(Q30501982)

13 October 2017

Inference of chromosome-specific copy numbers using population haplotypes (English)

1 reference

13 October 2017

Yao-Ting Huang

1

1 reference

PMC publication ID

3128032

13 October 2017

Min-Han Wu

series ordinal

2

1 reference

13 October 2017

24 May 2011

1 reference

13 October 2017

1 reference

13 October 2017

12

1 reference

13 October 2017

194

1 reference

Creative Commons Attribution 2.0 Generic

13 October 2017

start time

24 May 2011

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

1 reference

April 2022 Public Data File from Crossref

cites work

Founder population-specific HapMap panel increases power in GWA studies through improved imputation accuracy and CNV tagging

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128032

ACNE: a summarization method to estimate allele-specific copy numbers for Affymetrix SNP arrays

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128032

Inferring combined CNV/SNP haplotypes from genotype data

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128032

Origins and functional impact of copy number variation in the human genome

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128032

Personalized copy number and segmental duplication maps using next-generation sequencing.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128032

Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's disease

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128032

Next-generation DNA sequencing

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128032

Modeling genetic inheritance of copy number variations.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128032

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128032

An algorithm for inferring complex haplotypes in a region of copy-number variation

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128032

MOCSphaser: a haplotype inference tool from a mixture of copy number variation and single nucleotide polymorphism data

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128032

Mapping and sequencing of structural variation from eight human genomes

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128032

Genome-wide detection and characterization of positive selection in human populations

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128032

A second generation human haplotype map of over 3.1 million SNPs

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128032

Major changes in our DNA lead to major changes in our thinking

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128032

Global variation in copy number in the human genome

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128032

Cytogenetically balanced translocations are associated with focal copy number alterations

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128032

Hotspots for copy number variation in chimpanzees and humans

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128032

APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128032

Selecting additional tag SNPs for tolerating missing data in genotyping.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128032

Human subtelomeres are hot spots of interchromosomal recombination and segmental duplication

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128032

A note on exact tests of Hardy-Weinberg equilibrium

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128032

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128032

alpha-Synuclein locus triplication causes Parkinson's disease

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128032

A comparison of bayesian methods for haplotype reconstruction from population genotype data

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3128032

Natural selection shapes genome-wide patterns of copy-number polymorphism in Drosophila melanogaster.

20 June 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2105-12-194

Common deletion polymorphisms in the human genome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2105-12-194

Multi-objective tag SNPs selection using evolutionary algorithms

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2105-12-194

HapCUT: an efficient and accurate algorithm for the haplotype assembly problem

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2105-12-194

An approximation algorithm for haplotype inference by maximum parsimony.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2105-12-194

Array CGH analysis of copy number variation identifies 1284 new genes variant in healthy white males: implications for association studies of complex diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2105-12-194

21 January 2018

Identifiers

DOI

10.1186/1471-2105-12-194

1 reference

13 October 2017

journals/bmcbi/HuangW11

1 reference

DBLP Dataset 2021-01-02

Dimensions Publication ID

28 January 2021

0 references

1 reference

PMC publication ID

3128032

13 October 2017

PubMed publication ID

21605463

1 reference

PMC publication ID

3128032