integrative genomics viewer version 2.18.4 software (Broad Institute Inc)
90
Structured Review
Broad Institute Inc
integrative genomics viewer version 2.18.4 software
Integrative Genomics Viewer Version 2.18.4 Software, supplied by Broad Institute 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/integrative+genomics+viewer+version+2%2E18%2E4+software/integrative+genomics+viewer/pmc11609615-89-10-16
Average 90 stars, based on 1 article reviews
Integrative Genomics Viewer Version 2.18.4 Software, supplied by Broad Institute 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/integrative+genomics+viewer+version+2%2E18%2E4+software/integrative+genomics+viewer/pmc11609615-89-10-16
Average 90 stars, based on 1 article reviews
integrative genomics viewer version 2.18.4 software - by Bioz Stars,
2026-10
90/100 stars
Images
Related Articles
Generated:Article Title: Diagnosis of acute Q fever using targeted next‑generation sequencing: A case report Article Snippet: The genomic alignment maps ( and ) were generated using Integrative Genomics Viewer version 2.18.4 software (Broad Institute), which is commonly used for visualizing sequencing data aligned to a reference genome. Software:Article Title: Diagnosis of acute Q fever using targeted next‑generation sequencing: A case report Article Snippet: The genomic alignment maps ( and ) were generated using Integrative Genomics Viewer version 2.18.4 software (Broad Institute), which is commonly used for visualizing sequencing data aligned to a reference genome. Sequencing:Article Title: Diagnosis of acute Q fever using targeted next‑generation sequencing: A case report Article Snippet: The genomic alignment maps ( and ) were generated using Integrative Genomics Viewer version 2.18.4 software (Broad Institute), which is commonly used for visualizing sequencing data aligned to a reference genome. |