solve software v3.6 (BioNano Genomics)
90
Structured Review
BioNano Genomics
solve software v3.6
Solve Software V3.6, supplied by BioNano Genomics, 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/solve+software+v3%2E6/solve+software+v3+6/pmc11390914-206-11-10
Average 90 stars, based on 1 article reviews
Solve Software V3.6, supplied by BioNano Genomics, 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/solve+software+v3%2E6/solve+software+v3+6/pmc11390914-206-11-10
Average 90 stars, based on 1 article reviews
solve software v3.6 - by Bioz Stars,
2026-09
90/100 stars
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Variant Assay:Article Title: Deep Intronic LINE-1 Insertions in NF1 : Expanding the Spectrum of Neurofibromatosis Type 1-Associated Rearrangements. Article Snippet: The de novo assembly and Variant Annotation Pipeline were executed on Article Title: A reference genome for the Harpy Eagle reveals steady demographic decline and chromosomal rearrangements in the origin of Accipitriformes Article Snippet: For the first step, the optical map was fed into Article Title: A Case of CDKL5 Deficiency Due to an X Chromosome Pericentric Inversion: Delineation of Structural Rearrangements as an Overlooked Recurrent Pathological Mechanism Article Snippet: The de novo assembly and variant annotation pipeline were executed on Article Title: PATZ1-Rearranged Tumors of the Central Nervous System: Characterization of a Pediatric Series of Seven Cases. Article Snippet: PATZ1-rearranged sarcomas are well-recognized tumors as part of the family of round cell sarcoma with EWSR1-non-ETS fusions.. Whether PATZ1-rearranged central nervous system (CNS) tumors are a distinct tumor type is debatable.. We thoroughly characterized a pediatric series of PATZ1-rearranged CNS tumors by chromosome microarray analysis (CMA), DNA methylation analysis, gene expression profiling and, when frozen tissue is available, optical genome mapping (OGM). Article Title: Intragenic inversions in NF1 gene as pathogenic mechanism in neurofibromatosis type 1. Article Snippet: The de novo assembly and Variant Annotation Pipeline were executed on Article Title: A Case of CDKL5 Deficiency Due to an X Chromosome Pericentric Inversion: Delineation of Structural Rearrangements as an Overlooked Recurrent Pathological Mechanism. Article Snippet: The de novo assembly and variant annotation pipeline were executed on Article Title: Structural rearrangements as a recurrent pathogenic mechanism for SETBP1 haploinsufficiency Article Snippet: The de novo assembly and Variant Annotation Pipeline were executed on Software:Article Title: Deep Intronic LINE-1 Insertions in NF1 : Expanding the Spectrum of Neurofibromatosis Type 1-Associated Rearrangements. Article Snippet: The de novo assembly and Variant Annotation Pipeline were executed on Article Title: A reference genome for the Harpy Eagle reveals steady demographic decline and chromosomal rearrangements in the origin of Accipitriformes Article Snippet: For the first step, the optical map was fed into Article Title: A Case of CDKL5 Deficiency Due to an X Chromosome Pericentric Inversion: Delineation of Structural Rearrangements as an Overlooked Recurrent Pathological Mechanism Article Snippet: The de novo assembly and variant annotation pipeline were executed on Article Title: PATZ1-Rearranged Tumors of the Central Nervous System: Characterization of a Pediatric Series of Seven Cases. Article Snippet: PATZ1-rearranged sarcomas are well-recognized tumors as part of the family of round cell sarcoma with EWSR1-non-ETS fusions.. Whether PATZ1-rearranged central nervous system (CNS) tumors are a distinct tumor type is debatable.. We thoroughly characterized a pediatric series of PATZ1-rearranged CNS tumors by chromosome microarray analysis (CMA), DNA methylation analysis, gene expression profiling and, when frozen tissue is available, optical genome mapping (OGM). Article Title: Intragenic inversions in NF1 gene as pathogenic mechanism in neurofibromatosis type 1. Article Snippet: The de novo assembly and Variant Annotation Pipeline were executed on Article Title: A Case of CDKL5 Deficiency Due to an X Chromosome Pericentric Inversion: Delineation of Structural Rearrangements as an Overlooked Recurrent Pathological Mechanism. Article Snippet: The de novo assembly and variant annotation pipeline were executed on Article Title: Structural rearrangements as a recurrent pathogenic mechanism for SETBP1 haploinsufficiency Article Snippet: The de novo assembly and Variant Annotation Pipeline were executed on |