(Q33840267)

29 July 2017

Comparing genotyping algorithms for Illumina's Infinium whole-genome SNP BeadChips (English)

1 reference

29 July 2017

0 references

0 references

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whole genome sequencing

1 reference

Benilton S Carvalho

3

0 references

Matthew E Ritchie

object named as

Matthew E Ritchie

series ordinal

1

0 references

Matthew A. Brown

1 reference

ORCID Public Data File 2021

Rafael Irizarry

series ordinal

5

object named as

Rafael A Irizarry

1 reference

29 July 2017

Ruijie Liu

2

1 reference

PubMed ID

21385424

29 July 2017

Australia and New Zealand Multiple Sclerosis Genetics Consortium (ANZgene)

series ordinal

4

1 reference

29 July 2017

8 March 2011

1 reference

29 July 2017

1 reference

29 July 2017

12

1 reference

29 July 2017

68

1 reference

Creative Commons Attribution 2.0 Generic

29 July 2017

start time

8 March 2011

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

1 reference

April 2022 Public Data File from Crossref

exact match

https://scigraph.springernature.com/pub.10.1186/1471-2105-12-68

0 references

cites work

A map of human genome variation from population-scale sequencing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3063825

Simultaneous genotype calling and haplotype phasing improves genotype accuracy and reduces false-positive associations for genome-wide association studies

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3063825

Quantifying uncertainty in genotype calls

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3063825

R/Bioconductor software for Illumina's Infinium whole-genome genotyping BeadChips.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3063825

Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3063825

Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3063825

Validation and extension of an empirical Bayes method for SNP calling on Affymetrix microarrays

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3063825

A second generation human haplotype map of over 3.1 million SNPs

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3063825

A genotype calling algorithm for the Illumina BeadArray platform

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3063825

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3063825

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3063825

Bioconductor: open software development for computational biology and bioinformatics

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3063825

A navigator for human genome epidemiology.

5 July 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2105-12-68

Whole-genome genotyping with the single-base extension assay

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2105-12-68

GenoSNP: a variational Bayes within-sample SNP genotyping algorithm that does not require a reference population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2105-12-68

Saliva-Derived DNA Performs Well in Large-Scale, High-Density Single-Nucleotide Polymorphism Microarray Studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2105-12-68

21 January 2018

Identifiers

DOI

10.1186/1471-2105-12-68

1 reference

journals/bmcbi/RitchieLCI11

29 July 2017

1 reference

DBLP Dataset 2021-01-02

Dimensions Publication ID

28 January 2021

0 references

1 reference

29 July 2017

1 reference

PubMed ID

21385424