nextgene v2.4.1.2 software (SoftGenetics)
90
Structured Review
SoftGenetics
nextgene v2.4.1.2 software
Nextgene V2.4.1.2 Software, supplied by SoftGenetics, 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/nextgene+v2%2E4%2E1%2E2+software/nextgene+software/pm40102912-71-17-20
Average 90 stars, based on 1 article reviews
Nextgene V2.4.1.2 Software, supplied by SoftGenetics, 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/nextgene+v2%2E4%2E1%2E2+software/nextgene+software/pm40102912-71-17-20
Average 90 stars, based on 1 article reviews
nextgene v2.4.1.2 software - by Bioz Stars,
2026-09
90/100 stars
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Related Articles
Sequencing:Article Title: Exome sequencing improves genetic diagnosis of fetal increased nuchal translucency. Article Snippet: OBJECTIVE The aim of this retrospective study is to determine the monogenic syndromes in fetuses with isolated first-trimester increased nuchal translucency (NT) in order to provide more accurate parental counseling.. METHOD Medical trio exome sequencing (ES) was performed on DNA extracted from chorionic villi in 73 fetuses with isolated first-trimester increased NT (≥3.5mm) and normal chromosomal microarray analysis (CMA).. This testing targets coding exons for 4200 clinically relevant disease-causing genes. Article Title: Novel POMT2 variants associated with limb-girdle muscular dystrophy R14: genetic, histological and functional studies Article Snippet: Sequencing reads were aligned to the human reference genome (GRCh37/hg19), and variant calling was performed using Article Title: Genetic burden in neonatal and pediatric-onset pulmonary hypertension: A single-center retrospective study using exome sequencing in a Chinese population. Article Snippet: Article Title: Clinical exome sequencing identifies novel compound heterozygous mutations of the POMT2 gene in patients with limb-girdle muscular dystrophy. Article Snippet: Department of Clinical Laboratory, Linyi People’s Hospital, Shandong University, Linyi, China Department of Central Laboratory, Linyi People’s Hospital, Shandong University, Linyi, China Department of Neurology, Linyi People’s Hospital, Shandong University, Linyi, China Key Laboratory for Experimental Teratology of the Ministry of Education, Department of Medical Genetics, School of Basic Medical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, China Article Title: Prenatal Diagnosis and Outcomes in Fetuses with Hemivertebra Article Snippet: Article Title: Novel POMT2 variants associated with limb-girdle muscular dystrophy R14: genetic, histological and functional studies. Article Snippet: Sequencing reads were aligned to the human reference genome (GRCh37/ hg19), and variant calling was performed using Variant Assay:Article Title: Exome sequencing improves genetic diagnosis of fetal increased nuchal translucency. Article Snippet: OBJECTIVE The aim of this retrospective study is to determine the monogenic syndromes in fetuses with isolated first-trimester increased nuchal translucency (NT) in order to provide more accurate parental counseling.. METHOD Medical trio exome sequencing (ES) was performed on DNA extracted from chorionic villi in 73 fetuses with isolated first-trimester increased NT (≥3.5mm) and normal chromosomal microarray analysis (CMA).. This testing targets coding exons for 4200 clinically relevant disease-causing genes. Article Title: Novel POMT2 variants associated with limb-girdle muscular dystrophy R14: genetic, histological and functional studies Article Snippet: Sequencing reads were aligned to the human reference genome (GRCh37/hg19), and variant calling was performed using Article Title: Genetic burden in neonatal and pediatric-onset pulmonary hypertension: A single-center retrospective study using exome sequencing in a Chinese population. Article Snippet: Article Title: Clinical exome sequencing identifies novel compound heterozygous mutations of the POMT2 gene in patients with limb-girdle muscular dystrophy. Article Snippet: Department of Clinical Laboratory, Linyi People’s Hospital, Shandong University, Linyi, China Department of Central Laboratory, Linyi People’s Hospital, Shandong University, Linyi, China Department of Neurology, Linyi People’s Hospital, Shandong University, Linyi, China Key Laboratory for Experimental Teratology of the Ministry of Education, Department of Medical Genetics, School of Basic Medical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, China Article Title: Prenatal Diagnosis and Outcomes in Fetuses with Hemivertebra Article Snippet: Article Title: Novel POMT2 variants associated with limb-girdle muscular dystrophy R14: genetic, histological and functional studies. Article Snippet: Sequencing reads were aligned to the human reference genome (GRCh37/ hg19), and variant calling was performed using Software:Article Title: Exome sequencing improves genetic diagnosis of fetal increased nuchal translucency. Article Snippet: OBJECTIVE The aim of this retrospective study is to determine the monogenic syndromes in fetuses with isolated first-trimester increased nuchal translucency (NT) in order to provide more accurate parental counseling.. METHOD Medical trio exome sequencing (ES) was performed on DNA extracted from chorionic villi in 73 fetuses with isolated first-trimester increased NT (≥3.5mm) and normal chromosomal microarray analysis (CMA).. This testing targets coding exons for 4200 clinically relevant disease-causing genes. Article Title: Novel POMT2 variants associated with limb-girdle muscular dystrophy R14: genetic, histological and functional studies Article Snippet: Sequencing reads were aligned to the human reference genome (GRCh37/hg19), and variant calling was performed using Article Title: Genetic burden in neonatal and pediatric-onset pulmonary hypertension: A single-center retrospective study using exome sequencing in a Chinese population. Article Snippet: Article Title: Clinical exome sequencing identifies novel compound heterozygous mutations of the POMT2 gene in patients with limb-girdle muscular dystrophy. Article Snippet: Department of Clinical Laboratory, Linyi People’s Hospital, Shandong University, Linyi, China Department of Central Laboratory, Linyi People’s Hospital, Shandong University, Linyi, China Department of Neurology, Linyi People’s Hospital, Shandong University, Linyi, China Key Laboratory for Experimental Teratology of the Ministry of Education, Department of Medical Genetics, School of Basic Medical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, China Article Title: Prenatal Diagnosis and Outcomes in Fetuses with Hemivertebra Article Snippet: Article Title: Novel POMT2 variants associated with limb-girdle muscular dystrophy R14: genetic, histological and functional studies. Article Snippet: Sequencing reads were aligned to the human reference genome (GRCh37/ hg19), and variant calling was performed using |