Personalized copy number and segmental duplication maps using next-generation sequencing

Cited by (749)

Items 701–749 of 749

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  24. Additional file 1 of Hierarchical discovery of large-scale and focal copy number alterations in low-coverage cancer genomes
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  25. Additional file 4 of CHESS 3: an improved, comprehensive catalog of human genes and transcripts based on large-scale expression data, phylogenetic analysis, and protein structure
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  28. Additional file 2 of Technology dictates algorithms: recent developments in read alignment
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  29. Additional file 1 of Distinct structural variants and repeat landscape shape the genomes of the ancient grapes Aglianico and Falanghina
    Riccardo Aversano, Marina Iovene, Esposito, Salvatore, Alberto L’Abbate, Clizia Villano, Ermanno Di Serio, Cardone, Maria Francesca, Carlo Bergamini, Cigliano, Riccardo Aiese, Vincenzo D’Amelia et al. · 2024 · Figshare
  30. Additional file 2 of Pattern matching for high precision detection of LINE-1s in human genomes
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  31. Additional file 2 of CHOP: haplotype-aware path indexing in population graphs
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  32. Additional file 1 of VALOR2: characterization of large-scale structural variants using linked-reads
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  33. Additional file 2 of VALOR2: characterization of large-scale structural variants using linked-reads
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  34. Additional file 3 of Distinct structural variants and repeat landscape shape the genomes of the ancient grapes Aglianico and Falanghina
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  36. Additional file 2 of CHESS 3: an improved, comprehensive catalog of human genes and transcripts based on large-scale expression data, phylogenetic analysis, and protein structure
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  37. Additional file 1 of HATCHet2: clone- and haplotype-specific copy number inference from bulk tumor sequencing data
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  38. Additional file 2 of Genomic reproducibility in the bioinformatics era
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  39. Additional file 4 of Detecting copy number variation in next generation sequencing data from diagnostic gene panels
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