splice prediction algorithms splicesitefinder-like (Interactive Biosoftware)
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Interactive Biosoftware
splice prediction algorithms splicesitefinder-like
Splice Prediction Algorithms Splicesitefinder Like, supplied by Interactive Biosoftware, 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/splice+prediction+algorithms+splicesitefinder-like/splice+prediction+algorithms+splicesitefinder+like/pm35802266-49-13-64
Average 90 stars, based on 1 article reviews
Splice Prediction Algorithms Splicesitefinder Like, supplied by Interactive Biosoftware, 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/splice+prediction+algorithms+splicesitefinder-like/splice+prediction+algorithms+splicesitefinder+like/pm35802266-49-13-64
Average 90 stars, based on 1 article reviews
splice prediction algorithms splicesitefinder-like - by Bioz Stars,
2026-10
90/100 stars
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other:Article Title: Prevalence and spectrum of MLH1 , MSH2 , and MSH6 pathogenic germline variants in Pakistani colorectal cancer patients Article Snippet: Furthermore, all novel and previously reported intronic VUS in MMR genes were analyzed for their potential effect on splicing using the splice prediction algorithms SpliceSiteFinder-like (http:// www.umd.be/searchSpliceSite.html ), MaxEntScan ( http://genes.mit.edu/burgelab/maxent/Xmaxentscan_scoreseq.html ), NNSPLICE ( http://www.fruitfly.org/seq_tools/splice.html ), GeneSplicer ( http://www.ccb.jhu.edu/software/genesplicer/ ) and HumanSpliceFinder ( http://www.umd.be/HSF3/ ) via the Article Title: Prevalence of FANCM germline variants in BRCA1/2 negative breast and/or ovarian cancer patients from Pakistan. Article Snippet: The Fanconi anemia complementation group M (FANCM) gene is a potential candidate for breast/ovarian cancer susceptibility in European populations.. Here, we examined the contribution of FANCM germline variants to hereditary breast and/or ovarian cancer in Pakistan.. Comprehensive FANCM variant screening was performed in 201 BRCA1 and BRCA2 (BRCA1/2) negative Pakistani patients with and without triple-negative breast cancer (TNBC) and/or ovarian cancer, using denaturing high-performance liquid chromatography analysis (DHPLC) followed by DNA sequencing. Article Title: Deleterious RAD51C germline mutations rarely predispose to breast and ovarian cancer in Pakistan. Article Snippet: RAD51C plays a key role in homologous recombination-mediated DNA repair and maintenance of genomic stability.. Biallelic RAD51C mutations cause Fanconi anemia, and monoallelic mutations predispose women to breast and ovarian cancer.. Genetic variability of RAD51C and its impact in Asian populations have been poorly studied. |