Agilent Technologies’ Custom-Designed CGH Microarray Used to Map Korean Genome
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Agilent Technologies Inc. has announced that scientists using an Agilent custom-designed comparative genomic hybridization (CGH) array have sequenced the entire gene map of a Korean male. An international team led by researchers at Seoul National University published the results in Nature.
The study, “A highly annotated whole-genome sequence of a Korean individual,” published July 8 in Nature, is the second Korean genome to be sequenced in recent months and the seventh complete human genome to be published in the past two years.
“Through our studies, we have discovered that a much more accurate annotation of CNVs [copy number variants] can be obtained for a given individual’s genome when you combine data from high-resolution CGH experiments with whole-genome DNA sequencing data obtained using next-generation sequencing strategies,” said Dr. Charles Lee, associate professor, Harvard Medical School and Brigham & Women’s Hospital, and one of the researchers of study.
“In this case, we developed and used a customized, high-resolution CNV array set, manufactured by Agilent, containing 24 million oligonucleotide probes. It would be great to see similar approaches being used for comprehensively identifying CNVs in more individuals.”
The Seoul National University team used several complementary approaches to detect CNVs, including an Agilent custom-designed CGH array with more than 24 million probes.
The team initially identified 1,237 CNV regions, but used conservative criteria to cut that down to 238 deletions ranging from 277 bases to 196,900 bases and totaling 2.4 megabases, and 77 copy number gains, totaling 7 megabases. Of these CNVs, 148 of the deletions and 33 of the gains were not in the Database of Genomic Variants and are considered to be novel.
“This breakthrough study is a prime example of how Agilent’s custom microarray platform, which includes a comprehensive probe database, can advance structural variation research,” said Chris Grimley, Agilent senior marketing director, Genomics. “Agilent’s CGH/CNV microarrays offer the highest sensitivity and specificity of any platform.”
Agilent’s custom microarrays offer the flexibility needed to detect CNVs. The platform offers high-quality long oligonucleotide catalogue and custom arrays to interrogate any genome at high-resolution. Agilent’s custom arrays allow users to select the regions of the genome (or the entire genome) they want to target.
With 28.7 million in-silico-validated probes available in eArray, Agilent’s online tool for design custom arrays, researchers can choose what regions, resolution and array format they want for a given study. Custom arrays are available in all eight formats from Agilent at no additional cost to the user.
The study, “A highly annotated whole-genome sequence of a Korean individual,” published July 8 in Nature, is the second Korean genome to be sequenced in recent months and the seventh complete human genome to be published in the past two years.
“Through our studies, we have discovered that a much more accurate annotation of CNVs [copy number variants] can be obtained for a given individual’s genome when you combine data from high-resolution CGH experiments with whole-genome DNA sequencing data obtained using next-generation sequencing strategies,” said Dr. Charles Lee, associate professor, Harvard Medical School and Brigham & Women’s Hospital, and one of the researchers of study.
“In this case, we developed and used a customized, high-resolution CNV array set, manufactured by Agilent, containing 24 million oligonucleotide probes. It would be great to see similar approaches being used for comprehensively identifying CNVs in more individuals.”
The Seoul National University team used several complementary approaches to detect CNVs, including an Agilent custom-designed CGH array with more than 24 million probes.
The team initially identified 1,237 CNV regions, but used conservative criteria to cut that down to 238 deletions ranging from 277 bases to 196,900 bases and totaling 2.4 megabases, and 77 copy number gains, totaling 7 megabases. Of these CNVs, 148 of the deletions and 33 of the gains were not in the Database of Genomic Variants and are considered to be novel.
“This breakthrough study is a prime example of how Agilent’s custom microarray platform, which includes a comprehensive probe database, can advance structural variation research,” said Chris Grimley, Agilent senior marketing director, Genomics. “Agilent’s CGH/CNV microarrays offer the highest sensitivity and specificity of any platform.”
Agilent’s custom microarrays offer the flexibility needed to detect CNVs. The platform offers high-quality long oligonucleotide catalogue and custom arrays to interrogate any genome at high-resolution. Agilent’s custom arrays allow users to select the regions of the genome (or the entire genome) they want to target.
With 28.7 million in-silico-validated probes available in eArray, Agilent’s online tool for design custom arrays, researchers can choose what regions, resolution and array format they want for a given study. Custom arrays are available in all eight formats from Agilent at no additional cost to the user.
