Pages that link to "Q39174818"
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The following pages link to Whole-Genome Sequencing of Cytogenetically Balanced Chromosome Translocations Identifies Potentially Pathological Gene Disruptions and Highlights the Importance of Microhomology in the Mechanism of Formation (Q39174818):
Displaying 20 items.
- TIDDIT, an efficient and comprehensive structural variant caller for massive parallel sequencing data. (Q38637936) (← links)
- Identification of balanced chromosomal rearrangements previously unknown among participants in the 1000 Genomes Project: implications for interpretation of structural variation in genomes and the future of clinical cytogenetics (Q47863674) (← links)
- Phenotypic interpretation of complex chromosomal rearrangements informed by nucleotide-level resolution and structural organization of chromatin (Q48266844) (← links)
- Balanced Chromosomal Rearrangement Detection by Low-Pass Whole-Genome Sequencing (Q49823734) (← links)
- High-resolution detection of chromosomal rearrangements in leukemias through mate pair whole genome sequencing (Q52359182) (← links)
- De novo unbalanced translocations have a complex history/aetiology (Q57055693) (← links)
- Copy number variant and runs of homozygosity detection by microarrays enabled more precise molecular diagnoses in 11,020 clinical exome cases (Q64052555) (← links)
- Comprehensive structural variation genome map of individuals carrying complex chromosomal rearrangements (Q64234563) (← links)
- Induction of Chromosomal Translocations with CRISPR-Cas9 and Other Nucleases: Understanding the Repair Mechanisms That Give Rise to Translocations (Q64389376) (← links)
- Epigenetic maintenance of topological domains in the highly rearranged gibbon genome (Q89143203) (← links)
- Analysis of balanced reciprocal translocations in patients with subfertility using single-molecule optical mapping (Q89565261) (← links)
- Whole-genome sequencing reveals complex chromosome rearrangement disrupting NIPBL in infant with Cornelia de Lange syndrome (Q89990342) (← links)
- Breakpoint mapping at nucleotide resolution in X-autosome balanced translocations associated with clinical phenotypes (Q91283855) (← links)
- 2018 Victor A. McKusick Leadership Award: Molecular Mechanisms for Genomic and Chromosomal Rearrangements (Q92229368) (← links)
- Development of coupling controlled polymerizations by adapter-ligation in mate-pair sequencing for detection of various genomic variants in one single assay (Q92581348) (← links)
- Genome sequencing in cytogenetics: Comparison of short-read and linked-read approaches for germline structural variant detection and characterization (Q92961199) (← links)
- Whole-genome mate-pair sequencing of apparently balanced chromosome rearrangements reveals complex structural variations: two case studies (Q94545709) (← links)
- Whole Genome Low-Coverage Sequencing Concurrently Detecting Copy Number Variations and Their Underlying Complex Chromosomal Rearrangements by Systematic Breakpoint Mapping in Intellectual Deficiency/Developmental Delay Patients (Q98177815) (← links)
- Cytogenetically visible inversions are formed by multiple molecular mechanisms (Q99243096) (← links)
- Resolving Breakpoints of Chromosomal Rearrangements at the Nucleotide Level Using Sanger Sequencing (Q104584578) (← links)