mutation surveyor software v5.1.0 (SoftGenetics)
90
Structured Review
SoftGenetics
mutation surveyor software v5.1.0
Mutation Surveyor Software V5.1.0, 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/mutation+surveyor+software+v5%2E1%2E0/mutation+surveyor+software/pm36165864-82-4-8
Average 90 stars, based on 1 article reviews
Mutation Surveyor Software V5.1.0, 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/mutation+surveyor+software+v5%2E1%2E0/mutation+surveyor+software/pm36165864-82-4-8
Average 90 stars, based on 1 article reviews
mutation surveyor software v5.1.0 - by Bioz Stars,
2026-09
90/100 stars
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Mutagenesis:Article Title: Targeted molecular profiling of epithelial ovarian cancer from Italian BRCA wild-type patients with a BRCA and PARP pathways gene panel. Article Snippet: Ovarian cancer (OC) is the fifth most common type of cancer in women and the fourth most common cause of cancer death in women.. Identification of pathogenic variants in OC tissues has an important clinical significance for therapeutic and prevention purposes.. This study aims to evaluate the mutational profile of a patient cohort, negative for BRCA1/2 germinal variants and Mismatch Repair defects, using next-generation sequencing (NGS) approach on DNA from formalin-fixed paraffin-embedded samples. Article Title: Case Report: Male Lobular Breast Cancer in Hereditary Cancer Syndromes Article Snippet: Sequences were analyzed by Software:Article Title: Targeted molecular profiling of epithelial ovarian cancer from Italian BRCA wild-type patients with a BRCA and PARP pathways gene panel. Article Snippet: Ovarian cancer (OC) is the fifth most common type of cancer in women and the fourth most common cause of cancer death in women.. Identification of pathogenic variants in OC tissues has an important clinical significance for therapeutic and prevention purposes.. This study aims to evaluate the mutational profile of a patient cohort, negative for BRCA1/2 germinal variants and Mismatch Repair defects, using next-generation sequencing (NGS) approach on DNA from formalin-fixed paraffin-embedded samples. Article Title: Case Report: Male Lobular Breast Cancer in Hereditary Cancer Syndromes Article Snippet: Sequences were analyzed by |