(Q24613521)

2

0 references

Young Seok Ju

3

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Sheehyun Kim

4

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Jong-Yeon Shin

5

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Sujung Kim

6

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Saet-Byeol Yu

7

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Won-Chul Lee

8

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Seungbok Lee

9

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Hansoo Park

10

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Jong-Il Kim

11

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Jeong-Sun Seo

Creative Commons Attribution-NonCommercial 2.5 Generic

12

0 references

language of work or name

English

0 references

publication date

January 2011

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published in

Nucleic Acids Research

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volume

39

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issue

Database issue

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page(s)

D883-8

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copyright license

start time

14 November 2016

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

Personal genome sequencing: current approaches and challenges

1 reference

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Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding

7 April 2017

1 reference

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The diploid genome sequence of an Asian individual

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3013693

Accurate whole human genome sequencing using reversible terminator chemistry

7 April 2017

1 reference

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Paired-end mapping reveals extensive structural variation in the human genome

7 April 2017

1 reference

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The diploid genome sequence of an individual human

7 April 2017

1 reference

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Global variation in copy number in the human genome

7 April 2017

1 reference

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The complete genome of an individual by massively parallel DNA sequencing

7 April 2017

1 reference

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Detection of large-scale variation in the human genome

7 April 2017

1 reference

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Human genome sequencing using unchained base reads on self-assembling DNA nanoarrays

7 April 2017

1 reference

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Copy-number variation and association studies of human disease

7 April 2017

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Archiving next generation sequencing data

7 April 2017

1 reference

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

7 April 2017

1 reference

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The UCSC Genome Browser database: update 2010

7 April 2017

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Reference-unbiased copy number variant analysis using CGH microarrays

7 April 2017

1 reference

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Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing

27 September 2017

1 reference

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Fast and SNP-tolerant detection of complex variants and splicing in short reads

27 September 2017

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Ensembl Genomes: extending Ensembl across the taxonomic space

27 September 2017

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Single-molecule sequencing of an individual human genome

27 September 2017

1 reference

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A highly annotated whole-genome sequence of a Korean individual

27 September 2017

1 reference

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The YH database: the first Asian diploid genome database

27 September 2017

1 reference

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High-resolution mapping of copy-number alterations with massively parallel sequencing

27 September 2017

1 reference

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The fine-scale and complex architecture of human copy-number variation

27 September 2017

1 reference

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Efficient calculation of interval scores for DNA copy number data analysis

27 September 2017

1 reference

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Sensitive and accurate detection of copy number variants using read depth of coverage

27 September 2017

1 reference

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The HuRef Browser: a web resource for individual human genomics

30 May 2018

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journals/nar/HongPJKSKYLLPKS11

28 November 2018

Identifiers

DOI

10.1093/NAR/GKQ1101

0 references

DBLP publication ID

1 reference