igv software (integrative genome viewer, 2013) (Broad Institute Inc)
90
Structured Review
Broad Institute Inc
igv software (integrative genome viewer, 2013)
Igv Software (Integrative Genome Viewer, 2013), 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/igv+software+(integrative+genome+viewer%2C+2013)/igv+software/pmc11250510-81-19-25
Average 90 stars, based on 1 article reviews
Igv Software (Integrative Genome Viewer, 2013), 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/igv+software+(integrative+genome+viewer%2C+2013)/igv+software/pmc11250510-81-19-25
Average 90 stars, based on 1 article reviews
igv software (integrative genome viewer, 2013) - by Bioz Stars,
2026-09
90/100 stars
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Software:Article Title: Clinical and genetic features of dominant Essential Tremor in Tuscany, Italy: FUS, CAMTA1, ATXN1 and beyond. Article Snippet: Objective: Essential Tremor (ET) is one of the most common neurological disorders.. In most instances ET is inherited as an autosomal dominant trait with age-related penetrance (virtually complete in advanced age); however, ET genetics remains elusive.. The current study aims to identify possibly pathogenic genetic variants in a group of well-characterized ET families. Article Title: Prospective genetic germline evaluation in a consecutive group of adult patients aged <60 years with myelodysplastic syndromes Article Snippet: .. Reads were aligned to the reference genome Grch37 (hg19) using Burrows‐Wheeler Aligner (BWA) tool, mapped and analyzed with the Article Title: Clinical and Genetic Characterization of Patients with Bartter and Gitelman Syndrome Article Snippet: Libraries were hybridized to the whole-exome capture arrays (SeqCap EZ Exome v3, Nimblegen, Roche, Basel, Switzerland) and sequenced with NextSeq500/550 (Illumina Inc., San Diego, CA, USA). .. The reads were aligned with the human reference hg19 genome using Burrows-Wheeler Aligner (BWA)), mapped and analyzed with the |