
GenetiSure Postnatal Research Array (2x400K)
Updated CGH probe content targeted to regions of the genome known to be disease-associated can be easily sourced from the ClinGen/ISCA database.
- Human Microarrays
Product Details
- Maximize the detection of aberrations associated with intellectual disability and congenital anomalies with exon-centric probes.
- Single exon copy number detection for a clearer workflow.
- Covers disease-associated regions recommended by ClinGen/ISCA databases.
- 89% of the exon is covered with three or more probes during analysis.
- The median CGH probe spacing is approximately 9.8 KB overall.
- The system contains ~300,000 CGH probes and ~103,000 SNP probes.
- The probe standard 2x400 format can also be customized for other sizes and genes may be added or removed to further customize the array.
- Benefit from a complete workflow provided by a single supplier.
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Array Dimension |
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Array Type |
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Arrays per Slide |
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Composition Genome |
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Exon Coverage |
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LOH Resolution |
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Manufacturing Process |
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Minimum Probes per Exon |
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Number of Probes |
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Overall Median Probe Spacing |
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Replicates of Biological Probes |
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Samples per Kit |
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Slides per Kit |
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- Application Notes
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Agilent CGH+SNP Microarrays Demonstrate Superior Copy Number Calling for Cytogenetic Profiling of Hematological Cancer Samples
In this application note, we compare the quality of copy number and LOH data obtained with Agilent
- Application Notes
- English
- 08 Apr 2016
- 466.72 KB
- Brochures
- Catalogs
- Technical Overviews
- User Manuals
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Oligonucleotide aCGH for gDNA Analysis - Enzymatic Labeling For Blood, Cells, or Tissues (with a High Throughput option)
Oligonucleotide Array-Based CGH for Genomic DNA Analysis - Enzymatic Labeling For Blood, Cells, or Tissues (with a High Throughput option) Protocol
- User Manuals
- English
- 04 Mar 2020
- 4.63 MB
Oligonucleotide Array-Based CGH for Single Cell Analysis - Enzymatic Labeling Protocol A1
Oligonucleotide Array-Based CGH for Single Cell Analysis - Enzymatic Labeling Protocol A1
- User Manuals
- English
- 25 Aug 2015
- 2.43 MB
Oligonucleotide aCGH for Genomic DNA Analysis - ULS Labeling v.3.5
CGH ULS Protocol 3.5
- User Manuals
- English
- 25 Aug 2015
- 2.73 MB
Oligonucleotide Array-Based CGH for Genomics DNA Analysis- Bravo Automated Liquid Handling Platform with Enzymatic and ULS Labeling Protocol 2.3
Oligonucleotide Array-Based CGH for Genomics DNA Analysis- Bravo Automated Liquid Handling Platform with Enzymatic and ULS Labeling Protocol 2.3
- User Manuals
- English
- 25 Aug 2015
- 3.09 MB
- Publications
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- Pinto D et al. Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants. Nat Biotechnol. 2011 May 8;29(6):512-20. doi: 10.1038/nbt.1852 [Application: General] Learn More
- Alesi V et al. Easychip 8x15k: A New Tool for Detecting Chromosome Anomalies in Low Risk Pregnancies, Supporting and Integrating Standard Karyotype J Genet Syndr Gene Ther 7: 277. doi:10.4172/2157-7412.1000277 [Application: Prenatal] Learn More
- Chau MHK et al. Characteristics and mode of inheritance of pathogenic copy number variants in prenatal diagnosis. Am J Obstet Gynecol. 2019 Nov;221(5):493.e1-493.e11. doi: 10.1016/j.ajog.2019.06.007. Epub 2019 Jun 14. [Application: Prenatal] Learn More
- Ribeiro et al. Upper aerodigestive tract carcinoma: Development of a (epi)genomic predictive model for recurrence and metastasis. Oncol Lett. 2020 May;19(5):3459-3468. doi: 10.3892/ol.2020.11459. Epub 2020 Mar 12 [Application: Cancer] Learn More
- Kaur et al. Clinical impact of chromothriptic complex chromosomal rearrangements in newly diagnosed multiple myeloma. Leuk Res. 2019 Jan;76:58-64. doi: 10.1016/j.leukres.2018.12.005 [Application: Cancer] Learn More
Microrray Quality Information
Lot quality data and product identification information for microarrays manufactured after May 22, 2013.
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Surescan Reagent Rental
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