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dnbseq g400 sequencer  (Complete Genomics Inc)


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    Complete Genomics Inc dnbseq g400 sequencer
    Dnbseq G400 Sequencer, supplied by Complete Genomics Inc, used in various techniques. Bioz Stars score: 99/100, based on 1633 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/dnbseq g400 sequencer/product/Complete Genomics Inc
    Average 99 stars, based on 1633 article reviews
    dnbseq g400 sequencer - by Bioz Stars, 2026-06
    99/100 stars

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    Pedigree and mutation analysis of the family. (A) Pedigrees of the GS families. The square represents male, and the circle represents female. The arrow represents the proband. The shaded symbol represents a homozygous (HOM) patient, the unshaded symbol represents wild-type (WT) individuals, and the half-shaded symbol represents a heterozygous patient. Draw a diagonal line through the square or circle represents the member is deceased. Age (B) and Body Mass Index (BMI) (C) of GS homozygous patients ( n = 5) and wild type individuals ( n = 7), ** p < 0.01. (D) Sanger sequencing validation of the SLC12A3 mutation (c.1262G > T) in the GS patients.

    Journal: Renal Failure

    Article Title: Serum metabolic profiling analysis of Gitelman syndrome using untargeted metabolomics

    doi: 10.1080/0886022X.2026.2662094

    Figure Lengend Snippet: Pedigree and mutation analysis of the family. (A) Pedigrees of the GS families. The square represents male, and the circle represents female. The arrow represents the proband. The shaded symbol represents a homozygous (HOM) patient, the unshaded symbol represents wild-type (WT) individuals, and the half-shaded symbol represents a heterozygous patient. Draw a diagonal line through the square or circle represents the member is deceased. Age (B) and Body Mass Index (BMI) (C) of GS homozygous patients ( n = 5) and wild type individuals ( n = 7), ** p < 0.01. (D) Sanger sequencing validation of the SLC12A3 mutation (c.1262G > T) in the GS patients.

    Article Snippet: Whole-exome sequencing (WES) was performed on all patients using the MGISEQ-2000 platform (MGI Tech) and validated by Sanger sequencing.

    Techniques: Mutagenesis, Sequencing, Biomarker Discovery