analysis software bioarray software environment database (Bioarray Inc)
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Bioarray Inc
analysis software bioarray software environment database
Analysis Software Bioarray Software Environment Database, supplied by Bioarray Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/software+environment+database/bioarray+software/us11261492-821-8-13
Average 90 stars, based on 1 article reviews
Analysis Software Bioarray Software Environment Database, supplied by Bioarray Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/software+environment+database/bioarray+software/us11261492-821-8-13
Average 90 stars, based on 1 article reviews
analysis software bioarray software environment database - by Bioz Stars,
2026-09
90/100 stars
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other:Article Title: Array-based genotype-phenotype correlation in a case of supernumerary ring chromosome 12. Article Snippet: Supernumerary ring chromosomes (SRC) account for approximately 10% of prenatal marker chromosomes and 60% of these SRCs are associated with an abnormal phenotype of the patient carrying them.. SRCs have, with few exceptions, not been characterized at the molecular genetic level.. Here, we present the first case of a SRC 12 thoroughly investigated with tiling resolution array-based comparative genomic hybridization (array CGH); multicolor, centromere, subtelomeric and whole chromosome painting fluorescence in situ hybridization. Article Title: Array based characterization of a terminal deletion involving chromosome subband 15q26.2: an emerging syndrome associated with growth retardation, cardiac defects and developmental delay Article Snippet: All normalizations and analyses were performed in the Article Title: dup(19)(q12q13.2): array-based genotype-phenotype correlation of a new possibly obesity-related syndrome. Article Snippet: All normalizations and analyses were performed in the Article Title: Toxicological and gene expression analysis of the impact of aflatoxin B1 on hepatic function of male broiler chicks. Article Snippet: The resulting files and images were linked together and stored in the local Article Title: Deletion of the SCN gene cluster on 2q24.4 is associated with severe epilepsy: an array-based genotype-phenotype correlation and a comprehensive review of previously published cases. Article Snippet: Epilepsy Research (2008) 81, 69—79 journa l homepage: www.e lsev ier .com/ locate /ep i lepsyres Deletion of the SCN gene cluster on 2q24.4 is associated with severe epilepsy: An array-based genotype—phenotype correlation and a comprehensive review of previously published cases Josef Davidssona,∗, Anna Collina, Mia Engman Olssonb, Johan Lundgrenc, Maria Sollera a Department of Clinical Genetics, Lund University Hospital, SE-221 85 Lund, Sweden b Department of Pediatrics, Karlskrona Hospital, Karlskrona, Sweden c Department of Pediatrics, Lund University Hospital, Lund, Sweden Received 17 December 2007; received in revised form 13 March 2008; accepted 22 April 2008 Available online 9 June 2008 KEYWORDS Severe epilepsy; SCN1A; del(2)(q24); Array CGH Summary Purpose: To characterize a deletion of chromosome 2q at the molecular level in a patient suffering from severe epilepsy resembling severe myoclonic epilepsy of infancy/Dravet’s syndrome (SMEI/DS) and to correlate other cases harboring deletions in the same region to morphological and clinical data.. Methods: Array-based comparative genomic hybridization (array CGH) was performed on DNA from the patient.. Forty-three previously published cases reporting deletions within region 2q21q31 were collected and analyzed regarding their cytogenetic and clinical data. Article Title: Sublethal effects of waterborne uranium exposures on the zebrafish brain: transcriptional responses and alterations of the olfactory bulb ultrastructure. Article Snippet: A D É L A Ï D E L E R E B O U R S , † J E A N P A U L B O U R D I N E A U D , ‡ K A R L I J N V A N D E R V E N , § T I N E V A N D E N B R O U C K , § P A T R I C E G O N Z A L E Z , ‡ V I R G I N I E C A M I L L E R I , † M A G A L I F L O R I A N I , † J A C Q U E L I N E G A R N I E R L A P L A C E , † A N D C H R I S T E L L E A D A M G U I L L E R M I N * , † Laboratoire de Radioécologie et d’Ecotoxicologie, Institut de Radioprotection et de Sûreté Nucléaire, Bât 186, BP 3, 13115 Saint-Paul-Lez-Durance Cedex, France Equipe de Géochimie et Ecotoxicologie des Métaux dans les systèmes Aquatiques (GEMA), UMR 5805 CNRSsUniversité Bordeaux 1, Place du Dr Peyneau, 33120 Arcachon, France Department of Biology, Laboratory of Ecophysiology, Biochemistry and Toxicology, University of Antwerp, Groeneborgerlaan 171, 2020 Antwerp, Belgium Article Title: Identification of molecules derived from human fibroblast feeder cells that support the proliferation of human embryonic stem cells Article Snippet: All of the normalizations, filtering, merging of technical replicates and analyses were performed in the Filtration:Article Title: Tiling resolution array CGH of dic(7;9)(p11 approximately 13;p11 approximately 13) in B-cell precursor acute lymphoblastic leukemia reveals clustered breakpoints at 7p11.2 approximately 12.1 and 9p13.1. Article Snippet: a Department of Clinical Genetics and b Department of Oncology, Lund University Hospital, Lund c Lund Strategic Research Center for Stem Cell Biology and Cell Therapy, Lund University, Lund (Sweden) d Department of Medical Genetics and Molecular Medicine, Haukeland University Hospital, Helse-Bergen HF e Department of Medical Genetics, Rikshospitalet-Radiumhospitalet Medical Centre, Oslo f University of Oslo, Oslo (Norway) |
