rapid Search Results


ab 10 rapid fluorescein labeling kit  (Dojindo Labs)
92
Dojindo Labs ab 10 rapid fluorescein labeling kit
Ab 10 Rapid Fluorescein Labeling Kit, supplied by Dojindo Labs, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rapid/pm38797690-48-15-19?v=Dojindo+Labs
Average 92 stars, based on 1 article reviews
ab 10 rapid fluorescein labeling kit - by Bioz Stars, 2026-08
92/100 stars
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eco taq pcr super mix  (Vazyme Biotech Co)
97
Vazyme Biotech Co eco taq pcr super mix
Eco Taq Pcr Super Mix, supplied by Vazyme Biotech Co, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rapid/pmc12984350-107-30-35?v=Vazyme+Biotech+Co
Average 97 stars, based on 1 article reviews
eco taq pcr super mix - by Bioz Stars, 2026-08
97/100 stars
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trusight rapid  (Illumina Inc)
96
Illumina Inc trusight rapid
Figure 4 Pipeline analysis for targeted NGS of multiple inherited cancer syndromes using the <t>TruSight</t> Cancer panel. In our analysis pipeline, .fastq files are used for alignment and variant calling in Isaac Enrichment, Burrows-Wheeler Aligner (BWA) Enrichment, and NextGENe software, and .vcf files are then imported to GeneticistAssistant for variant filtering. Supervised analysis of filtered variants will allow the identification of disease-associated variants and/or of pathogenic variants associated with cancer predisposing syndromes outside the clinical context (incidental finding), with both being supported (if needed) by visual inspection of .bam files in Golden Helix GenomeBrowse (GB). Variants called because <t>of</t> <t>sequencing</t> errors are discarded on visual inspection of .bam files in Golden Helix GB. 1000G, 1000 Genomes Project; ACMG, American College of Med- ical Genetics and Genomics; Alt.var.freq., percentage of reads with alter- native allele; CDS, coding sequence; EVS, Exome Variant Server; ExAC, Exome Aggregation Consortium; In-house freq., variant frequency among all of the samples in our in-house database; MAF, minor allele frequency.
Trusight Rapid, supplied by Illumina Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rapid/pm28529006-32-12-16?v=Illumina+Inc
Average 96 stars, based on 1 article reviews
trusight rapid - by Bioz Stars, 2026-08
96/100 stars
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nucleospin dna rapidlyse kit  (MACHEREY NAGEL)
95
MACHEREY NAGEL nucleospin dna rapidlyse kit
Figure 4 Pipeline analysis for targeted NGS of multiple inherited cancer syndromes using the <t>TruSight</t> Cancer panel. In our analysis pipeline, .fastq files are used for alignment and variant calling in Isaac Enrichment, Burrows-Wheeler Aligner (BWA) Enrichment, and NextGENe software, and .vcf files are then imported to GeneticistAssistant for variant filtering. Supervised analysis of filtered variants will allow the identification of disease-associated variants and/or of pathogenic variants associated with cancer predisposing syndromes outside the clinical context (incidental finding), with both being supported (if needed) by visual inspection of .bam files in Golden Helix GenomeBrowse (GB). Variants called because <t>of</t> <t>sequencing</t> errors are discarded on visual inspection of .bam files in Golden Helix GB. 1000G, 1000 Genomes Project; ACMG, American College of Med- ical Genetics and Genomics; Alt.var.freq., percentage of reads with alter- native allele; CDS, coding sequence; EVS, Exome Variant Server; ExAC, Exome Aggregation Consortium; In-house freq., variant frequency among all of the samples in our in-house database; MAF, minor allele frequency.
Nucleospin Dna Rapidlyse Kit, supplied by MACHEREY NAGEL, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rapid/ppr0684057-75-13-17?v=MACHEREY+NAGEL
Average 95 stars, based on 1 article reviews
nucleospin dna rapidlyse kit - by Bioz Stars, 2026-08
95/100 stars
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tianprep rapid mini plasmid kit  (tiangen biotech co)
95
tiangen biotech co tianprep rapid mini plasmid kit
Figure 4 Pipeline analysis for targeted NGS of multiple inherited cancer syndromes using the <t>TruSight</t> Cancer panel. In our analysis pipeline, .fastq files are used for alignment and variant calling in Isaac Enrichment, Burrows-Wheeler Aligner (BWA) Enrichment, and NextGENe software, and .vcf files are then imported to GeneticistAssistant for variant filtering. Supervised analysis of filtered variants will allow the identification of disease-associated variants and/or of pathogenic variants associated with cancer predisposing syndromes outside the clinical context (incidental finding), with both being supported (if needed) by visual inspection of .bam files in Golden Helix GenomeBrowse (GB). Variants called because <t>of</t> <t>sequencing</t> errors are discarded on visual inspection of .bam files in Golden Helix GB. 1000G, 1000 Genomes Project; ACMG, American College of Med- ical Genetics and Genomics; Alt.var.freq., percentage of reads with alter- native allele; CDS, coding sequence; EVS, Exome Variant Server; ExAC, Exome Aggregation Consortium; In-house freq., variant frequency among all of the samples in our in-house database; MAF, minor allele frequency.
Tianprep Rapid Mini Plasmid Kit, supplied by tiangen biotech co, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rapid/pmc10686057-324-9-14?v=tiangen+biotech+co
Average 95 stars, based on 1 article reviews
tianprep rapid mini plasmid kit - by Bioz Stars, 2026-08
95/100 stars
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e z n a tianprep mini plasmid kit  (tiangen biotech co)
93
tiangen biotech co e z n a tianprep mini plasmid kit
Figure 4 Pipeline analysis for targeted NGS of multiple inherited cancer syndromes using the <t>TruSight</t> Cancer panel. In our analysis pipeline, .fastq files are used for alignment and variant calling in Isaac Enrichment, Burrows-Wheeler Aligner (BWA) Enrichment, and NextGENe software, and .vcf files are then imported to GeneticistAssistant for variant filtering. Supervised analysis of filtered variants will allow the identification of disease-associated variants and/or of pathogenic variants associated with cancer predisposing syndromes outside the clinical context (incidental finding), with both being supported (if needed) by visual inspection of .bam files in Golden Helix GenomeBrowse (GB). Variants called because <t>of</t> <t>sequencing</t> errors are discarded on visual inspection of .bam files in Golden Helix GB. 1000G, 1000 Genomes Project; ACMG, American College of Med- ical Genetics and Genomics; Alt.var.freq., percentage of reads with alter- native allele; CDS, coding sequence; EVS, Exome Variant Server; ExAC, Exome Aggregation Consortium; In-house freq., variant frequency among all of the samples in our in-house database; MAF, minor allele frequency.
E Z N A Tianprep Mini Plasmid Kit, supplied by tiangen biotech co, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rapid/pm40685341-38-0-7?v=tiangen+biotech+co
Average 93 stars, based on 1 article reviews
e z n a tianprep mini plasmid kit - by Bioz Stars, 2026-08
93/100 stars
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rapid capture enrichment kit  (Illumina Inc)
95
Illumina Inc rapid capture enrichment kit
Figure 4 Pipeline analysis for targeted NGS of multiple inherited cancer syndromes using the <t>TruSight</t> Cancer panel. In our analysis pipeline, .fastq files are used for alignment and variant calling in Isaac Enrichment, Burrows-Wheeler Aligner (BWA) Enrichment, and NextGENe software, and .vcf files are then imported to GeneticistAssistant for variant filtering. Supervised analysis of filtered variants will allow the identification of disease-associated variants and/or of pathogenic variants associated with cancer predisposing syndromes outside the clinical context (incidental finding), with both being supported (if needed) by visual inspection of .bam files in Golden Helix GenomeBrowse (GB). Variants called because <t>of</t> <t>sequencing</t> errors are discarded on visual inspection of .bam files in Golden Helix GB. 1000G, 1000 Genomes Project; ACMG, American College of Med- ical Genetics and Genomics; Alt.var.freq., percentage of reads with alter- native allele; CDS, coding sequence; EVS, Exome Variant Server; ExAC, Exome Aggregation Consortium; In-house freq., variant frequency among all of the samples in our in-house database; MAF, minor allele frequency.
Rapid Capture Enrichment Kit, supplied by Illumina Inc, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rapid/pmc06626132-230-6-10?v=Illumina+Inc
Average 95 stars, based on 1 article reviews
rapid capture enrichment kit - by Bioz Stars, 2026-08
95/100 stars
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lightning link rapid biotin antibody labeling kit  (Novus Biologicals)
94
Novus Biologicals lightning link rapid biotin antibody labeling kit
Figure 4 Pipeline analysis for targeted NGS of multiple inherited cancer syndromes using the <t>TruSight</t> Cancer panel. In our analysis pipeline, .fastq files are used for alignment and variant calling in Isaac Enrichment, Burrows-Wheeler Aligner (BWA) Enrichment, and NextGENe software, and .vcf files are then imported to GeneticistAssistant for variant filtering. Supervised analysis of filtered variants will allow the identification of disease-associated variants and/or of pathogenic variants associated with cancer predisposing syndromes outside the clinical context (incidental finding), with both being supported (if needed) by visual inspection of .bam files in Golden Helix GenomeBrowse (GB). Variants called because <t>of</t> <t>sequencing</t> errors are discarded on visual inspection of .bam files in Golden Helix GB. 1000G, 1000 Genomes Project; ACMG, American College of Med- ical Genetics and Genomics; Alt.var.freq., percentage of reads with alter- native allele; CDS, coding sequence; EVS, Exome Variant Server; ExAC, Exome Aggregation Consortium; In-house freq., variant frequency among all of the samples in our in-house database; MAF, minor allele frequency.
Lightning Link Rapid Biotin Antibody Labeling Kit, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rapid/pmc07312379-187-5-11?v=Novus+Biologicals
Average 94 stars, based on 1 article reviews
lightning link rapid biotin antibody labeling kit - by Bioz Stars, 2026-08
94/100 stars
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hiseq rapid pe cluster kit v2  (Illumina Inc)
95
Illumina Inc hiseq rapid pe cluster kit v2
Figure 4 Pipeline analysis for targeted NGS of multiple inherited cancer syndromes using the <t>TruSight</t> Cancer panel. In our analysis pipeline, .fastq files are used for alignment and variant calling in Isaac Enrichment, Burrows-Wheeler Aligner (BWA) Enrichment, and NextGENe software, and .vcf files are then imported to GeneticistAssistant for variant filtering. Supervised analysis of filtered variants will allow the identification of disease-associated variants and/or of pathogenic variants associated with cancer predisposing syndromes outside the clinical context (incidental finding), with both being supported (if needed) by visual inspection of .bam files in Golden Helix GenomeBrowse (GB). Variants called because <t>of</t> <t>sequencing</t> errors are discarded on visual inspection of .bam files in Golden Helix GB. 1000G, 1000 Genomes Project; ACMG, American College of Med- ical Genetics and Genomics; Alt.var.freq., percentage of reads with alter- native allele; CDS, coding sequence; EVS, Exome Variant Server; ExAC, Exome Aggregation Consortium; In-house freq., variant frequency among all of the samples in our in-house database; MAF, minor allele frequency.
Hiseq Rapid Pe Cluster Kit V2, supplied by Illumina Inc, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rapid/pmc07082340__41396_2019_571_MOESM1_ESM-23-18-47?v=Illumina+Inc
Average 95 stars, based on 1 article reviews
hiseq rapid pe cluster kit v2 - by Bioz Stars, 2026-08
95/100 stars
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incucyte zoom  (Sartorius AG)
99
Sartorius AG incucyte zoom
Figure 4 Pipeline analysis for targeted NGS of multiple inherited cancer syndromes using the <t>TruSight</t> Cancer panel. In our analysis pipeline, .fastq files are used for alignment and variant calling in Isaac Enrichment, Burrows-Wheeler Aligner (BWA) Enrichment, and NextGENe software, and .vcf files are then imported to GeneticistAssistant for variant filtering. Supervised analysis of filtered variants will allow the identification of disease-associated variants and/or of pathogenic variants associated with cancer predisposing syndromes outside the clinical context (incidental finding), with both being supported (if needed) by visual inspection of .bam files in Golden Helix GenomeBrowse (GB). Variants called because <t>of</t> <t>sequencing</t> errors are discarded on visual inspection of .bam files in Golden Helix GB. 1000G, 1000 Genomes Project; ACMG, American College of Med- ical Genetics and Genomics; Alt.var.freq., percentage of reads with alter- native allele; CDS, coding sequence; EVS, Exome Variant Server; ExAC, Exome Aggregation Consortium; In-house freq., variant frequency among all of the samples in our in-house database; MAF, minor allele frequency.
Incucyte Zoom, supplied by Sartorius AG, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rapid/pm41963733-271-9-11?v=Sartorius+AG
Average 99 stars, based on 1 article reviews
incucyte zoom - by Bioz Stars, 2026-08
99/100 stars
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e irr221 3 3 diaminobenzidine stain reagent dab super plustm high sensitive  (Elabscience Biotechnology)
96
Elabscience Biotechnology e irr221 3 3 diaminobenzidine stain reagent dab super plustm high sensitive
Figure 4 Pipeline analysis for targeted NGS of multiple inherited cancer syndromes using the <t>TruSight</t> Cancer panel. In our analysis pipeline, .fastq files are used for alignment and variant calling in Isaac Enrichment, Burrows-Wheeler Aligner (BWA) Enrichment, and NextGENe software, and .vcf files are then imported to GeneticistAssistant for variant filtering. Supervised analysis of filtered variants will allow the identification of disease-associated variants and/or of pathogenic variants associated with cancer predisposing syndromes outside the clinical context (incidental finding), with both being supported (if needed) by visual inspection of .bam files in Golden Helix GenomeBrowse (GB). Variants called because <t>of</t> <t>sequencing</t> errors are discarded on visual inspection of .bam files in Golden Helix GB. 1000G, 1000 Genomes Project; ACMG, American College of Med- ical Genetics and Genomics; Alt.var.freq., percentage of reads with alter- native allele; CDS, coding sequence; EVS, Exome Variant Server; ExAC, Exome Aggregation Consortium; In-house freq., variant frequency among all of the samples in our in-house database; MAF, minor allele frequency.
E Irr221 3 3 Diaminobenzidine Stain Reagent Dab Super Plustm High Sensitive, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rapid/10__26538_slash_tjnpr_slash_v8i3__22-79-8-5?v=Elabscience+Biotechnology
Average 96 stars, based on 1 article reviews
e irr221 3 3 diaminobenzidine stain reagent dab super plustm high sensitive - by Bioz Stars, 2026-08
96/100 stars
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library 186 concentration  (Illumina Inc)
95
Illumina Inc library 186 concentration
Figure 4 Pipeline analysis for targeted NGS of multiple inherited cancer syndromes using the <t>TruSight</t> Cancer panel. In our analysis pipeline, .fastq files are used for alignment and variant calling in Isaac Enrichment, Burrows-Wheeler Aligner (BWA) Enrichment, and NextGENe software, and .vcf files are then imported to GeneticistAssistant for variant filtering. Supervised analysis of filtered variants will allow the identification of disease-associated variants and/or of pathogenic variants associated with cancer predisposing syndromes outside the clinical context (incidental finding), with both being supported (if needed) by visual inspection of .bam files in Golden Helix GenomeBrowse (GB). Variants called because <t>of</t> <t>sequencing</t> errors are discarded on visual inspection of .bam files in Golden Helix GB. 1000G, 1000 Genomes Project; ACMG, American College of Med- ical Genetics and Genomics; Alt.var.freq., percentage of reads with alter- native allele; CDS, coding sequence; EVS, Exome Variant Server; ExAC, Exome Aggregation Consortium; In-house freq., variant frequency among all of the samples in our in-house database; MAF, minor allele frequency.
Library 186 Concentration, supplied by Illumina Inc, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rapid/10__1039_slash_c8en00071a-125-22-32?v=Illumina+Inc
Average 95 stars, based on 1 article reviews
library 186 concentration - by Bioz Stars, 2026-08
95/100 stars
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Image Search Results


Figure 4 Pipeline analysis for targeted NGS of multiple inherited cancer syndromes using the TruSight Cancer panel. In our analysis pipeline, .fastq files are used for alignment and variant calling in Isaac Enrichment, Burrows-Wheeler Aligner (BWA) Enrichment, and NextGENe software, and .vcf files are then imported to GeneticistAssistant for variant filtering. Supervised analysis of filtered variants will allow the identification of disease-associated variants and/or of pathogenic variants associated with cancer predisposing syndromes outside the clinical context (incidental finding), with both being supported (if needed) by visual inspection of .bam files in Golden Helix GenomeBrowse (GB). Variants called because of sequencing errors are discarded on visual inspection of .bam files in Golden Helix GB. 1000G, 1000 Genomes Project; ACMG, American College of Med- ical Genetics and Genomics; Alt.var.freq., percentage of reads with alter- native allele; CDS, coding sequence; EVS, Exome Variant Server; ExAC, Exome Aggregation Consortium; In-house freq., variant frequency among all of the samples in our in-house database; MAF, minor allele frequency.

Journal: The Journal of molecular diagnostics : JMD

Article Title: Validation of a Next-Generation Sequencing Pipeline for the Molecular Diagnosis of Multiple Inherited Cancer Predisposing Syndromes.

doi: 10.1016/j.jmoldx.2017.05.001

Figure Lengend Snippet: Figure 4 Pipeline analysis for targeted NGS of multiple inherited cancer syndromes using the TruSight Cancer panel. In our analysis pipeline, .fastq files are used for alignment and variant calling in Isaac Enrichment, Burrows-Wheeler Aligner (BWA) Enrichment, and NextGENe software, and .vcf files are then imported to GeneticistAssistant for variant filtering. Supervised analysis of filtered variants will allow the identification of disease-associated variants and/or of pathogenic variants associated with cancer predisposing syndromes outside the clinical context (incidental finding), with both being supported (if needed) by visual inspection of .bam files in Golden Helix GenomeBrowse (GB). Variants called because of sequencing errors are discarded on visual inspection of .bam files in Golden Helix GB. 1000G, 1000 Genomes Project; ACMG, American College of Med- ical Genetics and Genomics; Alt.var.freq., percentage of reads with alter- native allele; CDS, coding sequence; EVS, Exome Variant Server; ExAC, Exome Aggregation Consortium; In-house freq., variant frequency among all of the samples in our in-house database; MAF, minor allele frequency.

Article Snippet: Library Preparation and Sequencing For library preparation, we followed the manufacturer’s instructions (TruSight Rapid Capture Kit; Illumina Inc., San Diego, CA).

Techniques: Variant Assay, Software, Sequencing