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Claritas Genomics
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BlueGnome Limited
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INFINIUM Inc
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23andMe
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INFINIUM Inc
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CombiMatrix
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Lineagen Inc
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Treff AG
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Thermo Fisher
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Treff AG
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Illumina Inc
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Image Search Results
Journal: PLoS ONE
Article Title: Identification of Chromosomal Errors in Human Preimplantation Embryos with Oligonucleotide DNA Microarray
doi: 10.1371/journal.pone.0061838
Figure Lengend Snippet: Microarray analysis of human blastocysts in patients undergoing in vitro fertilization and preimplantation genetic screening.
Article Snippet: One is a bacterial
Techniques: Microarray, In Vitro
Journal: PLoS ONE
Article Title: Identification of Chromosomal Errors in Human Preimplantation Embryos with Oligonucleotide DNA Microarray
doi: 10.1371/journal.pone.0061838
Figure Lengend Snippet: Detailed information of human blastocysts analyzed by oligo microarray in the patients without euploid blastocyst.
Article Snippet: One is a bacterial
Techniques: Microarray
Journal: PLoS ONE
Article Title: Identification of Chromosomal Errors in Human Preimplantation Embryos with Oligonucleotide DNA Microarray
doi: 10.1371/journal.pone.0061838
Figure Lengend Snippet: Detailed analysis of patients who had PGS by microarray and frozen embryo transfer.
Article Snippet: One is a bacterial
Techniques: Microarray
Journal: PLoS ONE
Article Title: Identification of Chromosomal Errors in Human Preimplantation Embryos with Oligonucleotide DNA Microarray
doi: 10.1371/journal.pone.0061838
Figure Lengend Snippet: Clinical outcome of patients who had PGS by microarray and embryo transfer.
Article Snippet: One is a bacterial
Techniques: Microarray
Journal: Discovery medicine
Article Title: Implementation of Biomarker-Driven Cancer Therapy: Existing Tools and Remaining Gaps
doi:
Figure Lengend Snippet: Examples of Cancer Gene Panels.
Article Snippet: Human Genotyping Array , 23 chromosome pairs , Assays 1million reported
Techniques: Sequencing, Amplification, Diagnostic Assay, Microarray
Journal: Journal of Pediatric Genetics
Article Title: Case Report of Proliferative Peripheral Retinopathy in Two Familial Lissencephaly Infants with Miller–Dieker Syndrome
doi: 10.1055/s-0037-1612638
Figure Lengend Snippet: Case #2's CGH analysis (DNAarrayTM-Oligi-180) revealed ( A ) a single copy number decrease of 3.0 Mb of chromosome 17p13.3 region and ( B ) a single copy increase of 2.0 Mb of chromosome 16p13.3 region consistent with a 17p13.3 microdeletion and a 16p13.3 microduplication. The derivative chromosome likely represents a malsegregation of a paternal balanced chromosome 16;17 translocation. The 16p duplication does not encompass the CREBBP gene within the Rubenstein–Taybi critical region. CGH, comparative genomic hybridization; CREBBP, CREB binding protein (CREB, cAMP response element binding protein binding protein).
Article Snippet:
Techniques: Translocation Assay, Hybridization, Binding Assay, Protein Binding