(Q38441304)

3 September 2017

Whole genome SNP arrays using DNA derived from formalin-fixed, paraffin-embedded ovarian tumor tissue (English)

1 reference

3 September 2017

whole genome sequencing

1 reference

4

Ian G Campbell

1 reference

3 September 2017

Ella R Thompson

1

1 reference

PubMed ID

16116623

3 September 2017

Shane C Herbert

series ordinal

2

1 reference

PubMed ID

16116623

3 September 2017

Susan M Forrest

series ordinal

3

1 reference

3 September 2017

1 October 2005

1 reference

3 September 2017

1 reference

3 September 2017

26

1 reference

3 September 2017

384-389

1 reference

3 September 2017

4

1 reference

Whole genome DNA copy number changes identified by high density oligonucleotide arrays

3 September 2017

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20220

High-resolution analysis of DNA copy number using oligonucleotide microarrays

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20220

7 January 2021

High-resolution single-nucleotide polymorphism array and clustering analysis of loss of heterozygosity in human lung cancer cell lines

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20220

7 January 2021

Large-scale genotyping of complex DNA.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20220

7 January 2021

Parallel genotyping of over 10,000 SNPs using a one-primer assay on a high-density oligonucleotide array

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20220

7 January 2021

Genomewide linkage analysis of bipolar disorder by use of a high-density single-nucleotide-polymorphism (SNP) genotyping assay: a comparison with microsatellite marker assays and finding of significant linkage to chromosome 6q22.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20220

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20220

7 January 2021

Concurrent analysis of loss of heterozygosity (LOH) and copy number abnormality (CNA) for oral premalignancy progression using the Affymetrix 10K SNP mapping array

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20220

7 January 2021

Identifiers

DOI

10.1002/HUMU.20220

1 reference

3 September 2017

1 reference

PubMed ID

16116623