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MyGenostics Inc next-generation sequencing analysis
Next Generation Sequencing Analysis, 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/generation+sequencing/next+generation+sequencing/pmc08104201-3-1-9
Average 90 stars, based on 1 article reviews
next-generation sequencing analysis - by Bioz Stars, 2026-10
90/100 stars

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Article Title: Clinical and molecular genetic characteristics of pediatric PFIC3 patients: three novel variants and prognosis for parental liver transplantation.
Article Snippet: All three children were diagnosed through Next-Generation Sequencing (NGS), with genetic testing and analysis services conducted by the Beijing MyGenostics Medical Testing Institute.

Article Title: HDR syndrome presented with nephrotic syndrome in a Chinese boy: A case report
Article Snippet: Genetic analysis was performed using next-generation sequencing at the genetics laboratories of the MyGenostics biotechnology company in China, using “the inherited renal diseases panel”, which covers genes strongly correlated with this disorder.

Article Title: Novel compound heterozygous mutations in LMAN2L cause early childhood refractory epilepsy.
Article Snippet: Clean reads were assembled and spliced using the secondgeneration sequencing analysis platform provided by MyGenostics and the coverage and sequencing quality of the target region were evaluated.

Article Title: Biliary, Renal, Neurological, and Skeletal syndrome in a Chinese boy.
Article Snippet: Genetic analysis was performed using next-generation sequencing in the genetics laboratories of MyGenostics biotechnology company in China, using a ciliopathy panel which covers 140 known genes strongly correlated with this disorder; the result revealed that the index * Hong-Wen Zhang zhanghongwen@126.com 1 Department of Pediatrics, Peking University First Hospital Ningxia Women and Children’s Hospital, Yinchuan 750001, China 2 Department of Pediatrics, Peking University First Hospital, Beijing 100034, China patient carried three novel compound heterozygous variants in the TTC26 gene, c.1069 + 5G > A (Variant of unknown significance, ACMG guideline: PM2_Supporting + PP3) in one allele from the mother, and c.511A > G (p.Ile171Val) (Variant of unknown significance, ACMG guideline: PM2_ Supporting) and c.1099T > C (p.Ser367Pro) (Variant of unknown significance, ACMG guideline: PM2_Supporting) in another allele from the father.

Sequencing:

Article Title: Investigating genetic variants in early-onset obesity through exome sequencing: A retrospective cohort study.
Article Snippet: Objective: This study aimed to examine clinical data and analyze exome sequencing (ES) findings in children diagnosed with early-onset obesity.. Methods: We screened children presenting with severe (body mass index-standard deviation score >3) and earlyonset (<7 years) obesity using ES.. Participants were categorized into either the "no variant identified" group or the "variant identified" group, facilitating the exploration of correlations between clinical-demographic characteristics and genetic mutations linked to early-onset obesity.

Article Title: Genetic and clinical profile of high myopia patients with rhegmatogenous retinal detachment
Article Snippet: .. Clean reads were then assembled and spliced using the MyGenostics second-generation sequencing analysis platform. ..

Article Title: Functional study of three cases with novel TBX19 variants.
Article Snippet: DNA was extracted from peripheral blood leukocytes using DNA extraction kit (Qiagen, Hilden, Germany). .. Probands were sequenced the initial next generation sequencing analysis (NGS: whole exome sequencing (WES)) and the identified variants were confirmed in the parents using Sanger sequencing (Mygenostics and Kindstar global, China). ..

Article Title: Novel compound heterozygous mutations in LMAN2L cause early childhood refractory epilepsy
Article Snippet: An Illumina Next Seq 500 sequencer (Illumina, San Diego, CA, USA) was used with 150 bp paired-end reads. .. Clean reads were assembled and spliced using the second-generation sequencing analysis platform provided by MyGenostics and the coverage and sequencing quality of the target region were evaluated. ..

Next-Generation Sequencing:

Article Title: Functional study of three cases with novel TBX19 variants.
Article Snippet: DNA was extracted from peripheral blood leukocytes using DNA extraction kit (Qiagen, Hilden, Germany). .. Probands were sequenced the initial next generation sequencing analysis (NGS: whole exome sequencing (WES)) and the identified variants were confirmed in the parents using Sanger sequencing (Mygenostics and Kindstar global, China). ..



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