sureselect v5 exome capture kit (Agilent technologies)
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sureselect v5 exome capture kit
Sureselect V5 Exome Capture Kit, supplied by Agilent technologies, 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/sureselect+v5+kit/nct05722990-24-9-14
Average 90 stars, based on 1 article reviews
Sureselect V5 Exome Capture Kit, supplied by Agilent technologies, 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/sureselect+v5+kit/nct05722990-24-9-14
Average 90 stars, based on 1 article reviews
sureselect v5 exome capture kit - by Bioz Stars,
2026-09
90/100 stars
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Construct:Article Title: Exome analysis for Cronkhite-Canada syndrome: A case report Article Snippet: Next, PE150 high-throughput sequencing was performed based on the Illumina Hiseq platform. .. Finally, the library and capture experiment were constructed using the Control:Article Title: Novel heterozygous sequence variant in the GLI1 underlies postaxial polydactyly. Article Snippet: Polydactyly is one of the most common congenital abnormal phenotype of autopod, which is characterized by extra supernumerary digit in hands/feet with or without well-developed bony structure within the digits.. Preaxial polydactyly (PPD), postaxial polydactyly (PAP), and mesoaxial (central) polydactyly are three different isoforms of polydactyly.. Genetically, at least ten genes have been identified causing non-syndromic polydactyly. Sequencing:Article Title: BTB domain mutations perturbing KCTD15 oligomerisation cause a distinctive frontonasal dysplasia syndrome. Article Snippet: .. For Family 1 we used a previously described protocol22 to capture human genomic DNA using the Article Title: JAK2 regulates paclitaxel resistance in triple negative breast cancers. Article Snippet: We investigated the molecular mechanisms of paclitaxel resistance in TNBC using seven patient-derived xenograft (PDX) models and TNBC cell lines.. Among the seven PDX models, four models showed resistance to paclitaxel.. Dysregulation of JAK/STAT pathways and JAK2 copy number gains were observed in the four paclitaxel-resistant PDX tumors. Article Title: BTB domain mutations perturbing KCTD15 oligomerisation cause a distinctive frontonasal dysplasia syndrome Article Snippet: .. For Family 1 we used a previously described protocol to capture human genomic DNA using the Article Title: Pyrroline-5-carboxylate reductase 2 (PYCR2) deficiency causes hereditary spastic paraplaegia in late childhood. Article Snippet: Objectives: PYCR2 gene variants are extremely rare condition which is associated with hypomyelinating leukodystrophy type 10 with microcephaly (HLD10).. The aim of the present study is to report the clinical findings of patients having novel PYCR2 gene variant that manifest Hereditary Spastic Paraplegia (HSP) is the only symptom without hypomyelinating leukodystrophy.. This is the first study that report the PYCR2 gene variants as a cause of HSP in late childhood. RNA Sequencing:Article Title: JAK2 regulates paclitaxel resistance in triple negative breast cancers. Article Snippet: We investigated the molecular mechanisms of paclitaxel resistance in TNBC using seven patient-derived xenograft (PDX) models and TNBC cell lines.. Among the seven PDX models, four models showed resistance to paclitaxel.. Dysregulation of JAK/STAT pathways and JAK2 copy number gains were observed in the four paclitaxel-resistant PDX tumors. |