768)

29 July 2017

cn.FARMS: a latent variable model to detect copy number variations in microarray data with a low false discovery rate (English)

1 reference

29 July 2017

latent variable model

1 reference

9

1 reference

29 July 2017

Günter Klambauer

4

0 references

Djork-Arné Clevert

object named as

Djork-Arné Clevert

1

0 references

Willem Talloen

7

object named as

Willem Talloen

1 reference

29 July 2017

Andreas Mitterecker

2

1 reference

29 July 2017

Andreas Mayr

3

1 reference

29 July 2017

Marianne Tuefferd

5

1 reference

29 July 2017

An De Bondt

6

1 reference

29 July 2017

Hinrich Göhlmann

8

1 reference

29 July 2017

language of work or name

English

0 references

publication date

12 April 2011

1 reference

29 July 2017

Nucleic Acids Research

1 reference

29 July 2017

39

1 reference

29 July 2017

12

1 reference

29 July 2017

e79

1 reference

Creative Commons Attribution-NonCommercial 2.5 Generic

29 July 2017

start time

7 November 2016

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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5 July 2018

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5 July 2018

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5 July 2018

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Integrated detection and population-genetic analysis of SNPs and copy number variation

5 July 2018

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Genotype, haplotype and copy-number variation in worldwide human populations

5 July 2018

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Estimation and assessment of raw copy numbers at the single locus level

5 July 2018

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Copy number variants and common disorders: filling the gaps and exploring complexity in genome-wide association studies

5 July 2018

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

5 July 2018

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I/NI-calls for the exclusion of non-informative genes: a highly effective filtering tool for microarray data

5 July 2018

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Assessment of algorithms for high throughput detection of genomic copy number variation in oligonucleotide microarray data

5 July 2018

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Genome-wide association studies provide new insights into type 2 diabetes aetiology

5 July 2018

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The population genetics of structural variation

5 July 2018

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FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity

5 July 2018

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Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes

5 July 2018

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A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants

5 July 2018

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Global variation in copy number in the human genome

5 July 2018

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A new summarization method for Affymetrix probe level data

5 July 2018

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

5 July 2018

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The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility

5 July 2018

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Analysis of array CGH data: from signal ratio to gain and loss of DNA regions

5 July 2018

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

5 July 2018

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Exploration, normalization, and summaries of high density oligonucleotide array probe level data

5 July 2018

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5 July 2018

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

5 July 2018

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5 July 2018

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5 July 2018

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Approximate Statistical Tests for Comparing Supervised Classification Learning Algorithms.

5 July 2018

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5 July 2018

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Genome-wide, high-resolution detection of copy number, loss of heterozygosity, and genotypes from formalin-fixed, paraffin-embedded tumor tissue using microarrays

5 July 2018

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21 January 2018

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Detection of gene copy number changes in CGH microarrays using a spatially correlated mixture model.

21 January 2018

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A segmental maximum a posteriori approach to genome-wide copy number profiling.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FNAR%2FGKR197

A variational method for learning sparse and overcomplete representations.

21 January 2018

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Genome-wide copy number alterations detection in fresh frozen and matched FFPE samples using SNP 6.0 arrays

21 January 2018

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PubMed

https://pubmed.ncbi.nlm.nih.gov/21486749

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/NAR/GKR197

1 reference

29 July 2017

1 reference

29 July 2017

1 reference