Rapid detection of structural variation in a human genome using nanochannel-based genome mapping technology (Q35066595)

6 August 2017

Rapid detection of structural variation in a human genome using nanochannel-based genome mapping technology (English)

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6 August 2017

15

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6 August 2017

16

Huanming Yang

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6 August 2017

Hongzhi Cao

1

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6 August 2017

Alex R Hastie

2

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6 August 2017

Dandan Cao

3

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6 August 2017

Ernest T Lam

4

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6 August 2017

Yuhui Sun

5

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6 August 2017

Haodong Huang

6

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6 August 2017

Xiao Liu

7

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6 August 2017

Liya Lin

8

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6 August 2017

Warren Andrews

9

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6 August 2017

Saki Chan

10

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6 August 2017

Shujia Huang

11

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6 August 2017

Xin Tong

12

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6 August 2017

Michael Requa

13

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6 August 2017

Thomas Anantharaman

14

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6 August 2017

Han Cao

17

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6 August 2017

Xun Xu

18

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6 August 2017

30 December 2014

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3

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1

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6 August 2017

34

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https://scigraph.springernature.com/pub.10.1186/2047-217x-3-34

6 August 2017

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8 July 2018

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8 July 2018

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8 July 2018

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8 July 2018

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Phenotypic impact of genomic structural variation: insights from and for human disease

8 July 2018

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Genome mapping on nanochannel arrays for structural variation analysis and sequence assembly

8 July 2018

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8 July 2018

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CREST maps somatic structural variation in cancer genomes with base-pair resolution.

8 July 2018

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Genome structural variation discovery and genotyping

8 July 2018

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CNVnator: an approach to discover, genotype, and characterize typical and atypical CNVs from family and population genome sequencing

8 July 2018

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Mapping copy number variation by population-scale genome sequencing

8 July 2018

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Limitations of next-generation genome sequence assembly

8 July 2018

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A map of human genome variation from population-scale sequencing

8 July 2018

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Single molecule linear analysis of DNA in nano-channel labeled with sequence specific fluorescent probes

8 July 2018

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High-resolution human genome structure by single-molecule analysis

8 July 2018

1 reference

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Structural variation in the human genome and its role in disease

8 July 2018

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BreakDancer: an algorithm for high-resolution mapping of genomic structural variation

8 July 2018

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Population analysis of large copy number variants and hotspots of human genetic disease

8 July 2018

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The diploid genome sequence of an Asian individual

8 July 2018

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4322599

Mapping and sequencing of structural variation from eight human genomes

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4322599

Variation analysis and gene annotation of eight MHC haplotypes: the MHC Haplotype Project

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4322599

Immunoglobulin gene rearrangements and the pathogenesis of multiple myeloma.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4322599

Genomic rearrangements and sporadic disease

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4322599

Strong association of de novo copy number mutations with autism

8 July 2018

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Mendelian Inheritance in Man and its online version, OMIM

8 July 2018

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Gene discovery at the human T-cell receptor alpha/delta locus

8 July 2018

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Global variation in copy number in the human genome

8 July 2018

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An algorithm for assembly of ordered restriction maps from single DNA molecules

8 July 2018

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Copy number variation: new insights in genome diversity

8 July 2018

1 reference

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Structural variation in the human genome

8 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4322599

A genome-wide comparison of recent chimpanzee and human segmental duplications

8 July 2018

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Segmental duplications and copy-number variation in the human genome

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4322599

Fine-scale structural variation of the human genome

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4322599

Understanding how combinations of HLA and KIR genes influence disease

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4322599

Large-scale copy number polymorphism in the human genome

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4322599

Serum reference intervals and diagnostic ranges for free kappa and free lambda immunoglobulin light chains: relative sensitivity for detection of monoclonal light chains

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4322599

KIR: diverse, rapidly evolving receptors of innate and adaptive immunity

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4322599

A complete map of the human immunoglobulin VH locus

8 July 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4322599

8 July 2018

https://api.crossref.org/works/10.1186%2F2047-217X-3-34

Deletions of chromosome 15 as a cause of the Prader-Willi syndrome

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4322599

Analysis of immunoglobulin, T cell receptor and bcr rearrangements in human malignant lymphoma and Hodgkin's disease

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4322599

De novo assembly of a haplotype-resolved human genome.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4322599

Sequencing and automated whole-genome optical mapping of the genome of a domestic goat (Capra hircus).

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4322599

Human copy number variation and complex genetic disease.

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4322599

Structural variation in two human genomes mapped at single-nucleotide resolution by whole genome de novo assembly

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4322599

Visualization of episomal and integrated Epstein-Barr virus DNA by fiber fluorescence in situ hybridization

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4322599

Complete sequence and gene map of a human major histocompatibility complex. The MHC sequencing consortium

27 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186%2F2047-217X-3-34

21 January 2018

Identifiers

DOI

10.1186/2047-217X-3-34

1 reference

Dimensions Publication ID

6 August 2017

0 references

1 reference

6 August 2017

1 reference