Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platforms (Q36959677)

17 August 2017

Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platforms (English)

1 reference

17 August 2017

1 reference

whole genome sequencing

1 reference

6

Hakon Hakonarson

1 reference

17 August 2017

9

Kai Wang

1 reference

17 August 2017

1

Sharon J Diskin

1 reference

17 August 2017

8

John M Maris

1 reference

17 August 2017

3

Cuiping Hou

1 reference

17 August 2017

7

Maja Bucan

1 reference

17 August 2017

5

Joseph Glessner

1 reference

17 August 2017

Mingyao Li

2

1 reference

17 August 2017

Shuzhang Yang

series ordinal

4

1 reference

17 August 2017

language of work or name

English

0 references

publication date

10 September 2008

1 reference

17 August 2017

Nucleic Acids Research

1 reference

17 August 2017

36

1 reference

17 August 2017

19

1 reference

17 August 2017

e126

1 reference

Chromosome 6p22 locus associated with clinically aggressive neuroblastoma

17 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2577347

The UCSC Genome Browser Database: 2008 update

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2577347

28-way vertebrate alignment and conservation track in the UCSC Genome Browser

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2577347

Breaking the waves: improved detection of copy number variation from microarray-based comparative genomic hybridization.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2577347

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2577347

Challenges and standards in integrating surveys of structural variation

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2577347

Methods and strategies for analyzing copy number variation using DNA microarrays

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2577347

The UCSC genome browser database: update 2007.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2577347

NCBI reference sequences (RefSeq): a curated non-redundant sequence database of genomes, transcripts and proteins

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2577347

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2577347

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2577347

Structural variation in the human genome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2577347

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2577347

Segmental duplications: organization and impact within the current human genome project assembly

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2577347

Tandem repeats finder: a program to analyze DNA sequences

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2577347

Whole-genome genotyping with the single-base extension assay

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2577347

4 September 2018

Identifiers

DOI

10.1093/NAR/GKN556

1 reference

17 August 2017

1 reference

17 August 2017

PubMed publication ID

18784189

1 reference