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MyGenostics Inc biotinylated capture probes
Biotinylated Capture Probes, supplied by MyGenostics 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/biotinylated+capture+probe/biotinylated+capture+probe/pm40075430-44-4-18
Average 90 stars, based on 1 article reviews
biotinylated capture probes - by Bioz Stars, 2026-09
90/100 stars

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Article Title: Phenotypic and genotypic correlation evaluation of 148 pediatric patients with Fanconi anemia in a Chinese rare disease cohort.
Article Snippet: Background: Fanconi anemia (FA) is a rare autosomal recessive, X-linked or autosomal dominant disease.. Few large-scale FA investigations of rare disease cohorts have been conducted in China.. Methods: We enrolled 148 patients diagnosed with FA according to evidence from the clinical phenotype, family history, and a set of laboratory tests.

Article Title: Novel diagnostic approaches for Fanconi anemia (FA) by single-cell sequencing and capillary nano-immunoassay
Article Snippet: A total of 417 blood disease genes were enriched through a biotinylated capture probe (MyGenostics, Baltimore, MD, USA), as described previously.

Article Title: Gene mutations in sporadic lymphangioleiomyomatosis and genotype-phenotype correlation analysis.
Article Snippet: Briefly, targeted genes were enriched using a biotinylated capture probe (MyGenostics, Baltimore, MD, USA) [21] and sequenced using the Illumina NextSeq500 platform (Illumina, San Diego, CA, USA).

Article Title: Gene mutations in sporadic lymphangioleiomyomatosis and genotype–phenotype correlation analysis
Article Snippet: Briefly, targeted genes were enriched using a biotinylated capture probe (MyGenostics, Baltimore, MD, USA) [ ] and sequenced using the Illumina NextSeq500 platform (Illumina, San Diego, CA, USA).

Article Title: Severe high-molecular-weight kininogen deficiency due to a homozygous c.1456C > T nonsense variant in a large Chinese family.
Article Snippet: High-molecular-weight kininogen (HMWK) deficiency is a very rare hereditary disorder caused by a defect of Kininogen-1 gene (KGN1).. A 67-year-old asymptomatic male with an isolated prolonged activated partial thromboplastin time (aPTT) was recognized to have HMWK deficiency.. The propositus had less than 1% HMWK procoagulant activity.

Article Title: A novel recessive mutation affecting DNAJB6a causes myofibrillar myopathy
Article Snippet: The exon regions were specifically enriched using a biotinylated capture probe (MyGenostics, China).

Sequencing:

Article Title: Novel diagnostic approaches for Fanconi anemia (FA) by single-cell sequencing and capillary nano-immunoassay.
Article Snippet: .. A total of 417 blood disease genes were enriched through a biotinylated capture probe (MyGenostics, Baltimore, MD, USA), as described previously.24 Sanger sequencing was then performed to analyze the potential gene mutations. ..



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